- Approval Id
- 398021527df2c6d9
- Drug Approval Emc Name
- Posaconazole Amarox 100 mg gastro-resistant tablets
- Drug Name
- Posaconazole Amarox 100 mg gastro-resistant tablets
- Company Name
- Amarox Limited
- Company Address
- Congress House, 3rd Floor, 14 Lyon Road, Harrow
- Company Website
- https://amaroxpharma.co.uk/
- Company Telephone
- +44(0)20397 20002
- Company Medical Info Direct Line
- +44(0)20397 20005
- Company Medical Info Email
- amarox_micc@mitoconbiopharma.com
- Company Customer Care Direct Line
- +44(0)20397 20002
- Atc Code
- J02AC04
- Legal Category
- Prescription only medicine
- Authorisation Holder
- Amarox Limited
Congress House, 14 Lyon Road
Harrow, HA1 2EN
United Kingdom
- Authorisation Number
- PL 49445/0151
- Authorisation Date
- 04/06/2024
- Instruction Authorisation Holder
- Amarox Limited
Congress House, 14 Lyon Road
Harrow, HA1 2EN
United Kingdom
- Instruction Authorisation Number
- PL 49445/0151
- Instruction Authorisation Date
- 04/06/2024
- Instruction Composition
- Each gastro-resistant tablet contains 100 mg of posaconazole.
For the full list of excipients, see section 6.1.
- Instruction Dosage Form
- Gastro-resistant tablet.
Light orange, oblong shaped, film-coated tablets with approx. dimensions of 17.50 mm X 6.80 mm de-bossed with "H" on one side and "P11" on the other side.
- Instruction Clinical Particulars
- 4.1 Therapeutic indications
Posaconazole Amarox gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4.2 and 5.1):
- Invasive aspergillosis
Posaconazole Amarox gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4.2 and 5.1):
- Invasive aspergillosis in patients with disease that is refractory to amphotericin B or itraconazole or in patients who are intolerant of these medicinal products;
- Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B;
- Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;
- Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products.
Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy.
Posaconazole Amarox gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4.2 and 5.1):
- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high-risk of developing invasive fungal infections;
- Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high- dose immunosuppressive therapy for graft versus host disease and who are at high-risk of developing invasive fungal infections.
Please refer to the Summary of Product Characteristics of posaconazole oral suspension for use in oropharyngeal candidiasis.4.2 Posology and method of administration
Treatment should be initiated by a physician experienced in the management of fungal infections or in the supportive care of high-risk patients for which posaconazole is indicated as prophylaxis.
\*\*Non-interchangeability between posaconazole Amarox tablets and posaconazole oral suspension\*\*
The tablet is not to be used interchangeably with the oral suspension due to the differences between these two formulations in frequency of dosing, administration with food and plasma drug concentration achieved. Therefore, follow the specific dose recommendations for each formulation.
\*\*Posology\*\*
Posaconazole is also available as 40 mg/mL oral suspension, 300 mg concentrate for solution for infusion and 300 mg gastro-resistant powder and solvent for oral suspension. Posaconazole tablets generally provide higher plasma drug exposures than posaconazole oral suspension under both fed and fasted conditions. Therefore, the tablets are the preferred formulation to optimise plasma concentrations.
Recommended dose in paediatric patients from 2 years of age weighing more than 40 kg and in adults is shown in Table 1.
Posaconazole Amarox gastro-resistant powder and solvent for oral suspension is recommended for oral use in paediatric patients 2 years of age and older weighing 40 kg or less. Refer to the gastro-resistant powder and solvent for oral suspension SmPC for additional dosing information.
\*\*Table 1.\*\* Recommended dose in paediatric patients from 2 years of age weighing more than 40 kg and in adults according to indication
| | |
| --- | --- |
| \*\*Indication\*\* | \*\*Dose and duration of therapy\*\* (See section 5.2) |
| Treatment of invasive aspergillosis (only for adults) | Loading dose of 300 mg (three 100 mg tablets or 300 mg concentrate for solution for infusion) twice a day on the first day, then 300 mg (three 100 mg tablets or 300 mg concentrate for solution for infusion) once a day thereafter. Each tablet dose may be taken without regard to food intake. Recommended total duration of therapy is 6-12 weeks. Switching between intravenous and oral administration is appropriate when clinically indicated. |
| Refractory invasive fungal infections (IFI)/patients with IFI intolerant to 1st line therapy | Loading dose of 300 mg (three 100 mg tablets) twice a day on the first day, then 300 mg (three 100 mg tablets) once a day thereafter. Each dose may be taken without regard to food intake. Duration of therapy should be based on the severity of the underlying disease, recovery from immunosuppression, and clinical response. |
| Prophylaxis of invasive fungal infections | Loading dose of 300 mg (three 100 mg tablets) twice a day on the first day, then 300 mg (three 100 mg tablets) once a day thereafter. Each dose may be taken without regard to food intake. Duration of therapy is based on recovery from neutropenia or immunosuppression. For patients with acute myelogenous leukaemia or myelodysplastic syndromes, prophylaxis with posaconazole should start several days before the anticipated onset of neutropenia and continue for 7 days after the neutrophil count rises above 500 cells per mm3. |
\*\*Special populations\*\*
\*Renal impairment\*
An effect of renal impairment on the pharmacokinetics of posaconazole is not expected and no dose adjustment is recommended (see section 5.2).
\*Hepatic impairment\*
Limited data on the effect of hepatic impairment (including Child-Pugh C classification of chronic liver disease) on the pharmacokinetics of posaconazole demonstrate an increase in plasma exposure compared to subjects with normal hepatic function, but do not suggest that dose adjustment is necessary (see sections 4.4 and 5.2). It is recommended to exercise caution due to the potential for higher plasma exposure.
\*Paediatric population\*
The safety and efficacy of posaconazole in children aged below 2 years have not been established.
No clinical data are available.
\*\*Method of administration\*\*
For oral use
Posaconazole Amarox gastro-resistant tablets may be taken with or without food (see section 5.2). The tablets should be swallowed whole with water and should not be crushed, chewed, or broken.4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Co-administration with ergot alkaloids (see section 4.5).
Co-administration with the CYP3A4 substrates terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine since this may result in increased plasma concentrations of these medicinal products, leading to QTc prolongation and rare occurrences of torsades de pointes (see sections 4.4 and 4.5).
Co-administration with the HMG-CoA reductase inhibitors simvastatin, lovastatin and atorvastatin (see section 4.5).
Co-administration during the initiation and dose-titration phase of venetoclax in Chronic Lymphocytic Leukaemia (CLL) patients (see sections 4.4 and 4.5).4.4 Special warnings and precautions for use
\*\*Hypersensitivity\*\*
There is no information regarding cross-sensitivity between posaconazole and other azole antifungal agents. Caution should be used when prescribing posaconazole to patients with hypersensitivity to other azoles.
\*\*Hepatic toxicity\*\*
Hepatic reactions (e.g. mild to moderate elevations in ALT, AST, alkaline phosphatase, total bilirubin and/or clinical hepatitis) have been reported during treatment with posaconazole. Elevated liver function tests were generally reversible on discontinuation of therapy and in some instances these tests normalised without interruption of therapy. Rarely, more severe hepatic reactions with fatal outcomes have been reported.
Posaconazole should be used with caution in patients with hepatic impairment due to limited clinical experience and the possibility that posaconazole plasma levels may be higher in these patients (see sections 4.2 and 5.2).
\*\*Monitoring of hepatic function\*\*
Liver function tests should be evaluated at the start of and during the course of posaconazole therapy. Patients who develop abnormal liver function tests during posaconazole therapy must be routinely monitored for the development of more severe hepatic injury. Patient management should include laboratory evaluation of hepatic function (particularly liver function tests and bilirubin).
Discontinuation of posaconazole should be considered if clinical signs and symptoms are consistent with development of liver disease.
\*\*QTc prolongation\*\*
Some azoles have been associated with prolongation of the QTc interval. Posaconazole must not be administered with medicinal products that are substrates for CYP3A4 and are known to prolong the QTc interval (see sections 4.3 and 4.5). Posaconazole should be administered with caution to patients with pro-arrhythmic conditions such as:
• Congenital or acquired QTc prolongation
• Cardiomyopathy, especially in the presence of cardiac failure
• Sinus bradycardia
• Existing symptomatic arrhythmias
• Concomitant use with medicinal products known to prolong the QTc interval (other than those mentioned in section 4.3).
Electrolyte disturbances, especially those involving potassium, magnesium or calcium levels, should be monitored and corrected as necessary before and during posaconazole therapy.
\*\*Drug interactions\*\*
Posaconazole is an inhibitor of CYP3A4 and should only be used under specific circumstances during treatment with other medicinal products that are metabolised by CYP3A4 (see section 4.5).
\*\*Midazolam and other benzodiazepines\*\*
Due to the risk of prolonged sedation and possible respiratory depression co- administration of posaconazole with any benzodiazepines metabolised by CYP3A4 (e.g. midazolam, triazolam, alprazolam) should only be considered if clearly necessary. Dose adjustment of benzodiazepines metabolised by CYP3A4 should be considered (see section 4.5).
\*\*Vincristine toxicity\*\*
Concomitant administration of azole antifungals, including posaconazole, with vincristine has been associated with neurotoxicity and other serious adverse reactions, including seizures, peripheral neuropathy, syndrome of inappropriate antidiuretic hormone secretion, and paralytic ileus. Reserve azole antifungals, including posaconazole, for patients receiving a vinca alkaloid, including vincristine, who have no alternative antifungal treatment options (see section 4.5).
\*\*Venetoclax toxicity\*\*
Concomitant administration of strong CYP3A inhibitors, including posaconazole, with the CYP3A4 substrate venetoclax, may increase venetoclax toxicities, including the risk of tumour lysis syndrome (TLS) and neutropenia (see sections 4.3 and 4.5). Refer to the venetoclax SmPC for detailed guidance.
\*\*Rifamycin antibacterials (rifampicin, rifabutin), flucloxacillin, certain anticonvulsants (phenytoin, carbamazepine, phenobarbital, primidone), and efavirenz.\*\*
Posaconazole concentrations may be significantly lowered in combination; therefore, concomitant use with posaconazole should be avoided unless the benefit to the patient outweighs the risk (see section 4.5).
\*\*Plasma exposure\*\*
Posaconazole plasma concentrations following administration of posaconazole tablets are generally higher than those obtained with posaconazole oral suspension. Posaconazole plasma concentrations following administration of posaconazole tablets may increase over time in some patients (see section 5.2).
\*\*Gastrointestinal dysfunction\*\*
There are limited pharmacokinetic data in patients with severe gastrointestinal dysfunction (such as severe diarrhoea). Patients who have severe diarrhoea or vomiting should be monitored closely for breakthrough fungal infections.
\*\*Photosensitivity reaction\*\*
Posaconazole may cause increased risk of photosensitivity reaction. Patients should be advised to avoid sun exposure during treatment without adequate protection such as protective clothing and sunscreen with a high sun protection factor (SPF).
\*\*Sodium\*\*
This medicinal product contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially 'sodium-free'.4.5 Interaction with other medicinal products and other forms of interaction
\*\*Effects of other medicinal products on posaconazole\*\*
Posaconazole is metabolised via UDP glucuronidation (phase 2 enzymes) and is a substrate for p-glycoprotein (P-gp) efflux \*in vitro\*. Therefore, inhibitors (e.g. verapamil, ciclosporin, quinidine, clarithromycin, erythromycin, etc.) or inducers (e.g. rifampicin, rifabutin, certain anticonvulsants, etc.) of these clearance pathways may increase or decrease posaconazole plasma concentrations, respectively.
\*Rifabutin\*
Rifabutin (300 mg once a day) decreased the Cmax (maximum plasma concentration) and AUC (area under the plasma concentration time curve) of posaconazole to 57 % and 51 %, respectively. Concomitant use of posaconazole and rifabutin and similar inducers (e.g. rifampicin) should be avoided unless the benefit to the patient outweighs the risk. See also below regarding the effect of posaconazole on rifabutin plasma levels.
\*\*Flucloxacillin\*\*
Flucloxacillin (a CYP450 inducer) may decrease plasma posaconazole concentrations. Concomitant use of posaconazole and flucloxacillin should be avoided unless the benefit to the patient outweighs the risk (see section 4.4).
\*Efavirenz\*
Efavirenz (400 mg once a day) decreased the Cmax and AUC of posaconazole by 45 % and 50 %, respectively. Concomitant use of posaconazole and efavirenz should be avoided unless the benefit to the patient outweighs the risk.
\*Fosamprenavir\*
Combining fosamprenavir with posaconazole may lead to decreased posaconazole plasma concentrations. If concomitant administration is required, close monitoring for breakthrough fungal infections is recommended. Repeat dose administration of fosamprenavir (700 mg twice daily x 10 days) decreased the Cmax and AUC of posaconazole oral suspension (200 mg once daily on the 1st day, 200 mg twice daily on the 2nd day, then 400 mg twice daily x 8 Days) by 21 % and 23 %, respectively. The effect of posaconazole on fosamprenavir levels when fosamprenavir is given with ritonavir is unknown.
\*Phenytoin\*
Phenytoin (200 mg once a day) decreased the Cmax and AUC of posaconazole by 41 % and 50 %, respectively. Concomitant use of posaconazole and phenytoin and similar inducers (e.g. carbamazepine, phenobarbital, primidone) should be avoided unless the benefit to the patient outweighs the risk.
\*H2 receptor antagonists and proton pump inhibitors\*
No clinically relevant effects were observed when posaconazole tablets are concomitantly used with antacids, H2-receptor antagonists and proton pump inhibitors. No dose adjustment of posaconazole tablets is required when posaconazole tablets are concomitantly used with antacids, H2-receptor antagonists and proton pump inhibitors.
\*\*Effects of posaconazole on other medicinal products\*\*
Posaconazole is a potent inhibitor of CYP3A4. Co-administration of posaconazole with CYP3A4 substrates may result in large increases in exposure to CYP3A4 substrates as exemplified by the effects on tacrolimus, sirolimus, atazanavir and midazolam below. Caution is advised during co- administration of posaconazole with CYP3A4 substrates administered intravenously and the dose of the CYP3A4 substrate may need to be reduced. If posaconazole is used concomitantly with CYP3A4 substrates that are administered orally, and for which an increase in plasma concentrations may be associated with unacceptable adverse reactions, plasma concentrations of the CYP3A4 substrate and/or adverse reactions should be closely monitored and the dose adjusted as needed. Several of the interaction studies were conducted in healthy volunteers in whom a higher exposure to posaconazole occurs compared to patients administered the same dose. The effect of posaconazole on CYP3A4 substrates in patients might be somewhat lower than that observed in healthy volunteers, and is expected to be variable between patients due to the variable posaconazole exposure in patients. The effect of co-administration with posaconazole on plasma levels of CYP3A4 substrates may also be variable within a patient.
\*Terfenadine, astemizole, cisapride, pimozide, halofantrine and quinidine (CYP3A4 substrates)\*
Co-administration of posaconazole and terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine is contraindicated. Co-administration may result in increased plasma concentrations of these medicinal products, leading to QTc prolongation and rare occurrences of torsades de pointes (see section 4.3).
\*Ergot alkaloids\*
Posaconazole may increase the plasma concentration of ergot alkaloids (ergotamine and dihydroergotamine), which may lead to ergotism. Co- administration of posaconazole and ergot alkaloids is contraindicated (see section 4.3).
