French drug major Sanofi-Aventis says that its anti-obesity drug Acomplia (rimonabant), a selective cannabinoid-1 receptor antagonist, has now been included in the list of medicines that are reimbursable by France's Social Security system, although there are conditions.
In France, Acomplia's price has been set at 71.63 euros ($95.25), including tax, for a 28-day course, and will be reimbursable for obese patients (body-mass index equal to or greater than 30kg/m2) with type 2 diabetes uncontrolled by monotherapy with metformin or a sulphonurea and whose HbA1c is in the range of 6.5%-10%. However, to be entitled to the 35% Social Security reimbursement, the prescription must be issued on a special form (ordonnance de medicament d'exception) and conform to the details laid out in the Therapeutics Information Bulletin, the company explains.
Marketing approval for Acomplia was granted by the European Commission back in June 2006 and, in February this year, the French Ministry of Health's senior council of health recommended it should be made reimbursable (Marketletter February 12), but it is only now that it has been launched. However, with the restrictions of patients eligible, French sales of the product are not likely to be huge; the obese/diabetic patient population has been estimated at between 155,000 and 170,000.
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 2025 | Headless Content Management with Blaze