生物制药公司Pulmovant今日宣布，其针对间质性肺病相关肺动脉高压（PH-ILD）研发的创新药物Mosliciguat，已顺利完成二期临床试验Phocus研究的全部患者招募工作。该里程碑标志着药物临床开发进入关键数据收集阶段，为后续疗效评估奠定基础。
本研究旨在评估Mosliciguat在PH-ILD患者中的安全性、耐受性及初步疗效。作为一款选择性可溶性鸟苷酸环化酶激动剂，该药物通过独特作用机制靶向肺动脉高压的病理生理过程。此次完成入组将加速临床试验进程，相关数据结果预计于2024年公布。
生物制药公司Pulmovant今日宣布，其针对间质性肺病相关肺动脉高压（PH-ILD）研发的创新药物Mosliciguat，已顺利完成二期临床试验Phocus研究的全部患者招募工作。该里程碑标志着药物临床开发进入关键数据收集阶段，为后续疗效评估奠定基础。
本研究旨在评估Mosliciguat在PH-ILD患者中的安全性、耐受性及初步疗效。作为一款选择性可溶性鸟苷酸环化酶激动剂，该药物通过独特作用机制靶向肺动脉高压的病理生理过程。此次完成入组将加速临床试验进程，相关数据结果预计于2024年公布。
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