RecruitingHypertension (HTN)

An Open-label Extension Safety and Efficacy Study of QCZ484 in Hypertensive Patients.

Eligible age

18+ yrs

Accepts

All genders

Locations

13 states

Healthy volunteers

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About this study

The purpose of this extension study is to collect additional safety and efficacy on QCZ484 for hypertensive patients who successfully completed the parent study, CQCZ484A12201 or additional QCZ484 studies as specified in the respective parent study protocols.

Sponsor: Novartis Pharmaceuticals

You may qualify if…

✓ 1. Signed informed consent must be obtained prior to participation in the study.
✓ 2. Successful completion of treatment period on QCZ484 study medication in parent study.
✓ 3. No significant safety issue that may place participant at safety risk as determined by the Investigator.

You may not qualify if…

✕ Participants meeting any of the following criteria, may it be pre-existing or developed during the parent study, are not eligible for inclusion in this study:
✕ 1. Evidence of hepatic disease that would put participant at risk by taking QCZ484 for long term as determined by the Investigator.
✕ 2. Clinically significant cardiac arrhythmias (e.g., ventricular tachycardia), high-grade atrioventricular (AV) block (e.g., Mobitz type II and third-degree AV block in absence of a pacemaker) developed during the parent study.
✕ 3. Permanent or persistent atrial fibrillation developed during the parent study.
✕ 4. Clinically significant valvular heart disease developed during the parent study.
✕ 5. Acute myocardial infarction (AMI) or unstable angina, or any percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG) developed during the parent study. Any history of ischemic or hemorrhagic stroke or transient ischemic attack any time prior to enrollment.
✕ Other protocol-defined inclusion/exclusion criteria may apply