U.S. FDA approves biosimilar version of cancer drug Avastin
Sept 14 (Reuters) - The U.S. Food and Drug Administration said on Thursday it has approved Amgen Inc's (AMGN.O) biosimilar version of Roche Holding AG's (ROG.S) cancer drug Avastin.
Amgen's drug, Mvasi, was approved for multiple types of cancer and is the first biosimilar approved in the U.S. to treat cancer. Biosimilars are somewhat cheaper copies of biologic drugs.
Biologics are made from living cells and are therefore difficult to copy with precision. They are called biosimilars, not generics. Mvasi is approved to treat certain types of colorectal, lung, brain, kidney and cervical cancers.
Tel: +86 0871 6511 0906 (GMT+8 AM9:00-AM:12:00 PM1:30-PM6:00)
cell phone:188 1221 6310
Fax:0871-63602606
Email: info@luhancn.com
Address:Room 3301,33rd Floor Building B, Vogue Garden Plaza, No.1004 Beijing Road, Kunming, Yunnan Province, P. R. China 650000