Bioequivalence Study Of Verapamil

NCT00668967 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2009-07-08

No results posted yet for this study

Summary

The purpose of this study is to demonstrate bioequivalence of single doses of two verapamil formulations

Conditions

  • Healthy Volunteers

Interventions

DRUG

verapamil

240 mg extended release tablets once daily at bedtime for 28 days

DRUG

verapamil

240 mg extended release tablets once daily at bedtime for 28 days

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-02-29
Primary Completion
2008-07-31
Completion
2008-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00668967 on ClinicalTrials.gov