Efficacy and Safety of Valsartan and Amlodipine (± HCTZ) in Adults With Moderate, Inadequately Controlled Hypertension

• Status: Completed
• Trial end date: 2007-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will evaluate the efficacy and safety of valsartan and amlodipine in fixed dose combination in adults with moderate, inadequately controlled hypertension. There was an optional study extension for eligible patients who wanted to participate that contains the triple therapy (ie, hydrochlorothiazide+ amlodipine/valsartan).

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Novartis
• Treatments: Amlodipine; Amlodipine, Valsartan Drug Combination; Angiotensin Receptor Antagonists; Hydrochlorothiazide; Olmesartan; Olmesartan Medoxomil; Valsartan

Criteria

Inclusion Criteria for Core study:

• Male or female patients (>=18 years)

• Females must be either post-menopausal for one year, surgically sterile or using effective contraceptive methods

• Patients with essential hypertension (diastolic blood pressure >=100 mmHg and <110 mmHg)

Inclusion Criteria for Extension:

• Patients had to have a msSBP >= 140 mmHg and/or msDBP >= 90 mmHg at week 8 ie, end of core study.

Exclusion Criteria for Core study:

• Severe hypertension (diastolic blood pressure >=110 mmHg or systolic blood pressure >= 180 mmHg)

• Pregnant or nursing women

• Treated hypertensive patients with controlled hypertension under current therapy

• A history of cardiovascular disease, including angina pectoris, myocardial infarction, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, transient ischemic attack, stroke, and heart failure NYHA II - IV

Exclusion Criteria for Extension:

• prematurely discontinued the core study

• failed to comply with the core study protocol

Other protocol-defined inclusion/exclusion criteria applied to the study.