\*HMG-CoA reductase inhibitors metabolised through CYP3A4 (e.g. simvastatin, lovastatin, and atorvastatin)\*
Posaconazole may substantially increase plasma levels of HMG-CoA reductase inhibitors that are metabolised by CYP3A4. Treatment with these HMG-CoA reductase inhibitors should be discontinued during treatment with posaconazole as increased levels have been associated with rhabdomyolysis (see section 4.3).
\*Vinca alkaloids\*
Most of the vinca alkaloids (e.g. vincristine and vinblastine) are substrates of CYP3A4. Concomitant administration of azole antifungals, including posaconazole, with vincristine has been associated with serious adverse reactions (see section 4.4). Posaconazole may increase the plasma concentrations of vinca alkaloids which may lead to neurotoxicity and other serious adverse reactions. Therefore, reserve azole antifungals, including posaconazole, for patients receiving a vinca alkaloid, including vincristine, who have no alternative antifungal treatment options.
\*Rifabutin\*
Posaconazole increased the Cmax and AUC of rifabutin by 31 % and 72 %, respectively. Concomitant use of posaconazole and rifabutin should be avoided unless the benefit to the patient outweighs the risk (see also above regarding the effect of rifabutin on plasma levels of posaconazole). If these medicinal products are co-administered, careful monitoring of full blood counts and adverse reactions related to increased rifabutin levels (e.g. uveitis) is recommended.
\*Sirolimus\*
Repeat dose administration of posaconazole oral suspension (400 mg twice daily for 16 days) increased the Cmax and AUC of sirolimus (2 mg single dose) an average of 6.7-fold and 8.9-fold (range 3.1 to 17.5-fold), respectively, in healthy subjects. The effect of posaconazole on sirolimus in patients is unknown, but is expected to be variable due to the variable posaconazole exposure in patients. Co-administration of posaconazole with sirolimus is not recommended and should be avoided whenever possible. If it is considered that co-administration is unavoidable, then it is recommended that the dose of sirolimus should be greatly reduced at the time of initiation of posaconazole therapy and that there should be very frequent monitoring of trough concentrations of sirolimus in whole blood. Sirolimus concentrations should be measured upon initiation, during co-administration, and at discontinuation of posaconazole treatment, with sirolimus doses adjusted accordingly. It should be noted that the relationship between sirolimus trough concentration and AUC is changed during co-administration with posaconazole. As a result, sirolimus trough concentrations that fall within the usual therapeutic range may result in sub-therapeutic levels. Therefore, trough concentrations that fall in the upper part of the usual therapeutic range should be targeted and careful attention should be paid to clinical signs and symptoms, laboratory parameters and tissue biopsies.
\*Ciclosporin\*
In heart transplant patients on stable doses of ciclosporin, posaconazole oral suspension 200 mg once daily increased ciclosporin concentrations requiring dose reductions. Cases of elevated ciclosporin levels resulting in serious adverse reactions, including nephrotoxicity and one fatal case of leukoencephalopathy, were reported in clinical efficacy studies. When initiating treatment with posaconazole in patients already receiving ciclosporin, the dose of ciclosporin should be reduced (e.g. to about three quarters of the current dose). Thereafter blood levels of ciclosporin should be monitored carefully during co-administration, and upon discontinuation of posaconazole treatment, and the dose of ciclosporin should be adjusted as necessary.
\*Tacrolimus\*
Posaconazole increased Cmax and AUC of tacrolimus (0.05 mg/kg body weight single dose) by 121 % and 358 %, respectively. Clinically significant interactions resulting in hospitalisation and/or posaconazole discontinuation were reported in clinical efficacy studies. When initiating posaconazole treatment in patients already receiving tacrolimus, the dose of tacrolimus should be reduced (e.g. to about one third of the current dose). Thereafter blood levels of tacrolimus should be monitored carefully during co- administration, and upon discontinuation of posaconazole, and the dose of tacrolimus should be adjusted as necessary.
\*HIV Protease inhibitors\*
As HIV protease inhibitors are CYP3A4 substrates, it is expected that posaconazole will increase plasma levels of these antiretroviral agents. Following co-administration of posaconazole oral suspension (400 mg twice daily) with atazanavir (300 mg once daily) for 7 days in healthy subjects Cmax and AUC of atazanavir increased by an average of 2.6-fold and 3.7-fold (range 1.2 to 26-fold), respectively. Following co-administration of posaconazole oral suspension (400 mg twice daily) with atazanavir and ritonavir (300/100 mg once daily) for 7 days in healthy subjects Cmax and AUC of atazanavir increased by an average of 1.5-fold and 2.5-fold (range 0.9 to 4.1-fold), respectively. The addition of posaconazole to therapy with atazanavir or with atazanavir plus ritonavir was associated with increases in plasma bilirubin levels. Frequent monitoring for adverse reactions and toxicity related to antiretroviral agents that are substrates of CYP3A4 is recommended during co- administration with posaconazole.
\*Midazolam and other benzodiazepines metabolised by CYP3A4\*
In a study in healthy volunteers posaconazole oral suspension (200 mg once daily for 10 days) increased the exposure (AUC) of intravenous midazolam (0.05 mg/kg) by 83 %. In another study in healthy volunteers, repeat dose administration of posaconazole oral suspension (200 mg twice daily for 7 days) increased the Cmax and AUC of intravenous midazolam (0.4 mg single dose) by an average of 1.3- and 4.6-fold (range 1.7 to 6.4-fold), respectively; Posaconazole oral suspension 400 mg twice daily for 7 days increased the intravenous midazolam Cmax and AUC by 1.6 and 6.2-fold (range 1.6 to 7.6- fold), respectively. Both doses of posaconazole increased Cmax and AUC of oral midazolam (2 mg single oral dose) by 2.2 and 4.5-fold, respectively. In addition, posaconazole oral suspension (200 mg or 400 mg) prolonged the mean terminal half-life of midazolam from approximately 3-4 hours to 8-10 hours during co-administration.
Due to the risk of prolonged sedation it is recommended that dose adjustments should be considered when posaconazole is administered concomitantly with any benzodiazepine that is metabolised by CYP3A4 (e.g. midazolam, triazolam, alprazolam) (see section 4.4).
\*Calcium channel blockers metabolised through CYP3A4 (e.g. diltiazem, verapamil, nifedipine, nisoldipine)\*
Frequent monitoring for adverse reactions and toxicity related to calcium channel blockers is recommended during co-administration with posaconazole. Dose adjustment of calcium channel blockers may be required.
\*Digoxin\*
Administration of other azoles has been associated with increases in digoxin levels. Therefore, posaconazole may increase plasma concentration of digoxin and digoxin levels need to be monitored when initiating or discontinuing posaconazole treatment.
\*Sulfonylureas\*
Glucose concentrations decreased in some healthy volunteers when glipizide was co-administered with posaconazole. Monitoring of glucose concentrations is recommended in diabetic patients.
\*All-trans retinoic acid (ATRA) or tretinoin\*
As ATRA is metabolised by the hepatic CYP450 enzymes, notably CYP3A4, concomitant administration with posaconazole, which is a strong inhibitor of CYP3A4, may lead to increased exposure to tretinoin resulting in an increased toxicity (especially hypercalcaemia). Serum calcium levels should be monitored and, if needed, appropriate dose adjustments of tretinoin should be considered during the treatment with posaconazole, and during the following days after treatment.
\*Venetoclax\*
Compared with venetoclax 400 mg administered alone, co-administration of 300 mg posaconazole, a strong CYP3A inhibitor, with venetoclax 50 mg and 100 mg for 7 days in 12 patients, increased venetoclax Cmax to 1.6-fold and 1.9-fold, and AUC to 1.9-fold and 2.4-fold, respectively (see sections 4.3 and 4.4).
Refer to the venetoclax SmPC.
\*\*Paediatric population\*\*
Interaction studies have only been performed in adults.4.6 Fertility, pregnancy and lactation
\*\*Pregnancy\*\*
There is insufficient information on the use of posaconazole in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3). The potential risk for humans is unknown.
Women of childbearing potential have to use effective contraception during treatment. Posaconazole must not be used during pregnancy unless the benefit to the mother clearly outweighs the potential risk to the foetus.
\*\*Breast-feeding\*\*
Posaconazole is excreted into the milk of lactating rats (see section 5.3). The excretion of posaconazole in human breast milk has not been investigated.
Breast-feeding must be stopped on initiation of treatment with posaconazole.
\*\*Fertility\*\*
Posaconazole had no effect on fertility of male rats at doses up to 180 mg/kg (3.4 times the 300-mg tablet based on steady-state plasma concentrations in patients) or female rats at a dose up to 45 mg/kg (2.6 times the 300-mg tablet based on steady- state plasma concentrations in patients). There is no clinical experience assessing the impact of posaconazole on fertility in humans.4.7 Effects on ability to drive and use machines
Since certain adverse reactions (e.g. dizziness, somnolence, etc.) have been reported with posaconazole use, which potentially may affect driving/operating machinery, caution needs to be used.4.8 Undesirable effects
\*\*Summary of the safety profile\*\*
Safety data mainly derive from studies with the oral suspension.
The safety of posaconazole oral suspension has been assessed in > 2,400 patients and healthy volunteers enrolled in clinical studies and from post- marketing experience. The most frequently reported serious related adverse reactions included nausea, vomiting, diarrhoea, pyrexia, and increased bilirubin.
\*\*\*Posaconazole tablets\*\*\*
The safety of posaconazole tablet has been assessed in 104 healthy volunteers and 230 patients enrolled in a clinical study of antifungal prophylaxis.
The safety of posaconazole concentrate for solution for infusion and posaconazole tablet has been assessed in 288 patients enrolled in a clinical study of aspergillosis of whom 161 patients received the concentrate for solution for infusion and 127 patients received the tablet formulation.
The tablet formulation was investigated in AML and MDS patients and those after HSCT with or at risk for Graft versus Host Disease (GVHD) only.
Maximum duration of exposure to the tablet formulation was shorter than with the oral suspension. Plasma exposure resulting from the tablet formulation was higher than observed with the oral suspension.
The safety of posaconazole tablets has been assessed in 230 patients enrolled in the pivotal clinical study. Patients were enrolled in a non-comparative pharmacokinetic and safety study of posaconazole tablets when given as antifungal prophylaxis. Patients were immunocompromised with underlying conditions including haematological malignancy, neutropenia post- chemotherapy, GVHD, and post HSCT. Posaconazole therapy was given for a median duration of 28 days. Twenty patients received 200 mg daily dose and 210 patients received 300 mg daily dose (following twice daily dosing on Day 1 in each cohort).
The safety of posaconazole tablets and concentrate for solution for infusion were also investigated in a controlled study of treatment of invasive aspergillosis. The maximum duration of invasive aspergillosis treatment was similar to that studied with the oral suspension for salvage treatment and was longer than that with the tablets or concentrate for solution for infusion in prophylaxis.
\*\*Tabulated list of adverse reactions\*\*
Within the organ system classes, adverse reactions are listed under headings of frequency using the following categories: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥ 1/10,000 to <1/1,000); very rare (<1/10,000); not known (cannot be estimated from the available data).
\*\*Table 2.\*\* Adverse reactions by body system and frequency reported in clinical studies and/or post-marketing use\\*
| | |
| --- | --- |
| \*\*Blood and lymphatic system disorders\*\* | |
| Common: | neutropenia |
| Uncommon: | thrombocytopenia, leukopenia, anaemia, eosinophilia, lymphadenopathy, splenic infarction |
| Rare: | haemolytic uraemic syndrome, thrombotic thrombocytopenic purpura, pancytopenia, coagulopathy, haemorrhage |
| \*\*Immune system disorders\*\* | |
| Uncommon: | allergic reaction |
| Rare: | hypersensitivity reaction |
| \*\*Endocrine disorders\*\* | |
| Rare: | adrenal insufficiency, blood gonadotropin decreased, pseudoaldosteronism |
| \*\*Metabolism and nutrition disorders\*\* | |
| Common: | electrolyte imbalance, anorexia, decreased appetite, hypokalaemia, hypomagnesaemia |
| Uncommon: | hyperglycaemia, hypoglycaemia |
| \*\*Psychiatric disorders\*\* | |
| Uncommon: | abnormal dreams, confusional state, sleep disorder |
| Rare: | psychotic disorder, depression |
| \*\*Nervous system disorders\*\* | |
| Common: | paraesthesia, dizziness, somnolence, headache, dysgeusia |
| Uncommon: | convulsions, neuropathy, hypoaesthesia, tremor, aphasia, insomnia |
| Rare: | cerebrovascular accident, encephalopathy, peripheral neuropathy, syncope |
| \*\*Eye disorders\*\* | |
| Uncommon: | blurred vision, photophobia, visual acuity reduced |
| Rare: | diplopia, scotoma |
| \*\*Ear and labyrinth disorder\*\* | |
| Rare: | hearing impairment |
| \*\*Cardiac disorders\*\* | |
| Uncommon: | long QT syndrome§, electrocardiogram abnormal§, palpitations, bradycardia, supraventricular extrasystoles, tachycardia |
| Rare: | torsade de pointes, sudden death, ventricular tachycardia, cardio-respiratory arrest, cardiac failure, myocardial infarction |
| \*\*Vascular disorders\*\* | |
| Common: | hypertension |
| Uncommon: | hypotension, vasculitis |
| Rare: | pulmonary embolism, deep vein thrombosis |
| \*\*Respiratory, thoracic and mediastinal disorders\*\* | |
| Uncommon: | cough, epistaxis, hiccups, nasal congestion, pleuritic pain, tachypnoea |
| Rare: | pulmonary hypertension, interstitial pneumonia, pneumonitis |
| \*\*Gastrointestinal disorders\*\* | |
| Very Common: | nausea |
| Common: | vomiting, abdominal pain, diarrhoea, dyspepsia, dry mouth, flatulence, constipation, anorectal discomfort |
| Uncommon: | pancreatitis, abdominal distension, enteritis, epigastric discomfort, eructation, gastroesophageal reflux disease, oedema mouth |
| Rare: | gastrointestinal haemorrhage, ileus |
| \*\*Hepatobiliary disorders\*\* | |
| Common: | liver function tests raised (ALT increased, AST increased, bilirubin increased, alkaline phosphatase increased, GGT increased) |
| Uncommon: | hepatocellular damage, hepatitis, jaundice, hepatomegaly, cholestasis, hepatic toxicity, hepatic function abnormal |
| Rare: | hepatic failure, hepatitis cholestatic, hepatosplenomegaly, liver tenderness, asterixis |
| \*\*Skin and subcutaneous tissue disorders\*\* | |
| Common: | rash, pruritis |
| Uncommon: | mouth ulceration, alopecia, dermatitis, erythema, petechiae |
| Rare: | Stevens Johnson syndrome, vesicular rash |
| Not known | Photosensitivity reaction§ |
| \*\*Musculoskeletal and connective tissue disorders\*\* | |
| Uncommon: | back pain, neck pain, musculoskeletal pain, pain in extremity |
| \*\*Renal and urinary disorders\*\* | |
| Uncommon: | acute renal failure, renal failure, blood creatinine increased |
| Rare: | renal tubular acidosis, interstitial nephritis |
| \*\*Reproductive system and breast disorders\*\* | |
| Uncommon: | menstrual disorder |
| Rare: | breast pain |
| \*\*General disorders and administration site conditions\*\* | |
| Common: | pyrexia (fever), asthenia, fatigue |
| Uncommon: | oedema, pain, chills, malaise, chest discomfort, drug intolerance, feeling jittery, mucosal inflammation |
| Rare: | tongue oedema, face oedema |
| \*\*Investigations\*\* | |
| Uncommon: | altered medicine levels, blood phosphorus decreased, chest x-ray abnormal |
\\* Based on adverse reactions observed with the oral suspension, gastro- resistant tablets, concentrate for solution for infusion, and gastro-resistant powder and solvent for oral suspension.
