Bioequivalence Study Between Two Oral Formulations of Gemfibrozil Tablets

NCT00800475 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2013-08-13

No results posted yet for this study

Summary

The purpose of this study is to determine whether two oral formulations of Gemfibrozil Tablets are bioequivalent.

Conditions

  • Bioavailability

Interventions

DRUG

Gemfibrozil Tablets

Sponsors & Collaborators

  • Blu Caribe

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2005-07-31
Completion
2005-09-30

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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 NCT00800475 on ClinicalTrials.gov