Clinical Trials Directory

Trials / Completed

CompletedNCT00649324

Fasting Study of Hydrochlorothiazide Tablets 50 mg to Hydrochlorothiazide Tablets 50 mg

Single-Dose Fasting In-Vivo Bioequivalence Study of Hydrochlorothiazide Tablets (50 mg; Mylan) to Hydrochlorothiazide Tablets (50 mg; Ivax) in Healthy Volunteers

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Mylan Pharmaceuticals Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to investigate the bioequivalence of Mylan's hydrochlorothiazide 50 mg tablets to Ivax's Hydrochlorothiazide 50 mg tablets following a single, oral 50 mg (1 x 50 mg) dose administered under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGHydrochlorothiazide Tablets 50 mg50mg, single dose fasting
DRUGHydrochlorothiazide Tablets (50 mg50mg, single dose fasting

Timeline

Start date
2005-10-01
Primary completion
2005-10-01
Completion
2005-10-01
First posted
2008-04-01
Last updated
2024-04-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00649324. Inclusion in this directory is not an endorsement.