The European Commission has opened a formal antitrust investigation to assess whether an agreement between US-based pharmaceutical company Cephalon (Nasdaq: CEPH) and Israel-based generic drugs firm Teva Pharmaceutical Industries (Nasdaq: TEVA) may have had the object or effect of hindering the entry of generic modafinil (Cephalon’s Provigil brand) in the European Economic Area.
Modafinil is a medicine used for the treatment of certain types of sleeping disorders. The opening of proceedings does not mean that the Commission has conclusive proof of an infringement, only that it will investigate the case as a matter of priority.
The Commission has started an ex officio investigation to assess an agreement between Cephalon and Teva that may have the object or effect of hindering the entry of generic Modafinil products in the markets of the European Economic Area. In particular it is assessed whether the agreement is in breach of the European Union Treaty's rules on restrictive business practices (Article 101).
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