Biosimilars Approvals: Nepexto Receives European Marketing Authorization, Ziextenzo and Riximyo Receive Health Canada Approval

Goodwin
Contact

Goodwin

Last week, Lupin and Mylan announced that the European Commission had granted marketing authorization for their biosimilar Nepexto (etanercept) for all indications of the reference product.  The marketing authorization follows a positive opinion from the Committee for Medicinal Products for Human Use earlier this year based on preclinical and clinical studies demonstrating bioequivalence to the reference product, Enbrel.

Today, Sandoz Canada announced that Health Canada has approved the launch of Ziextenzo (pegfilgrastim), and Riximyo (rituximab) in Canada. According to the announcement, Sandoz Canada received a Notice of Compliance from Health Canada on April 21, 2020 for the use of Ziextenzo to reduce the incidence of febrile neutropenia, a decrease in while blood cells resulting from chemotherapy.  Likewise, Riximyo was approved on April 28, 2020 for the treatment of non-Hodgkin’s lymphoma, chronic lymphocytic leukemia and rheumatoid arthritis.

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