歌禮制藥ASC50治療銀屑病新藥臨牀試驗申請已獲FDA批准

財中社

05-22

　　5月22日，歌禮制藥-B（01672）發佈公告，宣佈其自主研發的口服小分子IL-17抑制劑ASC50治療銀屑病的新藥臨牀試驗申請已獲得美國FDA批准。ASC50在臨牀前研究中顯示出比當前臨牀開發階段的其他口服小分子IL-17抑制劑更高的藥物暴露量、更長的半衰期以及更低的清除率，表明其有望成爲同類最佳的口服藥物。

（文章來源：財中社）

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