Lead asset and pipeline
Our lead asset serplulimab recently received a positive approval from CHMP of the EMA. Serplulimab is currently being evaluated for the treatment of ES-SCLC in a confirmatory bridging study in a US population. Serplulimab has been designated an orphan drug by the FDA and EC. Download information about serplulimab to learn more about:
Our clinical trials validate serplulimab as our lead asset for the treatment of ES-SCLC. ASTRUM-005 is a study with positive results that showed significant improvement compared to chemotherapy and had unprecedented mOS of 15.8 months. To achieve FDA approval, Fosun has initiated the ASTRIDE trial to confirm the results of ASTRUM-005 to patients with ES-SCLC in the United States.
Fosun Pharma USA has the ability to leverage the global operations footprint of our parent company to include R&D, manufacturing, and commercialization systems. Highlights of our capabilities include:
104 Carnegie Center, Suite 204
Princeton, NJ 08540
(609) 250-2802
info.usa@fosunpharma.com
Customer Service & Adverse Event/ Quality Concerns: (855) 282-4882 or fosuncs@eversana.com
© 2024 Fosun Pharma USA Inc. All rights reserved. | Privacy Notice