RecruitingPhase 2NCT07728019

Efficacy and Safety of Retlirafusp Alfa Plus Bevacizumab and Chemotherapy With or Without Short-Course Radiotherapy in Patients With CRCLM

Efficacy and Safety of Retlirafusp Alfa Plus Bevacizumab and Chemotherapy With or Without Short-Course Radiotherapy in Patients With Colorectal Cancer Liver Metastases: a Randomized Phase II Study


Sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Enrollment

60 participants

Start Date

Jul 30, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Efficacy and safety of retlirafusp alfa combined with bevacizumab and chemotherapy with or without short-course radiotherapy in conversion therapy for advanced colorectal cancer liver metastases: an exploratory study.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Bevacizumab, a drug called CAPOX, and others for people with crc (colorectal cancer). The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 75 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONSCRT

short-course radiotherapy

DRUGRetlirafusp alfa Injection

Retlirafusp alfa :1800 mg via intravenous infusion every 3 weeks (q3w)

DRUGBevacizumab

Bevacizumab: 7.5 mg/kg, D1, IV, Q3W

DRUGCAPOX

CAPOX:oxaliplatin 130 mg/m²,IV, D1 ; Capecitabine: 1000 mg/m² orally twice daily, Days 1-14; Cycle duration: 3 weeks per cycle


Locations(1)

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China

View Full Details on ClinicalTrials.gov

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NCT07728019


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