8月5日（路透社）——NewAmsterdam Pharma公司N.V.今日宣布，其两款药物Obicetrapib及Obicetrapib/依折麦布（Obicetrapib/Ezetimibe）已获得欧洲药品管理局（EMA）人用药品委员会（CHMP）的积极意见。这一里程碑式的进展，标志着该公司的研发管线迈出了关键一步。
此外，公司透露，PREVAIL研究的中期分析计划于2026年第四季度进行，预计相关结果将在2027年第一季度公布。与此同时，RUBENS三期临床试验的顶线数据有望在2026年年底前出炉。这一连串的预期时间点，为投资者勾勒出清晰的研发进展路线图。
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