Samsung Bioepis Receives EU Marketing Authorization For Trastuzumab Biosimilar

Goodwin
Contact

Samsung Bioepis announced today that the European Commission (EC) has granted marketing authorization for Ontruzant®, a biosimilar for Herceptin® (trastuzumab), across all 28 European Union member states and the European Economic Area member states of Norway, Iceland and Liechtenstein. According to the press release, Ontruzuant® is approved for the treatment of early breast cancer, metastatic breast cancer and metastatic gastric cancer.  Samsung Bioepis stated that ONTRUZANT® will be commercialized by MSD, which is known as Merck in the United States and Canada.

Samsung Bioepis reports that this is its fourth biosimilar to receive EC marketing authorization, and the first trastuzumab biosimilar to receive regulatory approval in Europe.

DISCLAIMER: Because of the generality of this update, the information provided herein may not be applicable in all situations and should not be acted upon without specific legal advice based on particular situations.

© Goodwin | Attorney Advertising

Written by:

Goodwin
Contact
more
less

Goodwin on:

Reporters on Deadline

"My best business intelligence, in one easy email…"

Your first step to building a free, personalized, morning email brief covering pertinent authors and topics on JD Supra:
*By using the service, you signify your acceptance of JD Supra's Privacy Policy.
Custom Email Digest
- hide
- hide