RecruitingPhase 2NCT06455254

Cadonilimab Combined With Regorafenib as A Third-line Treatment in Patients With MSS CRLM

A Single-arm, Multicenter, Phase II Study to Evaluate the Efficacy and Safety of Candonilimab(AK104) Combined With Regorafenib For the Third-line Treatment of MSS Colorectal Liver Metastasis


Sponsor

Jin-hong Chen

Enrollment

44 participants

Start Date

Jul 11, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a single-arm, open-label, multicenter clinical study to evaluate the efficacy and safety of Candonilimab (AK104) combined with Regorafenib for the treatment of MSS colorectal liver metastasis. Candonilimab (AK104) is a humanized IgG1 bispecific antibody that targets PD-1 and CTLA-4.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Candonilimab (AK104) and a drug called Regorafenib for people with crc. The study is currently recruiting participants at 3 locations. 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGCandonilimab (AK104)

Cadonilimab (AK104): 6mg/kg, i.v. q2w.

DRUGRegorafenib

Regorafenib: 80 mg p.o. qd for 3 weeks of every 4 week cycle (i.e. 3 weeks on, 1 week off).


Locations(3)

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China

Huashan Hospital

Shanghai, China

Shanghai Tenth People's Hospital

Shanghai, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06455254


Related Trials