众生药业：RAY1225注射液获FDA批准在美国开展II期临床研究

证券之星08-17

证券之星消息，众生药业(002317)08月17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：请问1225是否已经启动美国的二期临床，目前进展如何？谢谢

众生药业回复：您好！公司的RAY1225注射液已获得FDA批准在美国开展超重或肥胖患者的II期临床研究。公司积极寻求国际合作，组织开展国际多中心临床研究，争取早日完成相关研究，申报药物上市，为广大患者提供更多治疗选择。谢谢！

本文数据来源于深圳证券交易所互动易，仅供参考不构成投资建议。

责任编辑：陈思雨

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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