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Bioequivalence Study of Two Irbesartan in Healthy Chinese Subjects

Therapeutic Equivalency Clinical Trial

Official title:
Bioequivalence Study of Two Irbesartan in Healthy Chinese Subjects: an Open, Randomized, Single-Dose and Crossover Study

Clinical Trial Summary

The bioavailability of Irbesartan (150 mg) developed by Shenzhen Haibin Pharmaceutical Co., Ltd. was compared with that of reference Irbesartan (Aprovel ®,150 mg) produced by Sanofi Clir SNC. The bioequivalence of single dose of test preparation and reference preparation was evaluated in heathy subjects under fasting and fed conditions.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05786339
Study type Interventional
Source The Affiliated Hospital of Qingdao University
Contact
Status Completed
Phase Phase 1
Start date November 17, 2018
Completion date May 15, 2019
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