信达生物IBI3033启动I期临床适应症为哮喘、特应性皮炎

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药物临床试验登记与信息公示平台数据显示，信达生物制药（苏州）有限公司的一项评估IBI3033在健康受试者中安全性、耐受性及药代动力学的随机、双盲、安慰剂对照、单次给药剂量递增研究已启动。临床试验登记号为CTR20255057，首次公示信息日期为2025年12月18日。该药物剂型为注射液（西林瓶），用法用量按照临床方案给药，用药时程为单次给药。本次试验目的为评估中国健康受试者接受IBI3033单次...

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信达生物IBI3033启动I期临床 适应症为哮喘、特应性皮炎

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信达生物IBI3033启动I期临床适应症为哮喘、特应性皮炎