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Study identifier: NCT06202001 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Irinotecan, TAS-102 Plus Bevacizumab as a Second-Line Therapy in mCRC Patients

Condition: Metastatic Colorectal Cancer  ·  Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences

PhasePhase 1/Phase 2
Planned participants70
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

In mCRC, response to second-line chemotherapy is limited, and few treatment options are available. It is urgent to design an optimal second-line treatment regimen to improve the response rate and prolong the survival of patients with mCRC. Several studies preliminarily demonstrated that irinotecan, TAS-102 plus bevacizumab regimen could bring promising efficacy with a tolerable safety profile for patients with mCRC as a second-line treatment. This phase I/II study was aimed to determine the recommended phase II dose (RP2D) of the combination of TAS-102, irinotecan, and bevacizumab for future clinical trials in patients with mCRC refractory to both fluoropyrimidine and oxaliplatin and to evaluate its safety and preliminary efficacy.

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

Talk to the study team

Yongkun Sun  ·  +8613141276041  ·  hsunyk@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

Cancer Hospital, Chinese Academy of Medical SciencesBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06202001