Clinical Trials Directory

Trials / Completed

CompletedNCT01577914

Bioequivalence Study of Carvedilol Tablets USP 12.5 mg Under Fasting Condition

A Randomized, Open Label, Balanced, Two-Treatment, Two-Period, Two-Sequence, Single Dose, Crossover, Bioequivalence Study of Carvedilol Tablets USP 12.5 mg With Coreg® 12.5 mg in Normal, Healthy, Adult, Human Subjects Under Fasting Condition.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
42 (actual)
Sponsor
IPCA Laboratories Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This is a randomized, open Label, balanced, two-treatment, two-period, two-sequence, single dose, cross over pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fasting condition in normal, healthy, adult, human subjects.

Detailed description

Objective of this pivotal study was to assess the bioequivalence between Test Product: Carvedilol Tablets USP 12.5 mg of M/s Ipca Laboratories Limited, India and the corresponding Reference Product: Coreg® (Carvedilol Tablets) 12.5 mg Tablets of M/s GlaxoSmithKline, under fasting condition in normal, healthy, adult, human subjects in a randomized crossover study. The study was conducted with 42 healthy adult subjects. In each study period, a single 12.5 mg dose of either test or reference was administered to the subjects as per the randomization schedule in each study period with about 240 mL of water at ambient temperature in sitting position. The duration of the clinical phase was approximately 11 days including washout period of at least 7 days between administrations of study drug in each study period.

Conditions

Interventions

TypeNameDescription
DRUGCarvedilol Tablets USP 12.5 mg12.5mg tablet once a day
DRUGCarvedilol12.5mg tablet once a day

Timeline

Start date
2011-07-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2012-04-16
Last updated
2012-07-09

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01577914. Inclusion in this directory is not an endorsement.