§ See section 4.4.
\*\*Description of selected adverse reactions\*\*
\*Hepatobiliary disorders\*
During post-marketing surveillance of posaconazole oral suspension, severe hepatic injury with fatal outcome has been reported (see section 4.4).
\*\*Reporting of suspected adverse reactions\*\*
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.4.9 Overdose
There is no experience with overdose of posaconazole tablets.
During clinical studies, patients who received posaconazole oral suspension doses up to 1,600 mg/day experienced no different adverse reactions from those reported with patients at the lower doses.
Accidental overdose was noted in one patient who took posaconazole oral suspension 1,200 mg twice a day for 3 days. No adverse reactions were noted by the investigator.
Posaconazole is not removed by haemodialysis. There is no special treatment available in the case of overdose with posaconazole. Supportive care may be considered.
- Instruction Pharmacology
- 5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antimycotics for systemic use, triazole derivatives, ATC code: J02AC04.
\*\*Mechanism of action\*\*
Posaconazole inhibits the enzyme lanosterol 14α-demethylase (CYP51), which catalyses an essential step in ergosterol biosynthesis.
\*\*Microbiology\*\*
Posaconazole has been shown \*in vitro\* to be active against the following microorganisms: \*Aspergillus\* species (\*Aspergillus fumigatus, A. flavus, A. terreus, A. nidulans, A. niger, A. ustus\*)\*, Candida\* species (\*Candida albicans,\* \*C. glabrata, C. krusei, C. parapsilosis, C. tropicalis, C. dubliniensis, C. famata, C. inconspicua, C. lipolytica, C. norvegensis, C. pseudotropicalis\*), \*Coccidioides immitis, Fonsecaea pedrosoi,\* and species of \*Fusarium, Rhizomucor, Mucor\*, and \*Rhizopus\*. The microbiological data suggest that posaconazole is active against \*Rhizomucor, Mucor,\* and \*Rhizopus;\* however, the clinical data are currently too limited to assess the efficacy of posaconazole against these causative agents.
The following \*in vitro\* data are available, but their clinical significance is unknown. In a surveillance study of > 3,000 clinical mold isolates from 2010- 2018, 90 % of non-\*Aspergillus\* fungi exhibited the following \*in vitro\* minimum inhibitory concentration (MIC): \*Mucorales\* spp (n=81) of 2 mg/L; \*Scedosporium apiospermum/S. boydii\* (n=65) of 2 mg/L; \*Exophiala dermatiditis\* (n=15) of 0.5 mg/L, and \*Purpureocillium lilacinum\* (n=21) of 1 mg/L.
\*\*Resistance\*\*
Clinical isolates with decreased susceptibility to posaconazole have been identified. The principle mechanism of resistance is the acquisition of substitutions in the target protein, CYP51.
\*\*Epidemiological Cut-off (ECOFF) Values for\*\* \*\*\*Aspergillus spp\*\*\*\*\*.\*\*
The ECOFF values for posaconazole, which distinguish the wild type population from isolates with acquired resistance, have been determined by EUCAST methodology.
EUCAST ECOFF values:
• \*Aspergillus flavus\*: 0.5 mg/L
• \*Aspergillus fumigatus\*: 0.5 mg/L
• \*Aspergillus nidulans\*: 0.5 mg/L
• \*Aspergillus niger\*: 0.5 mg/L
• \*Aspergillus terreus\*: 0.25 mg/L
There are currently insufficient data to set clinical breakpoints for \*Aspergillus\* spp. ECOFF values do not equate to clinical breakpoints.
\*\*Breakpoints\*\*
EUCAST MIC breakpoints for posaconazole [susceptible (S); resistant (R)]:
• \*Candida albicans\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida tropicalis\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida parapsilosis\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida dubliniensis\*: S ≤0.06 mg/L, R > 0.06 mg/L
There are currently insufficient data to set clinical breakpoints for other \*Candida\* species.
\*\*Combination with other antifungal agents\*\*
The use of combination antifungal therapies should not decrease the efficacy of either posaconazole or the other therapies; however, there is currently no clinical evidence that combination therapy will provide an added benefit.
\*\*Clinical experience\*\*
\*\*\*Summary of posaconazole concentrate for solution for infusion and tablet\*\* \*\*study invasive aspergillosis\*\*\*
The safety and efficacy of posaconazole for the treatment of patients with invasive aspergillosis was evaluated in a double-blind controlled study (study- 69) in 575 patients with proven, probable, or possible invasive fungal infections per EORTC/MSG criteria.
Patients were treated with posaconazole (n=288) concentrate for solution for infusion or tablet given at a dose of 300 mg QD (BID on Day 1). Comparator patients were treated with voriconazole (n=287) given IV at a dose of 6 mg/kg BID Day 1 followed by 4 mg/kg BID, or orally at a dose of 300 mg BID Day 1 followed by 200 mg BID. Median treatment duration was 67 days (posaconazole) and 64 days (voriconazole).
In the intent-to-treat (ITT) population (all subjects who received at least one dose of study drug), 288 patients received posaconazole and 287 patients received voriconazole. The full analysis set population (FAS) is the subset of all subjects within the ITT population who were classified by independent adjudication as having proven or probable invasive aspergillosis: 163 subjects for posaconazole and 171 subjects for voriconazole. The all-cause mortality and global clinical response in these two populations are presented in Table 3 and 4, respectively.
\*\*Table 3.\*\* Posaconazole invasive aspergillosis treatment study 1: all-cause mortality at Day 42 and Day 84, in the ITT and FAS populations
| | | | | | |
| --- | --- | --- | --- | --- | --- |
| | \*\*Posaconazole\*\* | | \*\*Voriconazole\*\* | | |
| Population | N | n (%) | N | n (%) | Difference\\* (95% CI) |
| Mortality in ITT at Day 42 | 288 | 44 (15.3) | 287 | 59 (20.6) | -5.3 % (-11.6, 1.0) |
| Mortality in ITT at Day 84 | 288 | 81 (28.1) | 287 | 88 (30.7) | -2.5 % (-9.9, 4.9) |
| Mortality in FAS at Day 42 | 163 | 31 (19.0) | 171 | 32 (18.7) | 0.3% (-8.2, 8.8) |
| Mortality in FAS at Day 84 | 163 | 56 (34.4) | 171 | 53 (31.0) | 3.1% (-6.9, 13.1) |
| \\* Adjusted treatment difference based on Miettinen and Nurminen's method stratified by randomisation factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme. | | | | | |
\*\*Table 4.\*\* Posaconazole invasive aspergillosis treatment study 1: global clinical response at Week 6 and Week 12 in the FAS population
| | | | | | |
| --- | --- | --- | --- | --- | --- |
| | \*\*Posaconazole\*\* | | \*\*Voriconazole\*\* | | |
| Population | N | Success (%) | N | Success (%) | Difference\\* (95 %CI) |
| Global clinical response in the FAS at 6 weeks | 163 | 73 (44.8) | 171 | 78 (45.6) | -0.6 % (-11.2, 10.1) |
| Global clinical response in the FAS at 12 weeks | 163 | 69 (42.3) | 171 | 79 (46.2) | -3.4 % (-13.9, 7.1) |
| \\* Successful Global Clinical Response was defined as survival with a partial or complete response Adjusted treatment difference based on Miettinen and Nurminen's method stratified by randomisation factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme. | | | | | |
\*\*\*Summary of posaconazole tablet bridging study\*\*\*
Study 5615 was a non-comparative multi-centre study performed to evaluate the pharmacokinetic properties, safety, and tolerability of posaconazole tablet. Study 5615 was conducted in a similar patient population to that previously studied in the pivotal posaconazole oral suspension clinical program. The pharmacokinetics and safety data from Study 5615 were bridged to the existing data (including efficacy data) with the oral suspension.
The subject population included: 1) patients with AML or MDS who had recently received chemotherapy and had developed or were anticipated to develop significant neutropenia, or 2) patients who had undergone a HSCT and were receiving immunosuppressive therapy for prevention or treatment of GVHD. Two different dosing groups were evaluated: 200 mg twice daily on Day 1, followed by 200 mg once daily thereafter (Part IA) and 300 mg twice daily on Day 1, followed by 300 mg once daily thereafter (Part 1B and Part 2).
Serial PK samples were collected on Day 1 and at steady-state on Day 8 for all Part 1 subjects and a subset of Part 2 subjects. Moreover, sparse PK samples were collected at several days during steady state before the next dose (Cmin) for a larger subject population. Based on average Cmin concentrations, a predicted average concentration (Cav) could be calculated for 186 subjects dosed with 300 mg. PK analysis in patients of Cav found that 81 % of the subjects treated with the 300 mg once daily dose attained steady state predicted Cav between 500-2,500 ng/mL. One subject (<1 %) had a predicted Cav below 500 ng/mL and 19 % of the subjects had a predicted Cav above 2,500 ng/mL. Subjects achieved a mean predicted Cav at steady state of 1,970 ng/mL.
In Table 5 a comparison is shown of exposure (Cav) after administration of posaconazole tablet and posaconazole oral suspension at therapeutic doses in patients depicted as quartile analysis. Exposures after tablet administration are generally higher than, but overlapping with, exposures after administration of posaconazole oral suspension.
\*\*Table 5.\*\* Cav quartile analyses of pivotal patient studies with posaconazole tablet and oral suspension
| | | | | |
| --- | --- | --- | --- | --- |
| | \*\*Posaconazole tablet\*\* | \*\*Posaconazole oral suspension\*\* | | |
| \*\*Prophylaxis in AML and HSCT Study 5615\*\* | \*\*Prophylaxis in GVHD Study 316\*\* | \*\*Prophylaxis in Neutropenia Study 1899\*\* | \*\*Treatment - Invasive Aspergillosis Study 0041\*\* |
| \*\*300 mg once daily (Day 1 300 mg twice daily)\\*\*\* | \*\*200 mg three times daily\*\* | \*\*200 mg three times daily\*\* | \*\*200 mg four times daily (hospitalized) then 400 mg twice daily\*\* |
| \*\*Quartile\*\* | \*\*pCav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* |
| Q1 | 442 – 1,223 | 22 – 557 | 90 – 322 | 55 – 277 |
| Q2 | 1,240 – 1,710 | 557 – 915 | 322 – 490 | 290 – 544 |
| Q3 | 1,719 – 2,291 | 915 – 1,563 | 490 – 734 | 550 – 861 |
| Q4 | 2,304 – 9,523 | 1,563 – 3,650 | 734 – 2,200 | 877 – 2,010 |
| pCav: predicted Cav Cav = the average concentration when measured at steady state \\*20 patients received 200 mg once daily (Day 1 200 mg twice daily) | | | | |
\*\*\*Summary of posaconazole oral suspension studies\*\*\*
\*Invasive aspergillosis\*
Oral posaconazole suspension 800 mg/day in divided doses was evaluated for the treatment of invasive aspergillosis in patients with disease refractory to amphotericin B (including liposomal formulations) or itraconazole or in patients who were intolerant of these medicinal products in a non-comparative salvage therapy study (Study 0041). Clinical outcomes were compared with those in an external control group derived from a retrospective review of medical records. The external control group included 86 patients treated with available therapy (as above) mostly at the same time and at the same sites as the patients treated with posaconazole. Most of the cases of aspergillosis were considered to be refractory to prior therapy in both the posaconazole group (88%) and in the external control group (79 %).
As shown in Table 6, a successful response (complete or partial resolution) at the end of treatment was seen in 42 % of posaconazole-treated patients compared to 26 % of the external group. However, this was not a prospective, randomised controlled study and so all comparisons with the external control group should be viewed with caution.
\*\*Table 6.\*\* Overall efficacy of posaconazole oral suspension at the end of treatment for invasive aspergillosis in comparison to an external control group
| | | | | |
| --- | --- | --- | --- | --- |
| | \*\*Posaconazole oral suspension\*\* | | \*\*External control group\*\* | |
| Overall Response | 45/107 (42 %) | | 22/86 (26 %) | |
| \*\*Success by Species\*\* All mycologically confirmed \*Aspergillus spp.2\* | 34/76 | (45 %) | 19/74 | (26 %) |
| \*A. fumigatus\* | 12/29 | (41 %) | 12/34 | (35 %) |
| \*A. flavus\* | 10/19 | (53 %) | 3/16 | (19 %) |
| \*A. terreus\* | 4/14 | (29 %) | 2/13 | (15 %) |
| \*A. niger\* | 3/5 | (60 %) | 2/7 | (29 %) |
2 Includes other less common species or species unknown
\*Fusarium spp.\*
11 of 24 patients who had proven or probable fusariosis were successfully treated with posaconazole oral suspension 800 mg/day in divided doses for a median of 124 days and up to 212 days. Among eighteen patients who were intolerant or had infections refractory to amphotericin B or itraconazole, seven patients were classed as responders.
\*Chromoblastomycosis/Mycetoma\*
9 of 11 patients were successfully treated with posaconazole oral suspension 800 mg/day in divided doses for a median of 268 days and up to 377 days. Five of these patients had chromoblastomycosis due to \*Fonsecaea pedrosoi\* and 4 had mycetoma, mostly due to \*Madurella\* species.
\*Coccidioidomycosis\*
11 of 16 patients were successfully treated (at the end of treatment complete or partial resolution of signs and symptoms present at baseline) with posaconazole oral suspension 800 mg/day in divided doses for a median of 296 days and up to 460 days.
\*Prophylaxis of Invasive Fungal Infections (IFIs) (Studies 316 and 1899)\*
Two randomised, controlled prophylaxis studies were conducted among patients at high-risk for developing invasive fungal infections.
Study 316 was a randomised, double-blind study of posaconazole oral suspension (200 mg three times a day) versus fluconazole capsules (400 mg once daily) in allogeneic hematopoietic stem cell transplant recipients with graft-versus-host disease (GVHD). The primary efficacy endpoint was the incidence of proven/probable IFIs at 16 weeks post-randomisation as determined by an independent, blinded external expert panel. A key secondary endpoint was the incidence of proven/probable IFIs during the on-treatment period (first dose to last dose of study medicinal product + 7 days). The majority (377/600, [63 %]) of patients included had Acute Grade 2 or 3 or chronic extensive (195/600, [32.5 %]) GVHD at study start. The mean duration of therapy was 80 days for posaconazole and 77 days for fluconazole.
Study 1899 was a randomised, evaluator-blinded study of posaconazole oral suspension (200 mg three times a day) versus fluconazole suspension (400 mg once daily) or itraconazole oral solution (200 mg twice a day) in neutropenic patients who were receiving cytotoxic chemotherapy for acute myelogenous leukaemia or myelodysplastic syndromes. The primary efficacy endpoint was the incidence of proven/probable IFIs as determined by an independent, blinded external expert panel during the on-treatment period. A key secondary endpoint was the incidence of proven/probable IFIs at 100 days post- randomisation. New diagnosis of acute myelogenous leukaemia was the most common underlying condition (435/602, [72 %]). The mean duration of therapy was 29 days for posaconazole and 25 days for fluconazole/itraconazole.
