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Nuvation Bio,Nurai治疗非小细胞肺癌的申请已被EMA接受

2026-03-27 05:26

  • The European Medicines Agency has accepted a Marketing Authorisation Application filed by Nuvation Bio (NUVB) and Eisai (ESALF)(ESAIY) for taletrectinib to treat non-small cell lung cancer.
  • The application was given a standard review time of 210 "active" days. It is supported by data from two pivotal phase 2 studies, TRUST-I and TRUST-II.
  • Taletrectinib is already marketed as Ibtrozi in the US and Japan.

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