Test if a combined treatment with bilastine and montelukast can improve rhinoconjuctivitis and asthma symptoms
- Conditions
- Seasonal allergic rhinoconjunctivitis and asthmaTherapeutic area: Body processes [G] - Immune system processes [G12]
- Registration Number
- EUCTR2015-004806-40-SK
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 420
1) Patients aged 18 years or older;
2) Patients with at least 2 years history of SARC prior to the study and mild to moderate asthma (GINA criteria 2 and 3) inadequately controlled on inhaled corticosteroids and in whom as-needed” short acting beta-agonists provide inadequate clinical control;
3) FEV1 > 70% of the predicted normal value demonstrable at least 6 hours after last short acting ß-2 agonist use or 12 hours after last long acting ß-2 agonist use;
4) NSS at baseline = 3. Baseline NSS will be defined as the mean of the 6 last assessments of the patients’ diary (3 last days before randomization);
5) Positive results of skin prick test on at least one seasonal allergen within the last 3 years;
6) Patients who provided a signed written informed consent form;
7) Patients who are able and willing to complete web-based Patient’s Diary;
8) Patients who agree to maintain consistency in their surroundings throughout the study period;
9) Women of childbearing potential (WOCBP) including peri-menopausal women who have had a menstrual period within 1 year had to have a negative pregnancy test. Results had to be available on the Visit 2 and negative for the patient to be entered in the study.
10) WOCBP have to use an effective method of birth control throughout the study period and for 4 weeks after study completion (defined as a method which results in a failure rate of less than 1% per year) such as:
• combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal)
• progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable)
• intrauterine device (IUD)
• intrauterine hormone-releasing system (IUS)
• bilateral tubal occlusion
• vasectomised partner (provided that partner is the sole sexual partner of the trial participant and that the vasectomised partner has received medical assessment of the surgical success)
• sexual abstinence
In each case of delayed menstrual period (over one month between menstruations) confirmation of absence of pregnancy is strongly recommended. This recommendation also applies to WOCBP with infrequent or irregular menstrual cycles.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 454
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
1) Patients with hypersensitivity to any component of the study medications;
2) Patients with non-allergic rhinoconjunctivtis (e.g. vasomotor, infectious, drug-induced);
3) Presence of nasal polyps or any clinically important nasal anomaly;
4) History of acute and/or chronic sinusitis within 30 days of Visit 2;
5) History of eye surgery within 3 months of Visit 2;
6) History of intranasal surgery within 3 months of Visit 2;
7) Immunotherapy within 6 months prior to Visit 2;
8) Upper respiratory infections including cold and systemic infections within 3 weeks of Visit 2;
9) Patients with moderate to severe renal impairment and taking P-gp inhibitors (e.g. ketoconazole, erythromycin, cyclosporine, ritonavir, diltiazem) within 7 days from the first dose of study medication;
10) Patients requiring daily controller” medications with cromolyn-type drugs or leukotriene antagonists;
11) Patient required daily controller” medication with ICS or LABA/ICS at medium /high dosage (as defined in GINA table attached);
12) Patients with clinically important (based on principal investigator’s judgment) hepatic impairment;
13) Patients with severe concomitant disease (based on principal investigator’s judgment) that could interfere with treatment response;
14) Patients with QT syndrome;
15) Patients with Galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption;
16) Pregnant or breast-feeding women;
17) Patients with a mental condition rendering the subject unable to understand the nature, scope and possible consequences of the study (based on principal investigator’s judgment);
18) Patients who had a recent history (within previous 12 months) of drug addiction or alcohol abuse based on Principal investigator’s judgment;
19) Patients participating in or having participated in another clinical trial within the previous three months;
20) Patients unable to take relief medications due to contraindications or intolerance;
21) Patients who are taking or have taken any of the following medications prior to randomisation in the study and have not complied with the specified washout period:
Antihistaminic drugs or montelukast (7 days)
Systemic or intranasal corticosteroids (4 weeks)
Delayed-release corticosteroids (3 months)
Ketotifen (2 weeks)
Macrolides antibiotics and imidazolic antifungals (systemic)(7 days)
Anticholinergics (7 days)
Drugs with antihistamine properties (phenothiazine) (7 days)
Intranasal and systemic decongestants (3 days)
Lodoxamide (7 days)
22) Patients who will be operating heavy machinery or need to drive motor vehicles as an essential part of their profession.
23) Patients who are planning to travel outside the study area during the course of the study.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method