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A Clinical Studyf of SHR-1701 or Placebo in Combination With BP102 and XELOX in the First-line Treatment of mCRC

NCT04856787 PHASE2, PHASE3 TERMINATED

This is a two-arm, randomized, double-blinded, multicenter phase II/III clinical study to evaluate the safety and clinical efficacy of SHR-1701 or placebo in combination with BP102 (biosimilar to bevacizumab) and XELOX in first-line treatment of patients with mCRC.

Details

Lead sponsorSuzhou Suncadia Biopharmaceuticals Co., Ltd.
PhasePHASE2, PHASE3
StatusTERMINATED
Enrolment62
Start dateTue Jun 22 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed Apr 17 2024 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

China