U.S. Approval of Biosimilar Cancer Drug Rocks Genentech
U.S. Approval of Biosimilar Cancer Drug Rocks Genentech
Attachment: Amergen
SUGAR LAND--September 18, 2017--Researched by Annette Kreuger, Industrial Info Resources (Sugar Land, Texas)--Biological drugmaker Genentech (a Roche company) (South San Francisco, California), the developer of the blockbuster cancer drug Avastin, was dealt a stunning blow on September 14 when the U.S. Food and Drug Administration (FDA) approved a biosimilar (generic biological drug). The biosimilar, Mvasi (bevacizumab-awwb), the result of a partnership between Amgen (AMGN) (Thousand Oaks, California) and Allergan (AGN) (Dublin, Ireland), was approved for certain colorectal, lung, brain, kidney and cervical cancers.
Subscribe Now!(All Fields Required)
Related Articles
Articles related to this company
- Pharma Company Zoetis Signs PPA with Scout Clean Energy to Support Growing ...
- China's Rongsheng Petrochemical Ups Role in Polyester Chips
- Suffolk Construction Has Hand in $1.9 Billion Worth of Projects
- U.S. Home to Billions' Worth of 2Q ESG Project Kickoffs
- Japan Hosts $832 Million in CDMO/CMO-Related Pharma Projects