Clinical Trials Directory

Trials / Completed

CompletedNCT00647673

Fasting Study of Verapamil HCl Extended-Release Capsules 300 mg and Verelan® PM Extended-Release Capsules 300 mg

Single-Dose Fasting Bioequivalence Study of Verapamil HCl Extended-Release Capsules (300 mg; Mylan) to Verelan® PM Extended-Release Capsules (300 mg; Schwarz) in Healthy Volunteers Dosed in the Evening

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (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 verapamil HCl extended-release 300 mg capsules to Schwarz's Verelan® PM extended-release 300 mg capsules following evening administration of a single, oral 300 mg (1 x 300 mg) dose under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGVerapamil HCL Extended-Release Capsules 300 mg300mg, single dose fasting
DRUGVerelan® PM Extended-Release Capsules 300 mg300mg, single dose fasting

Timeline

Start date
2006-01-01
Primary completion
2006-01-01
Completion
2006-02-01
First posted
2008-04-01
Last updated
2024-04-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00647673. Inclusion in this directory is not an endorsement.