USA-based CV Therapeutics says that the Food and Drug Administration has approved a new, first-line indication for Ranexa (ranolazine extended-release tablets) for the treatment of chronic angina.
The new labeling also provides information showing that the agent reduced arrhythmias including ventricular arrhythmias, new-onset atrial fibrillation and bradycardia in patients with coronary artery disease. In addition, it states that Ranexa reduces HbA1c in patients with diabetes.
According to the revised packaging information, Ranexa is indicated for the treatment of chronic angina and may be used alone or in combination with traditional therapies, such as beta blockers, calcium channel blockers and nitrates, as well as common cardio-protective treatments for cardiovascular disease such as anti-platelet therapy, lipid-lowering therapy, angiotensin-converting enzyme inhibitor and angiotensin receptor blockers.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Sign up to receive email updates
Join industry leaders for a daily roundup of biotech & pharma news
| Headless Content Management with Blaze