Fosun Pharma (02196) has announced that its subsidiary, Fosun Wanbang (Jiangsu) Pharmaceutical Group Co., Ltd., has received approval from the National Medical Products Administration to conduct clinical trials for the DM1001 formulation. This medication is intended for the treatment of signs and symptoms of idiopathic Parkinson's disease in adults.
Fosun Wanbang plans to initiate Phase I clinical trials of the drug in China once conditions are met. The drug is classified as a chemical pharmaceutical.
As of June 2026, the cumulative research and development investment by the Group in this drug amounts to approximately RMB 6.95 million, inclusive of licensing fees and unaudited. According to the latest IQVIA CHPA data, sales of the same compound drug in China were approximately RMB 375 million in 2025.
This article is based on information from Sina Finance.
Comments