Clinical Trials Directory

Trials / Completed

CompletedNCT01603186

Bioequivalence Study of Quetiapine Fumarate Tablets 25 mg Under Fed Condition

A Randomized, Open Label, Two-Treatment, Two-Period, Two-Sequence, Crossover, Single Dose, Bioequivalence Study of Quetiapine Fumarate Tablets 25 mg With Seroquel® 25 mg in Normal, Healthy, Adult, Human Subjects, Under Fed Condition

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

Summary

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

Detailed description

Objective of this pivotal study was to assess the bioequivalence between Test Product: Quetiapine Fumarate Tablets 25 mg of M/s Ipca Laboratories Limited, India and the corresponding Reference Product: Seroquel® (Quetiapine fumarate) Tablets 25 mg of M/s AstraZeneca Pharmaceuticals LP, USA, under fed condition in normal, healthy, adult, human subjects in a randomized crossover study. The study was conducted with 54 healthy adult subjects. In each study period, a single 25 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
DRUGQuetiapine Fumarate Tablets 25 mg25 mg tablet once a day
DRUGQuetiapine Fumarate25 mg tablet once a day

Timeline

Start date
2011-04-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2012-05-22
Last updated
2012-07-09

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01603186. Inclusion in this directory is not an endorsement.