RecruitingPhase 2NCT05926700

Efficacy and Safety of Cadonilimab Plus Anlotinib in Advanced STS That Failed the Previous First-line Standard Treatment

Efficacy and Safety of Cadonilimab Combined With Anlotinibin in the Treatment of Advanced or Metastatic Soft Tissue Sarcoma With Previous First-Line Standard Treatment Failure.


Sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Enrollment

27 participants

Start Date

Feb 28, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Objective to evaluate the efficacy and safety of candonilimab combined with anlotinib in the treatment of progressive or metastatic soft tissue sarcoma that failed previous first-line standard therapy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of two drugs — cadonilimab (an immunotherapy) and anlotinib (a targeted therapy) — for people with advanced soft tissue sarcoma (a cancer of the muscles, fat, or connective tissue) that has stopped responding to standard chemotherapy. **You may be eligible if...** - You are between 18 and 70 years old - You have advanced or inoperable soft tissue sarcoma confirmed by biopsy - You have already tried at least one chemotherapy regimen (including an anthracycline drug) and your cancer has progressed - You have at least one tumor that can be measured on a scan - Your general health (ECOG score) is 0 or 1 - Your blood counts and organ function meet the required levels **You may NOT be eligible if...** - You have previously received immunotherapy (such as anti-PD-1 or anti-PD-L1 drugs) - You have an active autoimmune disease requiring treatment - You are currently taking immune-suppressing drugs - You have active hepatitis B or C, or HIV - You had a stroke, heart attack, or serious clotting event in the last 6 months - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

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

DRUGCandonilimab

The patients were treated with Candonilimab + anlotinib, with Cadonilimab 10mg/kg, D1 administration; Anlotinib 12mg/ day was orally administered for 2 weeks and stopped for a week, with 21 days as a course of treatment.


Locations(1)

The Second Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, China

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NCT05926700


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