RecruitingPhase 2NCT06165380

Cardenilimab Combined With Chemotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma

A Prospective, Multicenter, Phase II Study on the Efficacy and Safety of Cardenilimab Combined With Chemotherapy in the Conversion Therapy of Locally Advanced Esophageal Squamous Cell Carcinoma.


Sponsor

Li Zhang

Enrollment

43 participants

Start Date

Oct 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this trial is to test the efficacy and safety of cardenilimab combined with chemotherapy in the conversion therapy of locally advanced unresectable esophageal squamous cell carcinoma. type of study: clinical trial


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests cardenilimab — a dual checkpoint inhibitor that targets both PD-1 and LAG-3 — combined with chemotherapy for locally advanced cervical cancer. The goal is to see if adding this immunotherapy to standard chemoradiation improves outcomes. **You may be eligible if...** - You are 18 or older with locally advanced cervical cancer (confirmed by biopsy) - Your cancer has not spread to distant organs - You have not received prior treatment for this cancer - Your general health and organ function are adequate (ECOG 0–1) **You may NOT be eligible if...** - Your cancer has spread to distant organs (metastatic) - You have autoimmune disease requiring systemic treatment - You have had prior pelvic radiation - You are pregnant or breastfeeding - You have active hepatitis or HIV 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

DRUGCardenilimab Combined With Chemotherapy

Cardenilimab Combined With Chemotherapy


Locations(1)

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

Wuhan, Hubei, China

View Full Details on ClinicalTrials.gov

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NCT06165380


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