一周内，3款国产新药临床试验申请已获FDA批准

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近年来中国医药产业加速向“全球创新”转型，国产创新药密集申请FDA临床，一周内3款国产新药临床试验申请获FDA批准。中国生物制药TQF3250胶囊获中美批准，拟用于减重，治疗2型糖尿病申请也获NMPA批准，其有望实现更优血糖与体重控制；石药集团SYH2056片获FDA批准在美国开展临床试验，该药为选择性5-HT2A受体激动剂，用于治疗抑郁症，单次给药快速起效且无致幻风险；和誉药业ABSK141获...

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