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Crossover Bioequivalence Study of Irbesartan 300 mg Tablets Under Fed Conditions

2014-08-27 04:00:36 | BioPortfolio

Summary

The objective of this study was to prove the bioequivalence of Roxane Laboratories' Irbesartan 300 mg Tablets under fed conditions.

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Hypertension

Intervention

Irbesartan, Avapro

Location

Worldwide Clinical Trials Drug Development Solutions (formerly CEDRA Clinical Research)
San Antonio
Texas
United States
78217

Status

Completed

Source

Roxane Laboratories

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T04:00:36-0400

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