In both prophylaxis studies, aspergillosis was the most common breakthrough infection. See Table 7 and 8 for results from both studies. There were fewer breakthrough \*Aspergillus\* infections in patients receiving posaconazole prophylaxis when compared to control patients.
\*\*Table 7.\*\* Results from clinical studies in prophylaxis of Invasive Fungal Infections
| | | | |
| --- | --- | --- | --- |
| \*\*Study\*\* | \*\*Posaconazole oral suspension\*\* | \*\*Controla\*\* | \*\*P-Value\*\* |
| \*\*Proportion (%) of patients with proven/probable IFIs\*\* | | | |
| \*\*On-treatment periodb\*\* | | | |
| 1899d | 7/304 (2) | 25/298 (8) | 0.0009 |
| 316e | 7/291 (2) | 22/288 (8) | 0.0038 |
| \*\*Fixed-time periodc\*\* | | | |
| 1899d | 14/304 (5) | 33/298 (11) | 0.0031 |
| 316d | 16/301 (5) | 27/299 (9) | 0.0740 |
FLU = fluconazole; ITZ = itraconazole; POS = posaconazole.
a: FLU/ITZ (1899); FLU (316).
b: In 1899 this was the period from randomisation to last dose of study medicinal product plus 7 days; in 316 it was the period from first dose to last dose of study medicinal product plus 7 days.
c: In 1899, this was the period from randomisation to 100 days post- randomisation; in 316 it was the period from the baseline day to 111 days post-baseline.
d: All randomised
e: All treated
\*\*Table 8.\*\* Results from clinical studies in prophylaxis of Invasive Fungal Infections
| | | |
| --- | --- | --- |
| \*\*Study\*\* | \*\*Posaconazole oral suspension\*\* | \*\*Controla\*\* |
| \*\*Proportion (%) of patients with proven/probable Aspergillosis\*\* | | |
| \*\*On-treatment periodb\*\* | | |
| 1899d | 2/304 (1) | 20/298 (7) |
| 316e | 3/291 (1) | 17/288 (6) |
| \*\*Fixed-time periodc\*\* | | |
| 1899d | 4/304 (1) | 26/298 (9) |
| 316d | 7/301 (2) | 21/299 (7) |
FLU = fluconazole; ITZ = itraconazole; POS = posaconazole.
a: FLU/ITZ (1899); FLU (316).
b: In 1899 this was the period from randomisation to last dose of study medicinal product plus 7 days; in 316 it was the period from first dose to last dose of study medicinal product plus 7 days.
c: In 1899, this was the period from randomisation to 100 days post- randomisation; in 316 it was the period from the baseline day to 111 days post-baseline.
d: All randomised
e: All treated
In Study 1899, a significant decrease in all cause mortality in favour of posaconazole was observed [POS 49/304 (16 %) vs. FLU/ITZ 67/298 (22 %) p= 0.048]. Based on Kaplan-Meier estimates, the probability of survival up to day 100 after randomisation, was significantly higher for posaconazole recipients; this survival benefit was demonstrated when the analysis considered all causes of death (P= 0.0354) as well as IFI-related deaths (P = 0.0209).
In Study 316, overall mortality was similar (POS, 25 %; FLU, 28 %); however, the proportion of IFI-related deaths was significantly lower in the POS group (4/301) compared with the FLU group (12/299; P= 0.0413).
\*\*Paediatric population\*\*
There is limited paediatric experience for posaconazole tablets.
Three patients 14-17 years of age were treated with posaconazole concentrate for solution for infusion and tablet 300 mg/day (BID on Day 1 followed by QD thereafter) in the study of treatment of invasive aspergillosis.
The safety and efficacy of posaconazole (posaconazole gastro-resistant powder and solvent for oral suspension; posaconazole concentrate for solution for infusion) have been established in paediatric patients 2 to less than 18 years of age. Use of posaconazole in these age groups is supported by evidence from adequate and well-controlled studies of posaconazole in adults and pharmacokinetic and safety data from paediatric studies (see section 5.2). No new safety signals associated with the use of posaconazole in paediatric patients were identified in the paediatric studies (see section 4.8).
Safety and efficacy in paediatric patients below the age of 2 years have not been established.
No data are available.
\*\*Electrocardiogram evaluation\*\*
Multiple, time-matched ECGs collected over a 12 hour period were obtained before and during administration of posaconazole oral suspension (400 mg twice daily with high fat meals) from 173 healthy male and female volunteers aged 18 to 85 years. No clinically relevant changes in the mean QTc (Fridericia) interval from baseline were observed.5.2 Pharmacokinetic properties
\*\*Pharmacokinetic / Pharmacodynamic relationships\*\*
A correlation between total medicinal product exposure divided by MIC (AUC/MIC) and clinical outcome was observed. The critical ratio for subjects with \*Aspergillus\* infections was ~200. It is particularly important to try to ensure that maximal plasma levels are achieved in patients infected with \*Aspergillus\* (see sections 4.2 and 5.2 on recommended dose regimens).
\*\*Absorption\*\*
Posaconazole tablets are absorbed with a median Tmax of 4 to 5 hours and exhibits dose proportional pharmacokinetics after single and multiple dosing up to 300 mg.
Following a single dose administration of 300 mg posaconazole Amarox tablets after a high fat meal to healthy volunteers, the AUC0-72 hours and Cmax were higher compared to administration under fasted condition (51 % and 16% for AUC0-72 hours and Cmax respectively). Based on a population pharmacokinetic model, posaconazole Cav is increased 20 % when given with a meal compared to a fasted state.
Posaconazole plasma concentrations following administration of posaconazole tablets may increase over time in some patients. The reason for this time- dependency is not completely understood.
\*\*Distribution\*\*
Posaconazole, after administration of the tablet, has a mean apparent volume of distribution of 394 L (42 %), ranging between 294-583 L among the studies in healthy volunteers.
Posaconazole is highly protein bound (> 98 %), predominantly to serum albumin.
\*\*Biotransformation\*\*
Posaconazole does not have any major circulating metabolites and its concentrations are unlikely to be altered by inhibitors of CYP450 enzymes. Of the circulating metabolites, the majority are glucuronide conjugates of posaconazole with only minor amounts of oxidative (CYP450 mediated) metabolites observed. The excreted metabolites in urine and faeces account for approximately 17 % of the administered radiolabelled dose.
\*\*Elimination\*\*
Posaconazole after administration of the tablets, is slowly eliminated with a mean half-life (t½) of 29 hours (range 26 to 31 hours) and a mean apparent clearance ranging from 7.5 to 11 L/hr. After administration of 14C- posaconazole, radioactivity was predominantly recovered in the faeces (77 % of the radiolabelled dose) with the major component being parent compound (66 % of the radiolabelled dose). Renal clearance is a minor elimination pathway, with 14 % of the radiolabelled dose excreted in urine (< 0.2 % of the radiolabelled dose is parent compound). Steady-state plasma concentrations are attained by Day 6 at the 300 mg dose (once daily after twice daily loading dose at Day 1).
\*\*Pharmacokinetics in special populations\*\*
Based on a population pharmacokinetic model evaluating posaconazole pharmacokinetics, steady state posaconazole concentrations were predicted in patients administered posaconazole concentrate for solution for infusion or tablets 300 mg once a day following BID dosing on Day 1 for the treatment of invasive aspergillosis and prophylaxis of invasive fungal infections.
\*\*Table 9.\*\* Population predicted median (10th percentile, 90th percentile) posaconazole steady state plasma concentrations in patients following administration of posaconazole concentrate for solution for infusion or tablets 300 mg QD (BID on Day 1)
| | | | |
| --- | --- | --- | --- |
| \*\*Regimen\*\* | \*\*Population\*\* | \*\*Cav (ng/mL)\*\* | \*\*Cmin (ng/mL)\*\* |
| Tablet-(Fasted) | Prophylaxis | 1,550 (874; 2,690) | 1,330 (667; 2,400) |
| Treatment of Invasive Aspergillosis | 1,490 (663; 3,230) | 1,780 (879; 3,540) |
| Concentrate for Solution for Infusion | Prophylaxis | 1,890 (1,100; 3,150) | 1,500 (745; 2,660) |
| Treatment of Invasive Aspergillosis | 2,240 (1,230; 4,160) | 1,780 (874; 3,620) |
The population pharmacokinetic analysis of posaconazole in patients suggests that race, sex, renal impairment and disease (prophylaxis or treatment) have no clinically meaningful effect on the pharmacokinetics of posaconazole.
\*Children (< 18 years)\*
There is limited (n=3) paediatric experience with posaconazole tablets.
The pharmacokinetics of posaconazole oral suspension have been evaluated in paediatric patients.
Following administration of 800 mg per day of posaconazole oral suspension as a divided dose for treatment of invasive fungal infections, mean trough plasma concentrations from 12 patients 8 - 17 years of age (776 ng/mL) were similar to concentrations from 194 patients 18 - 64 years of age (817 ng/mL). No pharmacokinetic data are available from paediatric patients less than 8 years of age.
Similarly, in the prophylaxis studies, the mean steady-state posaconazole average concentration (Cav) was comparable among ten adolescents (13-17 years of age) to Cav achieved in adults (≥ 18 years of age).
\*Gender\*
The pharmacokinetics of posaconazole tablets are comparable in men and women.
\*Elderly\*
No overall differences in safety were observed between the geriatric patients and younger patients.
The population pharmacokinetic model of posaconazole concentrate for solution for infusion and tablets indicates that posaconazole clearance is related to age. Posaconazole Cav is generally comparable between young and elderly patients (≥ 65 years of age); however, the Cav is increased by 11 % in the very elderly (≥ 80 years). It is, therefore, suggested to closely monitor very elderly patients (≥ 80 years) for adverse events.
The pharmacokinetics of posaconazole tablets are comparable in young and elderly subjects (≥ 65 years of age).
Pharmacokinetic differences based upon age are not considered to be clinically relevant; therefore, no dose adjustment is required.
\*Race\*
There is insufficient data among different races with posaconazole tablets.
There was a slight decrease (16 %) in the AUC and Cmax of posaconazole oral suspension in Black subjects relative to Caucasian subjects. However, the safety profile of posaconazole between the Black and Caucasian subjects was similar.
\*Weight\*
The population pharmacokinetic model of posaconazole concentrate for solution for infusion and tablets indicates that posaconazole clearance is related to weight. In patients > 120 kg, the Cav is decreased by 25 % and in patients <50 kg, the Cav is increased by 19 %. It is, therefore, suggested to closely monitor for breakthrough fungal infections in patients weighing more than 120 kg.
\*Renal impairment\*
Following single-dose administration of posaconazole oral suspension, there was no effect of mild and moderate renal impairment (n=18, Cl cr ≥ 20 mL/min/1.73 m2) on posaconazole pharmacokinetics; therefore, no dose adjustment is required. In subjects with severe renal impairment (n=6, Cl cr < 20 mL/min/1.73 m2), the AUC of posaconazole was highly variable [> 96 % CV (coefficient of variance)] compared to other renal groups [< 40 % CV]. However, as posaconazole is not significantly renally eliminated, an effect of severe renal impairment on the pharmacokinetics of posaconazole is not expected and no dose adjustment is recommended. Posaconazole is not removed by haemodialysis.
Similar recommendations apply to posaconazole tablets; however, a specific study has not been conducted with the posaconazole tablets.
\*Hepatic impairment\*
After a single oral dose of 400 mg posaconazole oral suspension to patients with mild (Child-Pugh Class A), moderate (Child-Pugh Class B) or severe (Child-Pugh Class C) hepatic impairment (six per group), the mean AUC was 1.3 to 1.6-fold higher compared to that for matched control subjects with normal hepatic function. Unbound concentrations were not determined and it cannot be excluded that there is a larger increase in unbound posaconazole exposure than the observed 60 % increase in total AUC. The elimination half- life (t1/2) was prolonged from approximately 27 hours up to ~43 hours in respective groups. No dose adjustment is recommended for patients with mild to severe hepatic impairment but caution is advised due to the potential for higher plasma exposure.
Similar recommendations apply to posaconazole tablets; however, a specific study has not been conducted with the posaconazole tablets.5.3 Preclinical safety data
As observed with other azole antifungal agents, effects related to inhibition of steroid hormone synthesis were seen in repeated-dose toxicity studies with posaconazole. Adrenal suppressive effects were observed in toxicity studies in rats and dogs at exposures equal to or greater than those obtained at therapeutic doses in humans.
Neuronal phospholipidosis occurred in dogs dosed for ≥ 3 months at lower systemic exposures than those obtained at therapeutic doses in humans. This finding was not seen in monkeys dosed for one year. In twelve-month neurotoxicity studies in dogs and monkeys, no functional effects were observed on the central or peripheral nervous systems at systemic exposures greater than those achieved therapeutically.
Pulmonary phospholipidosis resulting in dilatation and obstruction of the alveoli was observed in the 2-year study in rats. These findings are not necessarily indicative of a potential for functional changes in humans.
No effects on electrocardiograms, including QT and QTc intervals, were seen in a repeat dose safety pharmacology study in monkeys at maximal plasma concentrations 8.5-fold greater than the concentrations obtained at therapeutic doses in humans. Echocardiography revealed no indication of cardiac decompensation in a repeat dose safety pharmacology study in rats at a systemic exposure 2.1-fold greater than that achieved therapeutically. Increased systolic and arterial blood pressures (up to 29 mm-Hg) were seen in rats and monkeys at systemic exposures 2.1-fold and 8.5-fold greater, respectively, than those achieved with the human therapeutic doses.
Reproduction, peri- and postnatal development studies were conducted in rats. At exposures lower than those obtained at therapeutic doses in humans, posaconazole caused skeletal variations and malformations, dystocia, increased length of gestation, reduced mean litter size and postnatal viability. In rabbits, posaconazole was embryotoxic at exposures greater than those obtained at therapeutic doses. As observed with other azole antifungal agents, these effects on reproduction were considered to be due to a treatment-related effect on steroidogenesis.
Posaconazole was not genotoxic in \*in vitro\* and \*in vivo\* studies. Carcinogenicity studies did not reveal special hazards for humans.
In a nonclinical study using intravenous administration of posaconazole in very young dogs (dosed from 2-8 weeks of age) an increase in the incidence of brain ventricle enlargement was observed in treated animals as compared with concurrent control animals. No difference in the incidence of brain ventricle enlargement between control and treated animals was observed following the subsequent 5 month treatment-free period. There were no neurologic, behavioural or developmental abnormalities in the dogs with this finding, and a similar brain finding was not seen with either oral posaconazole administration to juvenile dogs (4 days to 9 months of age) or intravenous posaconazole administration to juvenile dogs (10 weeks to 23 weeks of age). The clinical significance of this finding is unknown.
