Adding extended-release (ER) niacin to statins does not reduce the chances of high risk patients having a heart attack or stroke, Oxford University scientists leading the HPS2-THRIVE study have revealed at the American College of Cardiology 62nd Annual Scientific (ACC) conference in San Francisco over the weekend.
HPS2-THRIVE was funded by a grant to Oxford University from Merck & Co (NYSE: MRK), which also provided the ER niacin/laropiprant (trade name Tredaprive) and matching placebo tablets, as well as background simvastatin or ezetimibe/simvastatin combination. However, the study was designed, conducted, analysed and interpreted independently by the investigators at Oxford University and the independent members of the study Steering Committee.
In addition, the researchers report that the use of ER niacin causes a significant number of different types of serious side effect. Some of these side effects were already known to be caused by niacin, but some of them were unexpected.
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze