Asthma, Bioequivalence
Conditions
Keywords
bioequivalence, asthma, fluticasone propionate, FLOVENT
Brief summary
Bioequivalence study between two inhaler products of ffluticasone propionate inhalation powder
Detailed description
A bioequivalence study of a single dose of Fluticasone Propionate 100 mcg/Blister Oral Inhalation Powder/Respirent Pharmaceuticals vs. FLOVENT DISKUS® 100 mcg/Blister Oral Inhalation Powder /GSK in Healthy Volunteers Under Fasting Conditions. The study will be one-center crossover, randomized, 2-period, 2-sequence (RT and TR), single dose, laboratory blinded.
Interventions
2 inhalations of Test and Reference product in each study period
DRUGFLOVENT DISKUS
2 inhalations of Test and Reference product in each study period
Sponsors
Becro Ltd.
Respirent Pharmaceuticals Co Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)
Masking description
Laboratory blinded
Intervention model description
One-center crossover, randomized, 2-period, 2-sequence (RT and TR), single dose, laboratory-blinded study
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy volunteers of both genders, aged ≥18 and ≤60 years. 2. Subjects with Body Mass Index (ΒΜΙ) ≥18.5 and \<30.0 kg/m2. 3. Healthy volunteers are declared healthy based on medical history, physical examination, ECG, pulmonary function test (a forced expiratory volume in 1 second (FEV1) \>=80% of the predicted normal value), and clinical laboratory values within the laboratory stated normal range; if not within this range, they must be without any clinical significance according to the Investigator. 4. Females who participate in the study are either unable to gestate \[i.e. post-menopausal (absence of menses for 12 months prior to drug administration), hysterectomy, bilateral oophorectomy, tubal ligation at least 6 months prior to drug administration\] or at reproductive age; Females of reproductive age if sexually active, must be practicing an effective method of birth control within 14 days prior to drug administration and throughout the study. Reliable contraception methods are considered the following: * combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation: oral, intravaginal or transdermal * progestogen-only hormonal contraception associated with inhibition of ovulation oral, implanable or injectable * intrauterine device (IUD) * intrauterine hormone-releasing system (IUS) * bilateral tubal occlusion * vasectomised partner * sexual abstinence 5. Subjects that are non-smokers. 6. Subjects that, in the opinion of the principal investigator/medical officer, are able to communicate and comply with the study procedures and protocol restrictions as evidenced by the Informed Consent Form (ICF) duly read, signed and dated by the subject prior to study initiation. 7. Subjects able to use the inhalers according to given instructions, as judged by the Investigator or study nurse.
Exclusion criteria
1. Hypersensitivity to the active substance(s) or to the excipient (lactose which contains small amounts of milk protein may cause allergic reactions) or related class (any sympathomimetic drug or any inhaled, intranasal, or systemic corticosteroid therapy) of the medicinal product 2. Clinically significant illness or surgery within four weeks prior to dosing. 3. Clinically significant ECG abnormalities or vital sign abnormalities (seated systolic blood pressure \<90 or \>140 mmHg, seated diastolic blood pressure \<50 or \>90 mmHg or heart rate less than 50 or over 100 bpm) at screening. 4. Clinically significant history or presence of chronic bronchitis, emphysema,asthma or any other lung disease. 5. History or presence of pulmonary tuberculosis. 6. Viral or bacterial, upper or lower respiratory tract infection or sinus or middle ear infection within 4 weeks prior to the screening visit. 7. History or presence of significant cardiovascular, endocrinal, neurologic, immunological, psychiatric or metabolic disease. 8. History of significant alcohol or drug abuse within one year prior to the screening visit. 9. Regular use of alcohol within six months prior to screening visit (more than 14 alcohol units per week) \[1Unit =150 ml of wine, 360 ml of beer, or 45 ml of 40% alcohol\]. 10. Inability to abstain from alcohol for the duration of study period. 11. Presence of disease markers for Hepatitis B, Hepatitis C or HIV at screening. 12. Positive results for drugs of abuse (barbiturates, marijuana, opioids, benzodiazepines and methadone) in saliva before each administration. 13. Positive alcohol breath test before each administration. 14. Use of soft drugs (such as marijuana) within three months prior to screening or hard drugs such as crack, cocaine or heroin within one year prior to screening visit 15. Intake of any drugs known to induce or inhibit hepatic drug metabolism (examples of inducers are barbiturates, carbamazepine, phenytoin, glucocorticoids, rifampin/rifabutin; examples of inhibitors are, erythromycin, ketoconazole, indinavir, cobicistat-containing products) within one month prior to administration of the study medication. Under these circumstances, subject inclusion will be judged by the principal investigator. 16. History of peptic ulcer, other gastrointestinal disorders (e.g. chronic diarrhoea, irritable bowel syndrome) or unresolved gastrointestinal symptoms (e.g. diarrhea, vomiting) or significant hepatic, renal or other condition that is known to interfere with the absorption, distribution, metabolism or excretion of the drug. 17. Use of oral or parenteral corticosteroids in the previous four 4 weeks 18. Eye disorders especially Glaucoma (or a family history of glaucoma) 19. Use of prescription medication (within 14 days prior to the first administration of study medication) or over-the-counter (OTC) products (including food supplements vitamins and herbal supplements) within one week (7 days) prior to the first administration of study medication, except for topical products without systematic absorption. Contraceptives are allowed. 20. Vaccination for prophylaxis from seasonal flu or any other vaccination within seven days prior to administration 21. History of allergy to any food, intolerance or special diet, that in the opinion of the medical sub-investigator could contraindicate the subject's participation in the study. 22. A depot injection or an implant of any drug (except hormonal contraceptives) within 3 months prior to treatment administration. 23. Donation of plasma (500 ml) within 7 days prior to treatment administration. 24. Donation of whole blood or loss of whole blood ≥ 500 ml prior to administration of the study medication within 30 days prior to treatment administration. 25. Participation in another clinical trial simultaneously. 26. Subjects receiving special diet or having intolerance in any of the provided study meals or refusing to eat the study meals 27. Application of tattoo or body piercing within 30 days prior to treatment administration. 28. Non-tolerance to venipuncture. 29. Breastfeeding women. 30. Positive pregnancy test at screening
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cmax | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Maximum plasma concentration, it is read directly from the raw data |
| AUC(0-t) | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Area under the plasma concentration curve from time 0 to the last measured |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| t1/2 | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Plasma concentration halflife, it is calculated from the ratio 0.693/λZ |
| AUC0-∞ | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Area under the plasma concentration-time curve extrapolated to infinity |
| Residual Area | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | \[AUC(0-∞)-AUC(0-t)\]/AUC(0-∞)\] |
| λz | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Terminal elimination rate constant, calculated from the slope of the final phase of the ln-concentration curve versus time with regression analysis |
| Tmax | 3, 5, 10, 15, 30, 45 minutes, 1.00 hour, 1 hour and 20 minutes, 1 hour and 40 minutes, 2.00 hours, 2 hours and 30 minutes, 3.00, 4.00, 6.00, 8.00, 12.00, 14.00, 16.00, 24.00 and 36:00 hours post-administration | Time until Cmax is reached, it is read directly from the observed concentrations |
Countries
Greece
Contacts
Primary ContactChrysoula Kokkali, MSc
Backup ContactChrysoula Doxani, MD, MSc, Phd
Outcome results
None listed