复星医药(600196.SH)子公司DM1001制剂获临床试验批准

智通财经07-24

智通财经APP讯，复星医药(600196.SH)发布公告，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”)收到国家药品监督管理局关于同意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。该药品系化学药物。根据IQVIA CHPA最新数据，2025年，相同化合物药品于中国境内的销售额约为3.75亿元。

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