Status:
COMPLETED
Bioequivalence Study Between Two Oral Formulations of Famotidine Tablets Under Fed Conditions
Lead Sponsor:
Perrigo Company
Conditions:
Bioavailability
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
Compare the rate and extent of absorption of famotidine 40 mg tablets, administered as 1 x 40 mg tablet under fed conditions.
Eligibility Criteria
Inclusion
- healthy men or women 18 years of age or older
- body mass index below 30.0 kg/m2
- willing to participate and sin a copy of the informed consent form
Exclusion
- recent history of drug or alcohol addiction or abuse
- pregnant or lactating women
- history of allergic response to heparin, famotidine, other H2-receptor antagonists, or other related drugs
- evidence of a clinically significant disorder or whose laboratory results were deemed to be clinically significant
- smoking more than 25 cigarettes per day
Key Trial Info
Start Date :
June 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT00803192
Start Date
June 1 2004
Last Update
March 16 2012
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