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中文(ZH) 复星医药:控股子公司药品DM1001制剂获临床试验批准

Fosun Pharma subsidiary gets nod for Parkinson's drug trial

Fosun Pharmaceutical has announced that its subsidiary, Fosun Wanbang, has received approval from the National Medical Products Administration to conduct clinical trials for DM1001, a treatment for idiopathic Parkinson's disease in adults. The Phase I clinical trial is planned to commence in China once conditions are met. Separately, China has placed 14 EU entities, including Lafayette Group, on an export control list, prohibiting the transfer of dual-use items to them to safeguard national security and international obligations. AI

RANK_REASON This item reports on a subsidiary receiving approval for clinical trials of a drug, which falls under product development but is not a frontier release from a major AI lab.

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Fosun Pharma subsidiary gets nod for Parkinson's drug trial

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  1. 36氪 (36Kr) TIER_1 中文(ZH) ·

    Fosun Pharma: Subsidiary's Drug DM1001 Formulation Approved for Clinical Trial

    36氪获悉,复星医药公告,近日,公司控股子公司复星万邦(江苏)医药集团有限公司(简称“复星万邦”)收到国家药监局关于同意DM1001制剂用于治疗成人特发性帕金森病的体征和症状开展临床试验的批准。复星万邦拟于条件具备后于中国境内开展该药品的I期临床试验。