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迈威生物:9MW1911注射液获FDA临床试验许可_蜘蛛资讯网

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示与安慰剂相比,药物安全性和耐受性良好。  具体数据显示,在IIb期研究推荐剂量下,中重度COPD急性加重年化发生率较安慰剂组降低超30%,重度急性加重年化发生率较安慰剂组降低超40%。公司计划于2026年底启动III期临床研究,以进一步观察药物的安全性和有效性。  2025年前三季度,迈威生物实现收入5.66亿元,归母净利润-5.98亿元。(文章来源:财中社)

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