Clinical Trials Directory

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

TypeNameDescription
DRUGFamotidineFamotidine Tablets 40 mg
DRUGPepcid40mg 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.

Bioavailability Study of Famotidine Tablets 40 mg Under Fasting Conditions (NCT01511731) · Clinical Trials Directory