- Instruction Pharmaceutical Particulars
- 6.1 List of excipients
\*\*Tablet core:\*\*
Hypromellose acetate succinate
Cellulose, microcrystalline
Hydroxypropylcellulose
Croscarmellose sodium
Silica, colloidal anhydrous
Magnesium stearate
\*\*Film coating:\*\*
Polyvinyl alcohol-part. hydrolyzed (E1203)
Titanium dioxide (E171)
Macrogol (E1521)
Talc (E553b)
Iron oxide yellow (E172)
Iron oxide red (E172)6.2 Incompatibilities
Not applicable.6.3 Shelf life
3 years6.4 Special precautions for storage
This medicinal product does not require any special storage conditions6.5 Nature and contents of container
White Opaque PVC/Aclar-Alu blister pack of 24 and 96 tablets.
Not all pack sizes may be marketed.6.6 Special precautions for disposal and other handling
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
- Instruction Content
- ## Composition
Each gastro-resistant tablet contains 100 mg of posaconazole.
For the full list of excipients, see section 6.1.
## Pharmaceutical Form
Gastro-resistant tablet.
Light orange, oblong shaped, film-coated tablets with approx. dimensions of 17.50 mm X 6.80 mm de-bossed with "H" on one side and "P11" on the other side.
## Clinical Particulars
4.1 Therapeutic indications
Posaconazole Amarox gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4.2 and 5.1):
- Invasive aspergillosis
Posaconazole Amarox gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4.2 and 5.1):
- Invasive aspergillosis in patients with disease that is refractory to amphotericin B or itraconazole or in patients who are intolerant of these medicinal products;
- Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B;
- Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;
- Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products.
Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy.
Posaconazole Amarox gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4.2 and 5.1):
- Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high-risk of developing invasive fungal infections;
- Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high- dose immunosuppressive therapy for graft versus host disease and who are at high-risk of developing invasive fungal infections.
Please refer to the Summary of Product Characteristics of posaconazole oral suspension for use in oropharyngeal candidiasis.4.2 Posology and method of administration
Treatment should be initiated by a physician experienced in the management of fungal infections or in the supportive care of high-risk patients for which posaconazole is indicated as prophylaxis.
\*\*Non-interchangeability between posaconazole Amarox tablets and posaconazole oral suspension\*\*
The tablet is not to be used interchangeably with the oral suspension due to the differences between these two formulations in frequency of dosing, administration with food and plasma drug concentration achieved. Therefore, follow the specific dose recommendations for each formulation.
\*\*Posology\*\*
Posaconazole is also available as 40 mg/mL oral suspension, 300 mg concentrate for solution for infusion and 300 mg gastro-resistant powder and solvent for oral suspension. Posaconazole tablets generally provide higher plasma drug exposures than posaconazole oral suspension under both fed and fasted conditions. Therefore, the tablets are the preferred formulation to optimise plasma concentrations.
Recommended dose in paediatric patients from 2 years of age weighing more than 40 kg and in adults is shown in Table 1.
Posaconazole Amarox gastro-resistant powder and solvent for oral suspension is recommended for oral use in paediatric patients 2 years of age and older weighing 40 kg or less. Refer to the gastro-resistant powder and solvent for oral suspension SmPC for additional dosing information.
\*\*Table 1.\*\* Recommended dose in paediatric patients from 2 years of age weighing more than 40 kg and in adults according to indication
| | |
| --- | --- |
| \*\*Indication\*\* | \*\*Dose and duration of therapy\*\* (See section 5.2) |
| Treatment of invasive aspergillosis (only for adults) | Loading dose of 300 mg (three 100 mg tablets or 300 mg concentrate for solution for infusion) twice a day on the first day, then 300 mg (three 100 mg tablets or 300 mg concentrate for solution for infusion) once a day thereafter. Each tablet dose may be taken without regard to food intake. Recommended total duration of therapy is 6-12 weeks. Switching between intravenous and oral administration is appropriate when clinically indicated. |
| Refractory invasive fungal infections (IFI)/patients with IFI intolerant to 1st line therapy | Loading dose of 300 mg (three 100 mg tablets) twice a day on the first day, then 300 mg (three 100 mg tablets) once a day thereafter. Each dose may be taken without regard to food intake. Duration of therapy should be based on the severity of the underlying disease, recovery from immunosuppression, and clinical response. |
| Prophylaxis of invasive fungal infections | Loading dose of 300 mg (three 100 mg tablets) twice a day on the first day, then 300 mg (three 100 mg tablets) once a day thereafter. Each dose may be taken without regard to food intake. Duration of therapy is based on recovery from neutropenia or immunosuppression. For patients with acute myelogenous leukaemia or myelodysplastic syndromes, prophylaxis with posaconazole should start several days before the anticipated onset of neutropenia and continue for 7 days after the neutrophil count rises above 500 cells per mm3. |
\*\*Special populations\*\*
\*Renal impairment\*
An effect of renal impairment on the pharmacokinetics of posaconazole is not expected and no dose adjustment is recommended (see section 5.2).
\*Hepatic impairment\*
Limited data on the effect of hepatic impairment (including Child-Pugh C classification of chronic liver disease) on the pharmacokinetics of posaconazole demonstrate an increase in plasma exposure compared to subjects with normal hepatic function, but do not suggest that dose adjustment is necessary (see sections 4.4 and 5.2). It is recommended to exercise caution due to the potential for higher plasma exposure.
\*Paediatric population\*
The safety and efficacy of posaconazole in children aged below 2 years have not been established.
No clinical data are available.
\*\*Method of administration\*\*
For oral use
Posaconazole Amarox gastro-resistant tablets may be taken with or without food (see section 5.2). The tablets should be swallowed whole with water and should not be crushed, chewed, or broken.4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Co-administration with ergot alkaloids (see section 4.5).
Co-administration with the CYP3A4 substrates terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine since this may result in increased plasma concentrations of these medicinal products, leading to QTc prolongation and rare occurrences of torsades de pointes (see sections 4.4 and 4.5).
Co-administration with the HMG-CoA reductase inhibitors simvastatin, lovastatin and atorvastatin (see section 4.5).
Co-administration during the initiation and dose-titration phase of venetoclax in Chronic Lymphocytic Leukaemia (CLL) patients (see sections 4.4 and 4.5).4.4 Special warnings and precautions for use
\*\*Hypersensitivity\*\*
There is no information regarding cross-sensitivity between posaconazole and other azole antifungal agents. Caution should be used when prescribing posaconazole to patients with hypersensitivity to other azoles.
\*\*Hepatic toxicity\*\*
Hepatic reactions (e.g. mild to moderate elevations in ALT, AST, alkaline phosphatase, total bilirubin and/or clinical hepatitis) have been reported during treatment with posaconazole. Elevated liver function tests were generally reversible on discontinuation of therapy and in some instances these tests normalised without interruption of therapy. Rarely, more severe hepatic reactions with fatal outcomes have been reported.
Posaconazole should be used with caution in patients with hepatic impairment due to limited clinical experience and the possibility that posaconazole plasma levels may be higher in these patients (see sections 4.2 and 5.2).
\*\*Monitoring of hepatic function\*\*
Liver function tests should be evaluated at the start of and during the course of posaconazole therapy. Patients who develop abnormal liver function tests during posaconazole therapy must be routinely monitored for the development of more severe hepatic injury. Patient management should include laboratory evaluation of hepatic function (particularly liver function tests and bilirubin).
Discontinuation of posaconazole should be considered if clinical signs and symptoms are consistent with development of liver disease.
\*\*QTc prolongation\*\*
Some azoles have been associated with prolongation of the QTc interval. Posaconazole must not be administered with medicinal products that are substrates for CYP3A4 and are known to prolong the QTc interval (see sections 4.3 and 4.5). Posaconazole should be administered with caution to patients with pro-arrhythmic conditions such as:
• Congenital or acquired QTc prolongation
• Cardiomyopathy, especially in the presence of cardiac failure
• Sinus bradycardia
• Existing symptomatic arrhythmias
• Concomitant use with medicinal products known to prolong the QTc interval (other than those mentioned in section 4.3).
Electrolyte disturbances, especially those involving potassium, magnesium or calcium levels, should be monitored and corrected as necessary before and during posaconazole therapy.
\*\*Drug interactions\*\*
Posaconazole is an inhibitor of CYP3A4 and should only be used under specific circumstances during treatment with other medicinal products that are metabolised by CYP3A4 (see section 4.5).
\*\*Midazolam and other benzodiazepines\*\*
Due to the risk of prolonged sedation and possible respiratory depression co- administration of posaconazole with any benzodiazepines metabolised by CYP3A4 (e.g. midazolam, triazolam, alprazolam) should only be considered if clearly necessary. Dose adjustment of benzodiazepines metabolised by CYP3A4 should be considered (see section 4.5).
\*\*Vincristine toxicity\*\*
Concomitant administration of azole antifungals, including posaconazole, with vincristine has been associated with neurotoxicity and other serious adverse reactions, including seizures, peripheral neuropathy, syndrome of inappropriate antidiuretic hormone secretion, and paralytic ileus. Reserve azole antifungals, including posaconazole, for patients receiving a vinca alkaloid, including vincristine, who have no alternative antifungal treatment options (see section 4.5).
\*\*Venetoclax toxicity\*\*
Concomitant administration of strong CYP3A inhibitors, including posaconazole, with the CYP3A4 substrate venetoclax, may increase venetoclax toxicities, including the risk of tumour lysis syndrome (TLS) and neutropenia (see sections 4.3 and 4.5). Refer to the venetoclax SmPC for detailed guidance.
\*\*Rifamycin antibacterials (rifampicin, rifabutin), flucloxacillin, certain anticonvulsants (phenytoin, carbamazepine, phenobarbital, primidone), and efavirenz.\*\*
Posaconazole concentrations may be significantly lowered in combination; therefore, concomitant use with posaconazole should be avoided unless the benefit to the patient outweighs the risk (see section 4.5).
\*\*Plasma exposure\*\*
Posaconazole plasma concentrations following administration of posaconazole tablets are generally higher than those obtained with posaconazole oral suspension. Posaconazole plasma concentrations following administration of posaconazole tablets may increase over time in some patients (see section 5.2).
\*\*Gastrointestinal dysfunction\*\*
There are limited pharmacokinetic data in patients with severe gastrointestinal dysfunction (such as severe diarrhoea). Patients who have severe diarrhoea or vomiting should be monitored closely for breakthrough fungal infections.
\*\*Photosensitivity reaction\*\*
Posaconazole may cause increased risk of photosensitivity reaction. Patients should be advised to avoid sun exposure during treatment without adequate protection such as protective clothing and sunscreen with a high sun protection factor (SPF).
\*\*Sodium\*\*
This medicinal product contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially 'sodium-free'.4.5 Interaction with other medicinal products and other forms of interaction
\*\*Effects of other medicinal products on posaconazole\*\*
Posaconazole is metabolised via UDP glucuronidation (phase 2 enzymes) and is a substrate for p-glycoprotein (P-gp) efflux \*in vitro\*. Therefore, inhibitors (e.g. verapamil, ciclosporin, quinidine, clarithromycin, erythromycin, etc.) or inducers (e.g. rifampicin, rifabutin, certain anticonvulsants, etc.) of these clearance pathways may increase or decrease posaconazole plasma concentrations, respectively.
\*Rifabutin\*
Rifabutin (300 mg once a day) decreased the Cmax (maximum plasma concentration) and AUC (area under the plasma concentration time curve) of posaconazole to 57 % and 51 %, respectively. Concomitant use of posaconazole and rifabutin and similar inducers (e.g. rifampicin) should be avoided unless the benefit to the patient outweighs the risk. See also below regarding the effect of posaconazole on rifabutin plasma levels.
\*\*Flucloxacillin\*\*
Flucloxacillin (a CYP450 inducer) may decrease plasma posaconazole concentrations. Concomitant use of posaconazole and flucloxacillin should be avoided unless the benefit to the patient outweighs the risk (see section 4.4).
\*Efavirenz\*
Efavirenz (400 mg once a day) decreased the Cmax and AUC of posaconazole by 45 % and 50 %, respectively. Concomitant use of posaconazole and efavirenz should be avoided unless the benefit to the patient outweighs the risk.
\*Fosamprenavir\*
Combining fosamprenavir with posaconazole may lead to decreased posaconazole plasma concentrations. If concomitant administration is required, close monitoring for breakthrough fungal infections is recommended. Repeat dose administration of fosamprenavir (700 mg twice daily x 10 days) decreased the Cmax and AUC of posaconazole oral suspension (200 mg once daily on the 1st day, 200 mg twice daily on the 2nd day, then 400 mg twice daily x 8 Days) by 21 % and 23 %, respectively. The effect of posaconazole on fosamprenavir levels when fosamprenavir is given with ritonavir is unknown.
\*Phenytoin\*
Phenytoin (200 mg once a day) decreased the Cmax and AUC of posaconazole by 41 % and 50 %, respectively. Concomitant use of posaconazole and phenytoin and similar inducers (e.g. carbamazepine, phenobarbital, primidone) should be avoided unless the benefit to the patient outweighs the risk.
\*H2 receptor antagonists and proton pump inhibitors\*
No clinically relevant effects were observed when posaconazole tablets are concomitantly used with antacids, H2-receptor antagonists and proton pump inhibitors. No dose adjustment of posaconazole tablets is required when posaconazole tablets are concomitantly used with antacids, H2-receptor antagonists and proton pump inhibitors.
\*\*Effects of posaconazole on other medicinal products\*\*
Posaconazole is a potent inhibitor of CYP3A4. Co-administration of posaconazole with CYP3A4 substrates may result in large increases in exposure to CYP3A4 substrates as exemplified by the effects on tacrolimus, sirolimus, atazanavir and midazolam below. Caution is advised during co- administration of posaconazole with CYP3A4 substrates administered intravenously and the dose of the CYP3A4 substrate may need to be reduced. If posaconazole is used concomitantly with CYP3A4 substrates that are administered orally, and for which an increase in plasma concentrations may be associated with unacceptable adverse reactions, plasma concentrations of the CYP3A4 substrate and/or adverse reactions should be closely monitored and the dose adjusted as needed. Several of the interaction studies were conducted in healthy volunteers in whom a higher exposure to posaconazole occurs compared to patients administered the same dose. The effect of posaconazole on CYP3A4 substrates in patients might be somewhat lower than that observed in healthy volunteers, and is expected to be variable between patients due to the variable posaconazole exposure in patients. The effect of co-administration with posaconazole on plasma levels of CYP3A4 substrates may also be variable within a patient.
\*Terfenadine, astemizole, cisapride, pimozide, halofantrine and quinidine (CYP3A4 substrates)\*
Co-administration of posaconazole and terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine is contraindicated. Co-administration may result in increased plasma concentrations of these medicinal products, leading to QTc prolongation and rare occurrences of torsades de pointes (see section 4.3).
\*Ergot alkaloids\*
Posaconazole may increase the plasma concentration of ergot alkaloids (ergotamine and dihydroergotamine), which may lead to ergotism. Co- administration of posaconazole and ergot alkaloids is contraindicated (see section 4.3).
\*HMG-CoA reductase inhibitors metabolised through CYP3A4 (e.g. simvastatin, lovastatin, and atorvastatin)\*
Posaconazole may substantially increase plasma levels of HMG-CoA reductase inhibitors that are metabolised by CYP3A4. Treatment with these HMG-CoA reductase inhibitors should be discontinued during treatment with posaconazole as increased levels have been associated with rhabdomyolysis (see section 4.3).
