World drug giant Pfizer has terminated Phase III development programs for the investigational drugs esreboxetine for fibromyalgia and PD 332,334 for generalized anxiety disorder. After reviewing the results of the first late-stage trial for PD 332,334 and the existing data for esreboxetine, along with current market dynamics, it decided it was considered unlikely that either compound would provide meaningful benefit to patients beyond the current standard-of-care. Neither product was terminated due to safety reasons, Pfizer stressed. Pedro Lichtinger, president and general manager of Pfizer's primary care business unit, said: "we continually review our portfolio to ensure we are developing medicines in areas of unmet need and have found significant potential opportunities to bring more value to patients and our company." New York-based Pfizer is struggling to bolster its pipeline ahead of the November 2011 expiration of the patent on its best selling product, the $13.0-billion-a-year cholesterol drug Lipitor (atorvastatin).
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