Study in Healthy Male Subjects to Evaluate the Effect of Itraconazole and Rifampicin on the PK of Fedovapagon
- Registration Number
- NCT02440841
- Lead Sponsor
- Vantia Ltd
- Brief Summary
The purpose of this study is to investigate the potential for co-administration of strong inhibitors or inducers of CYP3A4 to alter the pharmacokinetics of fedovapagon.
- Detailed Description
Fedovapagon is a vasopressin V2 receptor agonist in development for the treatment of nocturia. Agonism of the V2 receptor, located in the collecting ducts of the kidney, leads to translocation of aquaporin channels and increased re absorption of water and anti-diuresis.
A number of drugs that are commonly co-prescribed in the population who may present for treatment of nocturia are inhibitors of CYP3A4, including diltiazem, verapamil, erythromycin and clarithromycin and may therefore impact the plasma levels of fedovapagon if co administered.
Conversely, concomitant intake of drugs that are potent CYP3A4 inducers may lead to lower than anticipated plasma concentrations of fedovapagon thus reducing the efficacy of fedovapagon. It is therefore important to assess the effect of CYP3A4 induction on the pharmacokinetic (PK) parameters of fedovapagon.
The study design uses itraconazole as a potent inhibitor of CYP3A4 and, in a separate cohort of subjects, rifampicin as a potent CYP3A4 inducer at doses intended to maximize the potential to demonstrate an interaction.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 29
- Healthy males aged 18 to 45
- Have a body mass index between 18 and 29.9 kg/m2 (weight: ≥50 kg and ≤100 kg)
- No clinically significant medical history
- Ability to comply with the requirements of the study
- Provide written informed consent
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) should be below or equal to upper level of normal (ULN). Otherwise liver enzymes should show no clinical significant abnormalities. Total bilirubin should not exceed 1.5 x ULN. Liver enzymes will be re-tested only once before randomization if required.
- Be judged by the Investigator to be in good health based on medical history (in particular, no congestive heart failure, ischemic heart disease, valvular heart disease, significant pulmonary disease, renal failure, edematous disorder, liver disease, gastric disorders, porphyria, diabetes mellitus or hereditary disorders of carbohydrate metabolism), physical examination, vital sign measurements and laboratory safety tests
- Agree to refrain from the consumption of grapefruit or grapefruit juice, apple or orange juice, vegetables from the mustard green family (e.g., kale, broccoli, watercress, collard greens, kohlrabi, brussels sprouts, mustard) and charbroiled meats containing products beginning 1 week prior to administration of the initial administration of trial drug, throughout the trial
- Use of any prescribed medication or St John's Wort within 14 days (or 5 half-lives if this is longer) or over-the-counter medication (except paracetamol) within 1 week of dosing. Specific medication not to be taken within 2 weeks of (before or after) administration of itraconazole is described in the Summary of Product Characteristic for Sempera®
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description fedovapagon and rifampicin rifampicin Two daily doses of fedovapagon and once daily doses of rifampicin fedovapagon and rifampicin fedovapagon Two daily doses of fedovapagon and once daily doses of rifampicin fedovapagon and itraconazole Itraconazole Two daily doses of fedovapagon and once daily doses of itraconazole fedovapagon and itraconazole fedovapagon Two daily doses of fedovapagon and once daily doses of itraconazole
- Primary Outcome Measures
Name Time Method Plasma fedovapagon concentration in presence and absence of co-administered itraconazole or rifampicin 10-12 days
- Secondary Outcome Measures
Name Time Method Maximum observed plasma concentration (Cmax) 10-12 days Number and type of adverse events 12-14 days Change from baseline in 12-lead ECG 12-14 days Change from baseline in vital signs and physical examination 12-14 days Change from baseline in laboratory assessments 12-14 days Area under the plasma concentration curve versus time curve with extrapolation to infinity (AUC(0-infinity)) 10-12 days
Trial Locations
- Locations (1)
PAREXEL Early Phase Clinical Unit Berlin
🇩🇪Berlin, Germany