\*Vinca alkaloids\*
Most of the vinca alkaloids (e.g. vincristine and vinblastine) are substrates of CYP3A4. Concomitant administration of azole antifungals, including posaconazole, with vincristine has been associated with serious adverse reactions (see section 4.4). Posaconazole may increase the plasma concentrations of vinca alkaloids which may lead to neurotoxicity and other serious adverse reactions. Therefore, reserve azole antifungals, including posaconazole, for patients receiving a vinca alkaloid, including vincristine, who have no alternative antifungal treatment options.
\*Rifabutin\*
Posaconazole increased the Cmax and AUC of rifabutin by 31 % and 72 %, respectively. Concomitant use of posaconazole and rifabutin should be avoided unless the benefit to the patient outweighs the risk (see also above regarding the effect of rifabutin on plasma levels of posaconazole). If these medicinal products are co-administered, careful monitoring of full blood counts and adverse reactions related to increased rifabutin levels (e.g. uveitis) is recommended.
\*Sirolimus\*
Repeat dose administration of posaconazole oral suspension (400 mg twice daily for 16 days) increased the Cmax and AUC of sirolimus (2 mg single dose) an average of 6.7-fold and 8.9-fold (range 3.1 to 17.5-fold), respectively, in healthy subjects. The effect of posaconazole on sirolimus in patients is unknown, but is expected to be variable due to the variable posaconazole exposure in patients. Co-administration of posaconazole with sirolimus is not recommended and should be avoided whenever possible. If it is considered that co-administration is unavoidable, then it is recommended that the dose of sirolimus should be greatly reduced at the time of initiation of posaconazole therapy and that there should be very frequent monitoring of trough concentrations of sirolimus in whole blood. Sirolimus concentrations should be measured upon initiation, during co-administration, and at discontinuation of posaconazole treatment, with sirolimus doses adjusted accordingly. It should be noted that the relationship between sirolimus trough concentration and AUC is changed during co-administration with posaconazole. As a result, sirolimus trough concentrations that fall within the usual therapeutic range may result in sub-therapeutic levels. Therefore, trough concentrations that fall in the upper part of the usual therapeutic range should be targeted and careful attention should be paid to clinical signs and symptoms, laboratory parameters and tissue biopsies.
\*Ciclosporin\*
In heart transplant patients on stable doses of ciclosporin, posaconazole oral suspension 200 mg once daily increased ciclosporin concentrations requiring dose reductions. Cases of elevated ciclosporin levels resulting in serious adverse reactions, including nephrotoxicity and one fatal case of leukoencephalopathy, were reported in clinical efficacy studies. When initiating treatment with posaconazole in patients already receiving ciclosporin, the dose of ciclosporin should be reduced (e.g. to about three quarters of the current dose). Thereafter blood levels of ciclosporin should be monitored carefully during co-administration, and upon discontinuation of posaconazole treatment, and the dose of ciclosporin should be adjusted as necessary.
\*Tacrolimus\*
Posaconazole increased Cmax and AUC of tacrolimus (0.05 mg/kg body weight single dose) by 121 % and 358 %, respectively. Clinically significant interactions resulting in hospitalisation and/or posaconazole discontinuation were reported in clinical efficacy studies. When initiating posaconazole treatment in patients already receiving tacrolimus, the dose of tacrolimus should be reduced (e.g. to about one third of the current dose). Thereafter blood levels of tacrolimus should be monitored carefully during co- administration, and upon discontinuation of posaconazole, and the dose of tacrolimus should be adjusted as necessary.
\*HIV Protease inhibitors\*
As HIV protease inhibitors are CYP3A4 substrates, it is expected that posaconazole will increase plasma levels of these antiretroviral agents. Following co-administration of posaconazole oral suspension (400 mg twice daily) with atazanavir (300 mg once daily) for 7 days in healthy subjects Cmax and AUC of atazanavir increased by an average of 2.6-fold and 3.7-fold (range 1.2 to 26-fold), respectively. Following co-administration of posaconazole oral suspension (400 mg twice daily) with atazanavir and ritonavir (300/100 mg once daily) for 7 days in healthy subjects Cmax and AUC of atazanavir increased by an average of 1.5-fold and 2.5-fold (range 0.9 to 4.1-fold), respectively. The addition of posaconazole to therapy with atazanavir or with atazanavir plus ritonavir was associated with increases in plasma bilirubin levels. Frequent monitoring for adverse reactions and toxicity related to antiretroviral agents that are substrates of CYP3A4 is recommended during co- administration with posaconazole.
\*Midazolam and other benzodiazepines metabolised by CYP3A4\*
In a study in healthy volunteers posaconazole oral suspension (200 mg once daily for 10 days) increased the exposure (AUC) of intravenous midazolam (0.05 mg/kg) by 83 %. In another study in healthy volunteers, repeat dose administration of posaconazole oral suspension (200 mg twice daily for 7 days) increased the Cmax and AUC of intravenous midazolam (0.4 mg single dose) by an average of 1.3- and 4.6-fold (range 1.7 to 6.4-fold), respectively; Posaconazole oral suspension 400 mg twice daily for 7 days increased the intravenous midazolam Cmax and AUC by 1.6 and 6.2-fold (range 1.6 to 7.6- fold), respectively. Both doses of posaconazole increased Cmax and AUC of oral midazolam (2 mg single oral dose) by 2.2 and 4.5-fold, respectively. In addition, posaconazole oral suspension (200 mg or 400 mg) prolonged the mean terminal half-life of midazolam from approximately 3-4 hours to 8-10 hours during co-administration.
Due to the risk of prolonged sedation it is recommended that dose adjustments should be considered when posaconazole is administered concomitantly with any benzodiazepine that is metabolised by CYP3A4 (e.g. midazolam, triazolam, alprazolam) (see section 4.4).
\*Calcium channel blockers metabolised through CYP3A4 (e.g. diltiazem, verapamil, nifedipine, nisoldipine)\*
Frequent monitoring for adverse reactions and toxicity related to calcium channel blockers is recommended during co-administration with posaconazole. Dose adjustment of calcium channel blockers may be required.
\*Digoxin\*
Administration of other azoles has been associated with increases in digoxin levels. Therefore, posaconazole may increase plasma concentration of digoxin and digoxin levels need to be monitored when initiating or discontinuing posaconazole treatment.
\*Sulfonylureas\*
Glucose concentrations decreased in some healthy volunteers when glipizide was co-administered with posaconazole. Monitoring of glucose concentrations is recommended in diabetic patients.
\*All-trans retinoic acid (ATRA) or tretinoin\*
As ATRA is metabolised by the hepatic CYP450 enzymes, notably CYP3A4, concomitant administration with posaconazole, which is a strong inhibitor of CYP3A4, may lead to increased exposure to tretinoin resulting in an increased toxicity (especially hypercalcaemia). Serum calcium levels should be monitored and, if needed, appropriate dose adjustments of tretinoin should be considered during the treatment with posaconazole, and during the following days after treatment.
\*Venetoclax\*
Compared with venetoclax 400 mg administered alone, co-administration of 300 mg posaconazole, a strong CYP3A inhibitor, with venetoclax 50 mg and 100 mg for 7 days in 12 patients, increased venetoclax Cmax to 1.6-fold and 1.9-fold, and AUC to 1.9-fold and 2.4-fold, respectively (see sections 4.3 and 4.4).
Refer to the venetoclax SmPC.
\*\*Paediatric population\*\*
Interaction studies have only been performed in adults.4.6 Fertility, pregnancy and lactation
\*\*Pregnancy\*\*
There is insufficient information on the use of posaconazole in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3). The potential risk for humans is unknown.
Women of childbearing potential have to use effective contraception during treatment. Posaconazole must not be used during pregnancy unless the benefit to the mother clearly outweighs the potential risk to the foetus.
\*\*Breast-feeding\*\*
Posaconazole is excreted into the milk of lactating rats (see section 5.3). The excretion of posaconazole in human breast milk has not been investigated.
Breast-feeding must be stopped on initiation of treatment with posaconazole.
\*\*Fertility\*\*
Posaconazole had no effect on fertility of male rats at doses up to 180 mg/kg (3.4 times the 300-mg tablet based on steady-state plasma concentrations in patients) or female rats at a dose up to 45 mg/kg (2.6 times the 300-mg tablet based on steady- state plasma concentrations in patients). There is no clinical experience assessing the impact of posaconazole on fertility in humans.4.7 Effects on ability to drive and use machines
Since certain adverse reactions (e.g. dizziness, somnolence, etc.) have been reported with posaconazole use, which potentially may affect driving/operating machinery, caution needs to be used.4.8 Undesirable effects
\*\*Summary of the safety profile\*\*
Safety data mainly derive from studies with the oral suspension.
The safety of posaconazole oral suspension has been assessed in > 2,400 patients and healthy volunteers enrolled in clinical studies and from post- marketing experience. The most frequently reported serious related adverse reactions included nausea, vomiting, diarrhoea, pyrexia, and increased bilirubin.
\*\*\*Posaconazole tablets\*\*\*
The safety of posaconazole tablet has been assessed in 104 healthy volunteers and 230 patients enrolled in a clinical study of antifungal prophylaxis.
The safety of posaconazole concentrate for solution for infusion and posaconazole tablet has been assessed in 288 patients enrolled in a clinical study of aspergillosis of whom 161 patients received the concentrate for solution for infusion and 127 patients received the tablet formulation.
The tablet formulation was investigated in AML and MDS patients and those after HSCT with or at risk for Graft versus Host Disease (GVHD) only.
Maximum duration of exposure to the tablet formulation was shorter than with the oral suspension. Plasma exposure resulting from the tablet formulation was higher than observed with the oral suspension.
The safety of posaconazole tablets has been assessed in 230 patients enrolled in the pivotal clinical study. Patients were enrolled in a non-comparative pharmacokinetic and safety study of posaconazole tablets when given as antifungal prophylaxis. Patients were immunocompromised with underlying conditions including haematological malignancy, neutropenia post- chemotherapy, GVHD, and post HSCT. Posaconazole therapy was given for a median duration of 28 days. Twenty patients received 200 mg daily dose and 210 patients received 300 mg daily dose (following twice daily dosing on Day 1 in each cohort).
The safety of posaconazole tablets and concentrate for solution for infusion were also investigated in a controlled study of treatment of invasive aspergillosis. The maximum duration of invasive aspergillosis treatment was similar to that studied with the oral suspension for salvage treatment and was longer than that with the tablets or concentrate for solution for infusion in prophylaxis.
\*\*Tabulated list of adverse reactions\*\*
Within the organ system classes, adverse reactions are listed under headings of frequency using the following categories: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥ 1/10,000 to <1/1,000); very rare (<1/10,000); not known (cannot be estimated from the available data).
\*\*Table 2.\*\* Adverse reactions by body system and frequency reported in clinical studies and/or post-marketing use\\*
| | |
| --- | --- |
| \*\*Blood and lymphatic system disorders\*\* | |
| Common: | neutropenia |
| Uncommon: | thrombocytopenia, leukopenia, anaemia, eosinophilia, lymphadenopathy, splenic infarction |
| Rare: | haemolytic uraemic syndrome, thrombotic thrombocytopenic purpura, pancytopenia, coagulopathy, haemorrhage |
| \*\*Immune system disorders\*\* | |
| Uncommon: | allergic reaction |
| Rare: | hypersensitivity reaction |
| \*\*Endocrine disorders\*\* | |
| Rare: | adrenal insufficiency, blood gonadotropin decreased, pseudoaldosteronism |
| \*\*Metabolism and nutrition disorders\*\* | |
| Common: | electrolyte imbalance, anorexia, decreased appetite, hypokalaemia, hypomagnesaemia |
| Uncommon: | hyperglycaemia, hypoglycaemia |
| \*\*Psychiatric disorders\*\* | |
| Uncommon: | abnormal dreams, confusional state, sleep disorder |
| Rare: | psychotic disorder, depression |
| \*\*Nervous system disorders\*\* | |
| Common: | paraesthesia, dizziness, somnolence, headache, dysgeusia |
| Uncommon: | convulsions, neuropathy, hypoaesthesia, tremor, aphasia, insomnia |
| Rare: | cerebrovascular accident, encephalopathy, peripheral neuropathy, syncope |
| \*\*Eye disorders\*\* | |
| Uncommon: | blurred vision, photophobia, visual acuity reduced |
| Rare: | diplopia, scotoma |
| \*\*Ear and labyrinth disorder\*\* | |
| Rare: | hearing impairment |
| \*\*Cardiac disorders\*\* | |
| Uncommon: | long QT syndrome§, electrocardiogram abnormal§, palpitations, bradycardia, supraventricular extrasystoles, tachycardia |
| Rare: | torsade de pointes, sudden death, ventricular tachycardia, cardio-respiratory arrest, cardiac failure, myocardial infarction |
| \*\*Vascular disorders\*\* | |
| Common: | hypertension |
| Uncommon: | hypotension, vasculitis |
| Rare: | pulmonary embolism, deep vein thrombosis |
| \*\*Respiratory, thoracic and mediastinal disorders\*\* | |
| Uncommon: | cough, epistaxis, hiccups, nasal congestion, pleuritic pain, tachypnoea |
| Rare: | pulmonary hypertension, interstitial pneumonia, pneumonitis |
| \*\*Gastrointestinal disorders\*\* | |
| Very Common: | nausea |
| Common: | vomiting, abdominal pain, diarrhoea, dyspepsia, dry mouth, flatulence, constipation, anorectal discomfort |
| Uncommon: | pancreatitis, abdominal distension, enteritis, epigastric discomfort, eructation, gastroesophageal reflux disease, oedema mouth |
| Rare: | gastrointestinal haemorrhage, ileus |
| \*\*Hepatobiliary disorders\*\* | |
| Common: | liver function tests raised (ALT increased, AST increased, bilirubin increased, alkaline phosphatase increased, GGT increased) |
| Uncommon: | hepatocellular damage, hepatitis, jaundice, hepatomegaly, cholestasis, hepatic toxicity, hepatic function abnormal |
| Rare: | hepatic failure, hepatitis cholestatic, hepatosplenomegaly, liver tenderness, asterixis |
| \*\*Skin and subcutaneous tissue disorders\*\* | |
| Common: | rash, pruritis |
| Uncommon: | mouth ulceration, alopecia, dermatitis, erythema, petechiae |
| Rare: | Stevens Johnson syndrome, vesicular rash |
| Not known | Photosensitivity reaction§ |
| \*\*Musculoskeletal and connective tissue disorders\*\* | |
| Uncommon: | back pain, neck pain, musculoskeletal pain, pain in extremity |
| \*\*Renal and urinary disorders\*\* | |
| Uncommon: | acute renal failure, renal failure, blood creatinine increased |
| Rare: | renal tubular acidosis, interstitial nephritis |
| \*\*Reproductive system and breast disorders\*\* | |
| Uncommon: | menstrual disorder |
| Rare: | breast pain |
| \*\*General disorders and administration site conditions\*\* | |
| Common: | pyrexia (fever), asthenia, fatigue |
| Uncommon: | oedema, pain, chills, malaise, chest discomfort, drug intolerance, feeling jittery, mucosal inflammation |
| Rare: | tongue oedema, face oedema |
| \*\*Investigations\*\* | |
| Uncommon: | altered medicine levels, blood phosphorus decreased, chest x-ray abnormal |
\\* Based on adverse reactions observed with the oral suspension, gastro- resistant tablets, concentrate for solution for infusion, and gastro-resistant powder and solvent for oral suspension.
§ See section 4.4.
