USA-based drugmaker Biogen Idec and Swiss biotechnology company mondoBiotech AG say they have signed an exclusive license and collaboration agreement which covers the development and manufacture of Aviptadil (vasoactive intestinal peptide) as a treatment for pulmonary arterial hypertension.
Aviptadil, which has received Orphan Drug designation for PAH in the USA and Europe, and has already demonstrated its efficacy in a Phase II trial, where it brought about an improvement in physical exercise capacity after three to six months of treatment.
Under the terms of the deal, mondoBiotech is entitled to receive a $7.5 million upfront fee and up to $30.0 million in milestone payments, based on the successful commercialization of the drug in the USA and Europe. The Swiss firm will also be entitled to royalties based on sales. In return, Biogen will take responsibility for all clinical development and manufacturing, and has said that it will finalize its development plan for the product and initiate more clinical work in 2007.
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