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优先审评资格的授予是基于名为ClarIDHy的3期临床试验数据。新闻稿指出,该研究是首个针对携带IDH1突变的经治胆管癌患者的随机3期临床试验。
参考资料:
[1] Servier Announces FDA Filing Acceptance and Priority Review for TIBSOVO® (ivosidenib tablets) in IDH1-mutated Cholangiocarcinoma. Retrieved May 5, 2021, from https://www.prnewswire.com/news-releases/servier-announces-fda-filing-acceptance-and-priority-review-for-tibsovo-ivosidenib-tablets-in-idh1-mutated-cholangiocarcinoma-301283821.html
[2] Agios Presents Final Data from Phase 3 ClarIDHy Study of TIBSOVO® (ivosidenib tablets) in Patients with Previously Treated IDH1-Mutant Cholangiocarcinoma. Retrieved January, 17, 2021, from https://investor.agios.com/news-releases/news-release-details/agios-presents-final-data-phase-3-claridhy-study-tibsovor
[3] Data from Agios’ Phase 3 ClarIDHy Trial of TIBSOVO® Demonstrates Significant Improvement in Progression Free Survival (PFS) Compared to Placebo in Previously Treated IDH1 Mutant Cholangiocarcinoma Patients. Retrieved September 30, 2019, from https://investor.agios.com/news-releases/news-release-details/data-agios-phase-3-claridhy-trial-tibsovor-demonstrates
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