\*\*Description of selected adverse reactions\*\*
\*Hepatobiliary disorders\*
During post-marketing surveillance of posaconazole oral suspension, severe hepatic injury with fatal outcome has been reported (see section 4.4).
\*\*Reporting of suspected adverse reactions\*\*
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.4.9 Overdose
There is no experience with overdose of posaconazole tablets.
During clinical studies, patients who received posaconazole oral suspension doses up to 1,600 mg/day experienced no different adverse reactions from those reported with patients at the lower doses.
Accidental overdose was noted in one patient who took posaconazole oral suspension 1,200 mg twice a day for 3 days. No adverse reactions were noted by the investigator.
Posaconazole is not removed by haemodialysis. There is no special treatment available in the case of overdose with posaconazole. Supportive care may be considered.
## Pharmacological Properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antimycotics for systemic use, triazole derivatives, ATC code: J02AC04.
\*\*Mechanism of action\*\*
Posaconazole inhibits the enzyme lanosterol 14α-demethylase (CYP51), which catalyses an essential step in ergosterol biosynthesis.
\*\*Microbiology\*\*
Posaconazole has been shown \*in vitro\* to be active against the following microorganisms: \*Aspergillus\* species (\*Aspergillus fumigatus, A. flavus, A. terreus, A. nidulans, A. niger, A. ustus\*)\*, Candida\* species (\*Candida albicans,\* \*C. glabrata, C. krusei, C. parapsilosis, C. tropicalis, C. dubliniensis, C. famata, C. inconspicua, C. lipolytica, C. norvegensis, C. pseudotropicalis\*), \*Coccidioides immitis, Fonsecaea pedrosoi,\* and species of \*Fusarium, Rhizomucor, Mucor\*, and \*Rhizopus\*. The microbiological data suggest that posaconazole is active against \*Rhizomucor, Mucor,\* and \*Rhizopus;\* however, the clinical data are currently too limited to assess the efficacy of posaconazole against these causative agents.
The following \*in vitro\* data are available, but their clinical significance is unknown. In a surveillance study of > 3,000 clinical mold isolates from 2010- 2018, 90 % of non-\*Aspergillus\* fungi exhibited the following \*in vitro\* minimum inhibitory concentration (MIC): \*Mucorales\* spp (n=81) of 2 mg/L; \*Scedosporium apiospermum/S. boydii\* (n=65) of 2 mg/L; \*Exophiala dermatiditis\* (n=15) of 0.5 mg/L, and \*Purpureocillium lilacinum\* (n=21) of 1 mg/L.
\*\*Resistance\*\*
Clinical isolates with decreased susceptibility to posaconazole have been identified. The principle mechanism of resistance is the acquisition of substitutions in the target protein, CYP51.
\*\*Epidemiological Cut-off (ECOFF) Values for\*\* \*\*\*Aspergillus spp\*\*\*\*\*.\*\*
The ECOFF values for posaconazole, which distinguish the wild type population from isolates with acquired resistance, have been determined by EUCAST methodology.
EUCAST ECOFF values:
• \*Aspergillus flavus\*: 0.5 mg/L
• \*Aspergillus fumigatus\*: 0.5 mg/L
• \*Aspergillus nidulans\*: 0.5 mg/L
• \*Aspergillus niger\*: 0.5 mg/L
• \*Aspergillus terreus\*: 0.25 mg/L
There are currently insufficient data to set clinical breakpoints for \*Aspergillus\* spp. ECOFF values do not equate to clinical breakpoints.
\*\*Breakpoints\*\*
EUCAST MIC breakpoints for posaconazole [susceptible (S); resistant (R)]:
• \*Candida albicans\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida tropicalis\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida parapsilosis\*: S ≤0.06 mg/L, R >0.06 mg/L
• \*Candida dubliniensis\*: S ≤0.06 mg/L, R > 0.06 mg/L
There are currently insufficient data to set clinical breakpoints for other \*Candida\* species.
\*\*Combination with other antifungal agents\*\*
The use of combination antifungal therapies should not decrease the efficacy of either posaconazole or the other therapies; however, there is currently no clinical evidence that combination therapy will provide an added benefit.
\*\*Clinical experience\*\*
\*\*\*Summary of posaconazole concentrate for solution for infusion and tablet\*\* \*\*study invasive aspergillosis\*\*\*
The safety and efficacy of posaconazole for the treatment of patients with invasive aspergillosis was evaluated in a double-blind controlled study (study- 69) in 575 patients with proven, probable, or possible invasive fungal infections per EORTC/MSG criteria.
Patients were treated with posaconazole (n=288) concentrate for solution for infusion or tablet given at a dose of 300 mg QD (BID on Day 1). Comparator patients were treated with voriconazole (n=287) given IV at a dose of 6 mg/kg BID Day 1 followed by 4 mg/kg BID, or orally at a dose of 300 mg BID Day 1 followed by 200 mg BID. Median treatment duration was 67 days (posaconazole) and 64 days (voriconazole).
In the intent-to-treat (ITT) population (all subjects who received at least one dose of study drug), 288 patients received posaconazole and 287 patients received voriconazole. The full analysis set population (FAS) is the subset of all subjects within the ITT population who were classified by independent adjudication as having proven or probable invasive aspergillosis: 163 subjects for posaconazole and 171 subjects for voriconazole. The all-cause mortality and global clinical response in these two populations are presented in Table 3 and 4, respectively.
\*\*Table 3.\*\* Posaconazole invasive aspergillosis treatment study 1: all-cause mortality at Day 42 and Day 84, in the ITT and FAS populations
| | | | | | |
| --- | --- | --- | --- | --- | --- |
| | \*\*Posaconazole\*\* | | \*\*Voriconazole\*\* | | |
| Population | N | n (%) | N | n (%) | Difference\\* (95% CI) |
| Mortality in ITT at Day 42 | 288 | 44 (15.3) | 287 | 59 (20.6) | -5.3 % (-11.6, 1.0) |
| Mortality in ITT at Day 84 | 288 | 81 (28.1) | 287 | 88 (30.7) | -2.5 % (-9.9, 4.9) |
| Mortality in FAS at Day 42 | 163 | 31 (19.0) | 171 | 32 (18.7) | 0.3% (-8.2, 8.8) |
| Mortality in FAS at Day 84 | 163 | 56 (34.4) | 171 | 53 (31.0) | 3.1% (-6.9, 13.1) |
| \\* Adjusted treatment difference based on Miettinen and Nurminen's method stratified by randomisation factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme. | | | | | |
\*\*Table 4.\*\* Posaconazole invasive aspergillosis treatment study 1: global clinical response at Week 6 and Week 12 in the FAS population
| | | | | | |
| --- | --- | --- | --- | --- | --- |
| | \*\*Posaconazole\*\* | | \*\*Voriconazole\*\* | | |
| Population | N | Success (%) | N | Success (%) | Difference\\* (95 %CI) |
| Global clinical response in the FAS at 6 weeks | 163 | 73 (44.8) | 171 | 78 (45.6) | -0.6 % (-11.2, 10.1) |
| Global clinical response in the FAS at 12 weeks | 163 | 69 (42.3) | 171 | 79 (46.2) | -3.4 % (-13.9, 7.1) |
| \\* Successful Global Clinical Response was defined as survival with a partial or complete response Adjusted treatment difference based on Miettinen and Nurminen's method stratified by randomisation factor (risk for mortality/poor outcome), using Cochran-Mantel-Haenszel weighting scheme. | | | | | |
\*\*\*Summary of posaconazole tablet bridging study\*\*\*
Study 5615 was a non-comparative multi-centre study performed to evaluate the pharmacokinetic properties, safety, and tolerability of posaconazole tablet. Study 5615 was conducted in a similar patient population to that previously studied in the pivotal posaconazole oral suspension clinical program. The pharmacokinetics and safety data from Study 5615 were bridged to the existing data (including efficacy data) with the oral suspension.
The subject population included: 1) patients with AML or MDS who had recently received chemotherapy and had developed or were anticipated to develop significant neutropenia, or 2) patients who had undergone a HSCT and were receiving immunosuppressive therapy for prevention or treatment of GVHD. Two different dosing groups were evaluated: 200 mg twice daily on Day 1, followed by 200 mg once daily thereafter (Part IA) and 300 mg twice daily on Day 1, followed by 300 mg once daily thereafter (Part 1B and Part 2).
Serial PK samples were collected on Day 1 and at steady-state on Day 8 for all Part 1 subjects and a subset of Part 2 subjects. Moreover, sparse PK samples were collected at several days during steady state before the next dose (Cmin) for a larger subject population. Based on average Cmin concentrations, a predicted average concentration (Cav) could be calculated for 186 subjects dosed with 300 mg. PK analysis in patients of Cav found that 81 % of the subjects treated with the 300 mg once daily dose attained steady state predicted Cav between 500-2,500 ng/mL. One subject (<1 %) had a predicted Cav below 500 ng/mL and 19 % of the subjects had a predicted Cav above 2,500 ng/mL. Subjects achieved a mean predicted Cav at steady state of 1,970 ng/mL.
In Table 5 a comparison is shown of exposure (Cav) after administration of posaconazole tablet and posaconazole oral suspension at therapeutic doses in patients depicted as quartile analysis. Exposures after tablet administration are generally higher than, but overlapping with, exposures after administration of posaconazole oral suspension.
\*\*Table 5.\*\* Cav quartile analyses of pivotal patient studies with posaconazole tablet and oral suspension
| | | | | |
| --- | --- | --- | --- | --- |
| | \*\*Posaconazole tablet\*\* | \*\*Posaconazole oral suspension\*\* | | |
| \*\*Prophylaxis in AML and HSCT Study 5615\*\* | \*\*Prophylaxis in GVHD Study 316\*\* | \*\*Prophylaxis in Neutropenia Study 1899\*\* | \*\*Treatment - Invasive Aspergillosis Study 0041\*\* |
| \*\*300 mg once daily (Day 1 300 mg twice daily)\\*\*\* | \*\*200 mg three times daily\*\* | \*\*200 mg three times daily\*\* | \*\*200 mg four times daily (hospitalized) then 400 mg twice daily\*\* |
| \*\*Quartile\*\* | \*\*pCav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* | \*\*Cav Range\*\* \*\*(ng/mL)\*\* |
| Q1 | 442 – 1,223 | 22 – 557 | 90 – 322 | 55 – 277 |
| Q2 | 1,240 – 1,710 | 557 – 915 | 322 – 490 | 290 – 544 |
| Q3 | 1,719 – 2,291 | 915 – 1,563 | 490 – 734 | 550 – 861 |
| Q4 | 2,304 – 9,523 | 1,563 – 3,650 | 734 – 2,200 | 877 – 2,010 |
| pCav: predicted Cav Cav = the average concentration when measured at steady state \\*20 patients received 200 mg once daily (Day 1 200 mg twice daily) | | | | |
\*\*\*Summary of posaconazole oral suspension studies\*\*\*
\*Invasive aspergillosis\*
Oral posaconazole suspension 800 mg/day in divided doses was evaluated for the treatment of invasive aspergillosis in patients with disease refractory to amphotericin B (including liposomal formulations) or itraconazole or in patients who were intolerant of these medicinal products in a non-comparative salvage therapy study (Study 0041). Clinical outcomes were compared with those in an external control group derived from a retrospective review of medical records. The external control group included 86 patients treated with available therapy (as above) mostly at the same time and at the same sites as the patients treated with posaconazole. Most of the cases of aspergillosis were considered to be refractory to prior therapy in both the posaconazole group (88%) and in the external control group (79 %).
As shown in Table 6, a successful response (complete or partial resolution) at the end of treatment was seen in 42 % of posaconazole-treated patients compared to 26 % of the external group. However, this was not a prospective, randomised controlled study and so all comparisons with the external control group should be viewed with caution.
\*\*Table 6.\*\* Overall efficacy of posaconazole oral suspension at the end of treatment for invasive aspergillosis in comparison to an external control group
| | | | | |
| --- | --- | --- | --- | --- |
| | \*\*Posaconazole oral suspension\*\* | | \*\*External control group\*\* | |
| Overall Response | 45/107 (42 %) | | 22/86 (26 %) | |
| \*\*Success by Species\*\* All mycologically confirmed \*Aspergillus spp.2\* | 34/76 | (45 %) | 19/74 | (26 %) |
| \*A. fumigatus\* | 12/29 | (41 %) | 12/34 | (35 %) |
| \*A. flavus\* | 10/19 | (53 %) | 3/16 | (19 %) |
| \*A. terreus\* | 4/14 | (29 %) | 2/13 | (15 %) |
| \*A. niger\* | 3/5 | (60 %) | 2/7 | (29 %) |
2 Includes other less common species or species unknown
\*Fusarium spp.\*
11 of 24 patients who had proven or probable fusariosis were successfully treated with posaconazole oral suspension 800 mg/day in divided doses for a median of 124 days and up to 212 days. Among eighteen patients who were intolerant or had infections refractory to amphotericin B or itraconazole, seven patients were classed as responders.
\*Chromoblastomycosis/Mycetoma\*
9 of 11 patients were successfully treated with posaconazole oral suspension 800 mg/day in divided doses for a median of 268 days and up to 377 days. Five of these patients had chromoblastomycosis due to \*Fonsecaea pedrosoi\* and 4 had mycetoma, mostly due to \*Madurella\* species.
\*Coccidioidomycosis\*
11 of 16 patients were successfully treated (at the end of treatment complete or partial resolution of signs and symptoms present at baseline) with posaconazole oral suspension 800 mg/day in divided doses for a median of 296 days and up to 460 days.
\*Prophylaxis of Invasive Fungal Infections (IFIs) (Studies 316 and 1899)\*
Two randomised, controlled prophylaxis studies were conducted among patients at high-risk for developing invasive fungal infections.
Study 316 was a randomised, double-blind study of posaconazole oral suspension (200 mg three times a day) versus fluconazole capsules (400 mg once daily) in allogeneic hematopoietic stem cell transplant recipients with graft-versus-host disease (GVHD). The primary efficacy endpoint was the incidence of proven/probable IFIs at 16 weeks post-randomisation as determined by an independent, blinded external expert panel. A key secondary endpoint was the incidence of proven/probable IFIs during the on-treatment period (first dose to last dose of study medicinal product + 7 days). The majority (377/600, [63 %]) of patients included had Acute Grade 2 or 3 or chronic extensive (195/600, [32.5 %]) GVHD at study start. The mean duration of therapy was 80 days for posaconazole and 77 days for fluconazole.
Study 1899 was a randomised, evaluator-blinded study of posaconazole oral suspension (200 mg three times a day) versus fluconazole suspension (400 mg once daily) or itraconazole oral solution (200 mg twice a day) in neutropenic patients who were receiving cytotoxic chemotherapy for acute myelogenous leukaemia or myelodysplastic syndromes. The primary efficacy endpoint was the incidence of proven/probable IFIs as determined by an independent, blinded external expert panel during the on-treatment period. A key secondary endpoint was the incidence of proven/probable IFIs at 100 days post- randomisation. New diagnosis of acute myelogenous leukaemia was the most common underlying condition (435/602, [72 %]). The mean duration of therapy was 29 days for posaconazole and 25 days for fluconazole/itraconazole.
In both prophylaxis studies, aspergillosis was the most common breakthrough infection. See Table 7 and 8 for results from both studies. There were fewer breakthrough \*Aspergillus\* infections in patients receiving posaconazole prophylaxis when compared to control patients.
