drugset / Trial / NCT00265967

Irbesartan in Hypertension

NCT00265967

Phase 4 Completed 88 enrolled Sanofi Bristol-Myers Squibb · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Study objectives: * To demonstrate the effect of irbesartan on the regulation of diastolic blood pressure, in case of missing one dose after a period of administration for 6 to 8 weeks * To evaluate the safety of irbesartan

Timeline

Start
2005-09
Primary completion
2007-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Irbesartan Small molecule 150 mg
Subject Irbesartan Small molecule 300 mg

Indications