Biopharmaceutical firm Biovitrum, listed on the Stockholm, Sweden, Stock Exchange since September 15, has entered an agreement with the Uppsala-based biotechnology company Resistentia Pharmaceuticals AB for process development and manufacturing of the substance RES 08, intended for use in Phase III clinical trials of the latter's new protein-based drug candidate for the treatment of allergy.
With the onset of an allergic reaction, allergy antibodies (IgE, immunoglobulin E, a specific protein in our immune system) are formed against a specific substance, for example pollen, dust, etc. Resistentia has developed a protein-based drug candidate that blocks the effect of IgE preventing an allergic reaction. RES 08 is a recombinant fusion protein (a protein with a compound structure produced by biotechnical methods) that initially is intended for the treatment of IgE-mediated allergies.
Biovitrum's assignment is to develop the existing process for the biotechnical manufacturing of RES 08 to a standard that meets the high demands of a Phase III trial, and furthermore to manufacture sufficient amounts of the substance for the study. The project will run for more than two years, beginning this month.
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