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Clinical Trial Summary

Phase 1b consists of combined dose escalation phase and dose expansion phase. Phase 3 study will compare efficacy and safety of IBI351 combined with cetuximab versus chemotherapy in treatment of KRAS G12C-mutated metastatic colorectal cancer


Clinical Trial Description

A Phase 1b study of the safety, tolerability and preliminary efficacy of IBI351 combined with cetuximab in the treatment of KRAS G12C mutant metastatic colorectal cancer will be conducted based on recommended dose of IBI351, which consists of combined dose escalation phase and dose expansion phase. After confirming the efficacy and safety of IBI351 combined with cetuximab in Phase Ib, an open-label Phase 3 study of the efficacy and safety of IBI351 combined with cetuximab versus oxaliplatin-based mFOLFOX6 regimen or irinotecan-based FOLFIRI with or without bevacizumab in treatment of KRAS G12C-mutated metastatic colorectal cancer will be conducted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05497336
Study type Interventional
Source Innovent Biologics (Suzhou) Co. Ltd.
Contact Chunxian Hu
Phone 0512-69566088
Email chunxian.hu@innoventbio.com
Status Recruiting
Phase Phase 1
Start date August 18, 2022
Completion date September 30, 2024

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