贝达药业：统筹推进EYP-1901国内临床研究及上市申报

证券之星01-21

证券之星消息，贝达药业(300558)01月21日在投资者关系平台上答复投资者关心的问题。

投资者提问：为什么1901要等fda成功再引进国内，国内是有钱投仿制药也没钱做临床是吗？如果fda拒绝是不是1901就又没了？

贝达药业回复：您好！基于国外临床进展、国内商业化规划，公司将统筹推进EYP-1901的国内临床研究及上市申报工作。公司合作伙伴EYEPOINT公司已在2025年完成wAMD适应症的两项Ⅲ期临床入组，并计划在2026年一季度实现DME适应症的Ⅲ期临床的首例病人入组，相关临床工作正在顺利推进当中。谢谢！

以上内容为证券之星据公开信息整理，由AI算法生成（网信算备310104345710301240019号），不构成投资建议。

免责声明：本文观点仅代表作者个人观点，不构成本平台的投资建议，本平台不对文章信息准确性、完整性和及时性做出任何保证，亦不对因使用或信赖文章信息引发的任何损失承担责任。

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