Biosimilars pipeline
The Teva U.S. Biosimilars Pipeline provides an overview of biosimilar products approved, under regulatory review, or in development for the U.S. market. This page focuses specifically on biosimilar programs relevant to the United States and includes products developed in collaboration with partners such as Alvotech, mAbxience and Polpharma. For information about Teva's broader global portfolio of innovative medicines and biosimilars, please refer to the Global R&D Pipeline.
Explore Teva's Global R&D Pipeline to learn more about innovative medicines and biosimilar development worldwide.
Explore Teva's Global R&D Pipeline- Approved
- Under Regulatory Review
- Clinical
- Pre-Clinical
Approved
PONLIMSI®
(denosumab-adet)DEGEVMA®
(denosumab-adet)Under Regulatory Review
In collaboration with Alvotech for the U.S. Market
Biosimilar candidate to Xolair®
(omalizumab)In collaboration with Alvotech for the U.S. Market
Clinical
Pre-Clinical
Ocrevus® and Ocrevus Zunovo® are registered trademarks of Genentech, Inc. Simponi® and Simponi Aria® are registered trademarks of Johnson & Johnson. Eylea® is a registered trademark of Regeneron Pharmaceuticals, Inc. Xolair® is a registered trademark of Novartis AG. Entyvio® is a registered trademark of Millennium Pharmaceuticals, Inc.
FAQ
What does the U.S. Biosimilars Pipeline include?
This page provides an overview of Teva's biosimilar candidates that are approved, under regulatory review, or in development for the U.S. market. It focuses specifically on biosimilars and related development activities relevant to the United States.
How is this different from Teva's Global R&D Pipeline?
The Global R&D Pipeline includes Teva's broader portfolio of innovative medicines and biosimilars across all therapeutic areas and development stages worldwide. The U.S. Biosimilars Pipeline focuses specifically on biosimilar programs relevant to the U.S. market.