US emerging biotech firm Aegerion Pharmaceuticals (Nasdaq: AEGR) says that the Mexican Federal Commission for the Protection against Sanitary Risk (COFEPRIS) has approved Juxtapid (lomitapide).
The drug is an adjunct treatment to a low-fat diet and other lipid-lowering treatments, to reduce low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), apolipoprotein B (apo B) and non-high-density-lipoprotein cholesterol (non-HDL) in patients with homozygous familial hypercholesterolemia (HoFH). In the approval of Juxtapid, COFEPRIS gave Juxtapid recognition as an Orphan Drug.
Juxtapid has already been approved by the US Food and Drug Administration and by the European Commission; it is marketed under the trade name Lojuxta in Europe (The Pharma Letters December 12 and August 5, 2013).
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