复星医药子公司获美国FDA批准开展AGA治疗临床试验

财中社2025-05-09

5月9日，复星医药（600196/02196）发布公告，控股子公司菌济健康获得美国FDA关于LBP-ShC4开展临床试验的批准。该产品为公司自主研发的活体生物治疗产品，旨在治疗雄激素脱发（AGA）。截至2025年4月，公司在LBP-ShC4的研发上累计投入约为0.17亿元（未经审计）。公告指出，目前全球尚无用于治疗雄激素脱发的活体生物治疗产品获批上市。尽管获得临床试验批准，但药品研发存在风险，后续...

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