Trials / Completed
CompletedNCT01511731
Bioavailability Study of Famotidine Tablets 40 mg Under Fasting Conditions
Open-label, Randomized, 2-way Crossover Study to Compare the Bioavailability of Reddy Cheminor and Merck &Co, Pepcid Famotidine Tablets 40 mg Under Fasting Conditions.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Dr. Reddy's Laboratories Limited · Industry
- Sex
- Male
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was to compare the single-dose relative bioavailability of Reddy Cheminor and Merck \&Co, pepcid 40 mg famotidine tablets under fasting conditions.
Detailed description
Detailed Description : The study was conducted as an open-label, randomized, single-dose, 2-way crossover, relative bioavailability study performed on 30 healthy adult male volunteers. A total of 30 subjects completed the clinical phase of the study. Single oral 40 mg doses were separated by a washout period of 7 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Famotidine | Famotidine Tablets 40 mg |
| DRUG | Pepcid | 40mg tablets |
Timeline
- Start date
- 1998-10-01
- Primary completion
- 1998-10-01
- Completion
- 1998-10-01
- First posted
- 2012-01-19
- Last updated
- 2012-01-19
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01511731. Inclusion in this directory is not an endorsement.