联邦制药(03933.HK)创新药UBT251注射液完成Ia期临床研究

阿斯达克财经08-13

联邦制药(03933.HK) 公布，公司自主研发的1类创新药UBT251注射液已完成在内地健康受试者的Ia期临床研究。结果显示，单次给药后各剂量组安全性和耐受性良好，无一例受试者退出，未发生严重不良事件，常见副反应为轻到中度的食欲减退和胃肠道相关不良事件。公司将快速推进 UBT251 注射液后续临床研究。(de/d)(港股报价延迟最少十五分钟。沽空资料截至 2024-08-12 16:25。)

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