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Study identifier: NCT06685276 Synced from ClinicalTrials.gov · July 28, 2026
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Safety and Efficacy of Fruquintinib Plus Chidamide and Sintilimab in the Third and Later Line Treatment of MSS/pMMR Metastatic Colorectal Cancer

Condition: Colorectal Cancer Metastatic  ·  Sponsor: Dai, Guanghai

PhasePhase 2
Planned participants46
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The prognosis of most patients with unresectable locally advanced or metastatic colorectal cancer (CRC) remains poor despite the advancements in chemotherapy and target therapy. CAPability-01 trial investigated the potential efficacy of combining the programmed cell death protein-1 (PD-1) monoclonal antibody sintilimab with the histone deacetylase inhibitor (HDACi) chidamide with or without the anti-vascular endothelial growth factor (VEGF) monoclonal antibody bevacizumab in patients with unresectable chemotherapy-refractory locally advanced or metastatic microsatellite stable/proficient mismatch repair (MSS/pMMR) colorectal cancer. Based on the previous findings of CAPability-01, we will further evaluate the efficacy and safety of sintilimab and chidamide in combination with fruquintinib in the same setting.

This description comes directly from the study's public registry record.

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Locations (1)

China PLAGHBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06685276