Overview

VALORY Study of Valsartan/Hydrochlorizide for Patients Who do Not Respond Adequately to Olmesartan Medoxomil

Status:
Completed
Trial end date:
2005-04-01
Target enrollment:
Participant gender:
Summary
To evaluate the efficacy of valsartan 160 mg/HCTZ 25 mg in patients not adequately responding to monotherapy with olmesartan medoxomil 40 mg or combination therapy with olmesartan medoxomil 20 mg plus HCTZ 12.5 mg by testing the hypothesis that valsartan 160 mg/HCTZ 25 mg significantly reduces the trough mean sitting diastolic blood pressure (MSDBP) after a 4-week treatment in the nonresponder population.
Phase:
Phase 3
Details
Lead Sponsor:
Novartis
Treatments:
Hydrochlorothiazide
Olmesartan
Olmesartan Medoxomil
Valsartan