Sales of US drugmaker Vivus' (Nasdaq: VVUS) obesity agent Qsymia (phentermine and topiramate extended-release) rose 432% sequentially in its second week post launch, according to Healthcare Analytics (formerly Wolters Kluwer) data reported by Credit Suisse.
While it often takes several weeks for data to reflect true demand, payers and patients appear to be adopting Qsymia, the first obesity agent in more than a decade, note analysts at Credit Suisse. Arena and Eisai's Belviq (lorcaserin), which was approved by the US food and Drug Administration ahead of Qsymia (The Pharma Letter June 28), could launch in the fourth quarter of this year. A delay in the launch of Belviq is due to the fact that the FDA has recommended that the drug be classified by the US Drug Enforcement Administration (DEA) as a scheduled drug.
Credit Suisse analysts have a net present value for Qsymia of $30.63 per share, 82% of the total for Vivus.
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