\*\*Table 7.\*\* Results from clinical studies in prophylaxis of Invasive Fungal Infections
| | | | |
| --- | --- | --- | --- |
| \*\*Study\*\* | \*\*Posaconazole oral suspension\*\* | \*\*Controla\*\* | \*\*P-Value\*\* |
| \*\*Proportion (%) of patients with proven/probable IFIs\*\* | | | |
| \*\*On-treatment periodb\*\* | | | |
| 1899d | 7/304 (2) | 25/298 (8) | 0.0009 |
| 316e | 7/291 (2) | 22/288 (8) | 0.0038 |
| \*\*Fixed-time periodc\*\* | | | |
| 1899d | 14/304 (5) | 33/298 (11) | 0.0031 |
| 316d | 16/301 (5) | 27/299 (9) | 0.0740 |
FLU = fluconazole; ITZ = itraconazole; POS = posaconazole.
a: FLU/ITZ (1899); FLU (316).
b: In 1899 this was the period from randomisation to last dose of study medicinal product plus 7 days; in 316 it was the period from first dose to last dose of study medicinal product plus 7 days.
c: In 1899, this was the period from randomisation to 100 days post- randomisation; in 316 it was the period from the baseline day to 111 days post-baseline.
d: All randomised
e: All treated
\*\*Table 8.\*\* Results from clinical studies in prophylaxis of Invasive Fungal Infections
| | | |
| --- | --- | --- |
| \*\*Study\*\* | \*\*Posaconazole oral suspension\*\* | \*\*Controla\*\* |
| \*\*Proportion (%) of patients with proven/probable Aspergillosis\*\* | | |
| \*\*On-treatment periodb\*\* | | |
| 1899d | 2/304 (1) | 20/298 (7) |
| 316e | 3/291 (1) | 17/288 (6) |
| \*\*Fixed-time periodc\*\* | | |
| 1899d | 4/304 (1) | 26/298 (9) |
| 316d | 7/301 (2) | 21/299 (7) |
FLU = fluconazole; ITZ = itraconazole; POS = posaconazole.
a: FLU/ITZ (1899); FLU (316).
b: In 1899 this was the period from randomisation to last dose of study medicinal product plus 7 days; in 316 it was the period from first dose to last dose of study medicinal product plus 7 days.
c: In 1899, this was the period from randomisation to 100 days post- randomisation; in 316 it was the period from the baseline day to 111 days post-baseline.
d: All randomised
e: All treated
In Study 1899, a significant decrease in all cause mortality in favour of posaconazole was observed [POS 49/304 (16 %) vs. FLU/ITZ 67/298 (22 %) p= 0.048]. Based on Kaplan-Meier estimates, the probability of survival up to day 100 after randomisation, was significantly higher for posaconazole recipients; this survival benefit was demonstrated when the analysis considered all causes of death (P= 0.0354) as well as IFI-related deaths (P = 0.0209).
In Study 316, overall mortality was similar (POS, 25 %; FLU, 28 %); however, the proportion of IFI-related deaths was significantly lower in the POS group (4/301) compared with the FLU group (12/299; P= 0.0413).
\*\*Paediatric population\*\*
There is limited paediatric experience for posaconazole tablets.
Three patients 14-17 years of age were treated with posaconazole concentrate for solution for infusion and tablet 300 mg/day (BID on Day 1 followed by QD thereafter) in the study of treatment of invasive aspergillosis.
The safety and efficacy of posaconazole (posaconazole gastro-resistant powder and solvent for oral suspension; posaconazole concentrate for solution for infusion) have been established in paediatric patients 2 to less than 18 years of age. Use of posaconazole in these age groups is supported by evidence from adequate and well-controlled studies of posaconazole in adults and pharmacokinetic and safety data from paediatric studies (see section 5.2). No new safety signals associated with the use of posaconazole in paediatric patients were identified in the paediatric studies (see section 4.8).
Safety and efficacy in paediatric patients below the age of 2 years have not been established.
No data are available.
\*\*Electrocardiogram evaluation\*\*
Multiple, time-matched ECGs collected over a 12 hour period were obtained before and during administration of posaconazole oral suspension (400 mg twice daily with high fat meals) from 173 healthy male and female volunteers aged 18 to 85 years. No clinically relevant changes in the mean QTc (Fridericia) interval from baseline were observed.5.2 Pharmacokinetic properties
\*\*Pharmacokinetic / Pharmacodynamic relationships\*\*
A correlation between total medicinal product exposure divided by MIC (AUC/MIC) and clinical outcome was observed. The critical ratio for subjects with \*Aspergillus\* infections was ~200. It is particularly important to try to ensure that maximal plasma levels are achieved in patients infected with \*Aspergillus\* (see sections 4.2 and 5.2 on recommended dose regimens).
\*\*Absorption\*\*
Posaconazole tablets are absorbed with a median Tmax of 4 to 5 hours and exhibits dose proportional pharmacokinetics after single and multiple dosing up to 300 mg.
Following a single dose administration of 300 mg posaconazole Amarox tablets after a high fat meal to healthy volunteers, the AUC0-72 hours and Cmax were higher compared to administration under fasted condition (51 % and 16% for AUC0-72 hours and Cmax respectively). Based on a population pharmacokinetic model, posaconazole Cav is increased 20 % when given with a meal compared to a fasted state.
Posaconazole plasma concentrations following administration of posaconazole tablets may increase over time in some patients. The reason for this time- dependency is not completely understood.
\*\*Distribution\*\*
Posaconazole, after administration of the tablet, has a mean apparent volume of distribution of 394 L (42 %), ranging between 294-583 L among the studies in healthy volunteers.
Posaconazole is highly protein bound (> 98 %), predominantly to serum albumin.
\*\*Biotransformation\*\*
Posaconazole does not have any major circulating metabolites and its concentrations are unlikely to be altered by inhibitors of CYP450 enzymes. Of the circulating metabolites, the majority are glucuronide conjugates of posaconazole with only minor amounts of oxidative (CYP450 mediated) metabolites observed. The excreted metabolites in urine and faeces account for approximately 17 % of the administered radiolabelled dose.
\*\*Elimination\*\*
Posaconazole after administration of the tablets, is slowly eliminated with a mean half-life (t½) of 29 hours (range 26 to 31 hours) and a mean apparent clearance ranging from 7.5 to 11 L/hr. After administration of 14C- posaconazole, radioactivity was predominantly recovered in the faeces (77 % of the radiolabelled dose) with the major component being parent compound (66 % of the radiolabelled dose). Renal clearance is a minor elimination pathway, with 14 % of the radiolabelled dose excreted in urine (< 0.2 % of the radiolabelled dose is parent compound). Steady-state plasma concentrations are attained by Day 6 at the 300 mg dose (once daily after twice daily loading dose at Day 1).
\*\*Pharmacokinetics in special populations\*\*
Based on a population pharmacokinetic model evaluating posaconazole pharmacokinetics, steady state posaconazole concentrations were predicted in patients administered posaconazole concentrate for solution for infusion or tablets 300 mg once a day following BID dosing on Day 1 for the treatment of invasive aspergillosis and prophylaxis of invasive fungal infections.
\*\*Table 9.\*\* Population predicted median (10th percentile, 90th percentile) posaconazole steady state plasma concentrations in patients following administration of posaconazole concentrate for solution for infusion or tablets 300 mg QD (BID on Day 1)
| | | | |
| --- | --- | --- | --- |
| \*\*Regimen\*\* | \*\*Population\*\* | \*\*Cav (ng/mL)\*\* | \*\*Cmin (ng/mL)\*\* |
| Tablet-(Fasted) | Prophylaxis | 1,550 (874; 2,690) | 1,330 (667; 2,400) |
| Treatment of Invasive Aspergillosis | 1,490 (663; 3,230) | 1,780 (879; 3,540) |
| Concentrate for Solution for Infusion | Prophylaxis | 1,890 (1,100; 3,150) | 1,500 (745; 2,660) |
| Treatment of Invasive Aspergillosis | 2,240 (1,230; 4,160) | 1,780 (874; 3,620) |
The population pharmacokinetic analysis of posaconazole in patients suggests that race, sex, renal impairment and disease (prophylaxis or treatment) have no clinically meaningful effect on the pharmacokinetics of posaconazole.
\*Children (< 18 years)\*
There is limited (n=3) paediatric experience with posaconazole tablets.
The pharmacokinetics of posaconazole oral suspension have been evaluated in paediatric patients.
Following administration of 800 mg per day of posaconazole oral suspension as a divided dose for treatment of invasive fungal infections, mean trough plasma concentrations from 12 patients 8 - 17 years of age (776 ng/mL) were similar to concentrations from 194 patients 18 - 64 years of age (817 ng/mL). No pharmacokinetic data are available from paediatric patients less than 8 years of age.
Similarly, in the prophylaxis studies, the mean steady-state posaconazole average concentration (Cav) was comparable among ten adolescents (13-17 years of age) to Cav achieved in adults (≥ 18 years of age).
\*Gender\*
The pharmacokinetics of posaconazole tablets are comparable in men and women.
\*Elderly\*
No overall differences in safety were observed between the geriatric patients and younger patients.
The population pharmacokinetic model of posaconazole concentrate for solution for infusion and tablets indicates that posaconazole clearance is related to age. Posaconazole Cav is generally comparable between young and elderly patients (≥ 65 years of age); however, the Cav is increased by 11 % in the very elderly (≥ 80 years). It is, therefore, suggested to closely monitor very elderly patients (≥ 80 years) for adverse events.
The pharmacokinetics of posaconazole tablets are comparable in young and elderly subjects (≥ 65 years of age).
Pharmacokinetic differences based upon age are not considered to be clinically relevant; therefore, no dose adjustment is required.
\*Race\*
There is insufficient data among different races with posaconazole tablets.
There was a slight decrease (16 %) in the AUC and Cmax of posaconazole oral suspension in Black subjects relative to Caucasian subjects. However, the safety profile of posaconazole between the Black and Caucasian subjects was similar.
\*Weight\*
The population pharmacokinetic model of posaconazole concentrate for solution for infusion and tablets indicates that posaconazole clearance is related to weight. In patients > 120 kg, the Cav is decreased by 25 % and in patients <50 kg, the Cav is increased by 19 %. It is, therefore, suggested to closely monitor for breakthrough fungal infections in patients weighing more than 120 kg.
\*Renal impairment\*
Following single-dose administration of posaconazole oral suspension, there was no effect of mild and moderate renal impairment (n=18, Cl cr ≥ 20 mL/min/1.73 m2) on posaconazole pharmacokinetics; therefore, no dose adjustment is required. In subjects with severe renal impairment (n=6, Cl cr < 20 mL/min/1.73 m2), the AUC of posaconazole was highly variable [> 96 % CV (coefficient of variance)] compared to other renal groups [< 40 % CV]. However, as posaconazole is not significantly renally eliminated, an effect of severe renal impairment on the pharmacokinetics of posaconazole is not expected and no dose adjustment is recommended. Posaconazole is not removed by haemodialysis.
Similar recommendations apply to posaconazole tablets; however, a specific study has not been conducted with the posaconazole tablets.
\*Hepatic impairment\*
After a single oral dose of 400 mg posaconazole oral suspension to patients with mild (Child-Pugh Class A), moderate (Child-Pugh Class B) or severe (Child-Pugh Class C) hepatic impairment (six per group), the mean AUC was 1.3 to 1.6-fold higher compared to that for matched control subjects with normal hepatic function. Unbound concentrations were not determined and it cannot be excluded that there is a larger increase in unbound posaconazole exposure than the observed 60 % increase in total AUC. The elimination half- life (t1/2) was prolonged from approximately 27 hours up to ~43 hours in respective groups. No dose adjustment is recommended for patients with mild to severe hepatic impairment but caution is advised due to the potential for higher plasma exposure.
Similar recommendations apply to posaconazole tablets; however, a specific study has not been conducted with the posaconazole tablets.5.3 Preclinical safety data
As observed with other azole antifungal agents, effects related to inhibition of steroid hormone synthesis were seen in repeated-dose toxicity studies with posaconazole. Adrenal suppressive effects were observed in toxicity studies in rats and dogs at exposures equal to or greater than those obtained at therapeutic doses in humans.
Neuronal phospholipidosis occurred in dogs dosed for ≥ 3 months at lower systemic exposures than those obtained at therapeutic doses in humans. This finding was not seen in monkeys dosed for one year. In twelve-month neurotoxicity studies in dogs and monkeys, no functional effects were observed on the central or peripheral nervous systems at systemic exposures greater than those achieved therapeutically.
Pulmonary phospholipidosis resulting in dilatation and obstruction of the alveoli was observed in the 2-year study in rats. These findings are not necessarily indicative of a potential for functional changes in humans.
No effects on electrocardiograms, including QT and QTc intervals, were seen in a repeat dose safety pharmacology study in monkeys at maximal plasma concentrations 8.5-fold greater than the concentrations obtained at therapeutic doses in humans. Echocardiography revealed no indication of cardiac decompensation in a repeat dose safety pharmacology study in rats at a systemic exposure 2.1-fold greater than that achieved therapeutically. Increased systolic and arterial blood pressures (up to 29 mm-Hg) were seen in rats and monkeys at systemic exposures 2.1-fold and 8.5-fold greater, respectively, than those achieved with the human therapeutic doses.
Reproduction, peri- and postnatal development studies were conducted in rats. At exposures lower than those obtained at therapeutic doses in humans, posaconazole caused skeletal variations and malformations, dystocia, increased length of gestation, reduced mean litter size and postnatal viability. In rabbits, posaconazole was embryotoxic at exposures greater than those obtained at therapeutic doses. As observed with other azole antifungal agents, these effects on reproduction were considered to be due to a treatment-related effect on steroidogenesis.
Posaconazole was not genotoxic in \*in vitro\* and \*in vivo\* studies. Carcinogenicity studies did not reveal special hazards for humans.
In a nonclinical study using intravenous administration of posaconazole in very young dogs (dosed from 2-8 weeks of age) an increase in the incidence of brain ventricle enlargement was observed in treated animals as compared with concurrent control animals. No difference in the incidence of brain ventricle enlargement between control and treated animals was observed following the subsequent 5 month treatment-free period. There were no neurologic, behavioural or developmental abnormalities in the dogs with this finding, and a similar brain finding was not seen with either oral posaconazole administration to juvenile dogs (4 days to 9 months of age) or intravenous posaconazole administration to juvenile dogs (10 weeks to 23 weeks of age). The clinical significance of this finding is unknown.
## Pharmaceutical Particulars
6.1 List of excipients
\*\*Tablet core:\*\*
Hypromellose acetate succinate
Cellulose, microcrystalline
Hydroxypropylcellulose
Croscarmellose sodium
Silica, colloidal anhydrous
Magnesium stearate
\*\*Film coating:\*\*
Polyvinyl alcohol-part. hydrolyzed (E1203)
Titanium dioxide (E171)
Macrogol (E1521)
Talc (E553b)
Iron oxide yellow (E172)
Iron oxide red (E172)6.2 Incompatibilities
Not applicable.6.3 Shelf life
3 years6.4 Special precautions for storage
This medicinal product does not require any special storage conditions6.5 Nature and contents of container
White Opaque PVC/Aclar-Alu blister pack of 24 and 96 tablets.
Not all pack sizes may be marketed.6.6 Special precautions for disposal and other handling
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
