Status:
COMPLETED
Bioequivalence Study of FLURBIPROFEN 100 mg FAMOTIDINE 20 mg MULTI-LAYER TABLET in Healthy Subjects Under Fasting Conditions
Lead Sponsor:
Pharmaceutical Research Unit, Jordan
Conditions:
Healthy
Eligibility:
MALE
18-45 years
Phase:
PHASE1
Brief Summary
To assess the bioequivalence of Test oral formulation of FLURBIPROFEN 100 mg FAMOTIDINE 20 mg MULTI-LAYER TABLET versus Reference ANTADYS®100 mg Comprimé Pelliculé \& PEPCID® (Famotidine) 20mg Tablets...
Detailed Description
An open-label, randomized, single dose, two-treatment, two-period, two-sequence, crossover bioequivalence with a washout period of at least 7 days between doses Healthy mixed skin Arab \& Mediterranea...
Eligibility Criteria
Inclusion
- Healthy Male subjects.
- Ethnic Group: Arab \& Mediterranean
- Race: Mixed skin (white \& black skin people).
- Age 18-45 years
- Body-mass index 18.5 to 30.0 kg/m2 inclusive
- Subject is available for the whole study period and gave written informed consent
- Physical examination within normal ranges
- All laboratory screening results within the normal range, or being assessed as clinically non-significant by the attending physician.
- Vital signs within normal ranges (Unless clinical investigator classified as insignificant).
- Normal Kidney \& Liver function tests (Unless clinical investigator classified as insignificant).
- Normal Cardiovascular system.
- Normal Digestive system.
Exclusion
- Women.
- Ethnic Group (Non- Arab \&/ or Non- Mediterranean)
- History of severe allergy or allergic reactions to study drug or related drugs
- Known history or presence of food allergies, or any condition known to interfere with the absorption, distribution, metabolism or excretion of drugs
- History of serious illness that can impact fate of drugs
- Known history or presence of cardiac, pulmonary, gastrointestinal, endocrine, musculoskeletal, neurological, hematological, liver or kidney disease, unless judged not clinically significant by the Principal Investigator, or medical designate
- Clinically significant illness 4 weeks before study Period I
- Mental disease, drug, alcohol, solvents or caffeine abuse, smoking.
- Regular use of medication
- Having taken medication that could affect the investigated drug product: a) Regular consumption of drugs during the two weeks prior to study initiation day, b) consumption of enzyme stimulating or inhibiting drugs (e.g. Barbiturates, Carbamazepine, Phenytoin) during one month before the study initiation.
- Presence of any significant physical or organ abnormality
- Donation of 1) at least 400 ml of blood within 60 days, or 2) more than 150 ml of blood within 30 days, or 3) more than 100 ml blood plasma or platelets within 14 days before study Period I
- Participation in another bioequivalence study within 80 days prior to the start of this study Period I
- Following a special diet (e.g. vegetarian) or dieting one month before the study initiation.
- History of Gastrointestinal diseases
- Prior history of hypersensitivity to Flurbiprofen or Famotidine and other competitive inhibitor of histamine H2-receptors.
- Consumption of grapefruit or grapefruit containing products within 7 days of drug administration
- Ingestion of any vitamins or herbal products within 7 days prior to the initial dose of the study medication.
- Exhausting physical exercise in the last 48 hours (e.g. weight lifting) or any recent significant change in dietary or exercise habits.
- Any significant clinical abnormality including HBsAg, HCV, and HIV
- Abnormal vital signs
- Abnormal Kidney or Liver function tests.
- Abnormal Cardiovascular system.
- Abnormal Digestive system
- Vomiting, Diarrhea.
Key Trial Info
Start Date :
December 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2013
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT01910090
Start Date
December 1 2012
End Date
January 1 2013
Last Update
July 29 2013
Active Locations (1)
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1
Arab Pharmaceutical industry Consulting/ Pharmaceutical Research Unit
Amman, Jordan, 00962