RecruitingPhase 3NCT07679360

A Study of Trastuzumab Rezetecan in Combination With Adebrelimab Versus Investigator's Choice of Therapy in Subjects With Residual Triple Negative Breast Cancer

A Phase III, Multicenter, Randomized, Open-Label Parallel-Controlled Study of Trastuzumab Rezetecan (SHR-A1811) in Combination With Adebrelimab (SHR-1316) Versus Investigator's Choice of Therapy in Subjects With Primary Triple Negative Breast Cancer Who Have Residual Invasive Disease Following Neoadjuvant Therapy


Sponsor

Suzhou Suncadia Biopharmaceuticals Co., Ltd.

Enrollment

1,000 participants

Start Date

Sep 2, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

It is a randomized, open label, positive drug controlled, multicenter design Phase III clinical trial, aims to compare the efficacy and safety of SHR-A1811 combined with Adebrelimab and the treatment selected by the researchers in the adjuvant treatment of triple negative breast cancer with invasive residual cancer after neoadjuvant treatment, and to explore the PK characteristics and immunogenicity of SHR-A1811 and Adebrelimab.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Adebrelimab Injection, a drug called Capecitabine tablets, and others for people with triple-negative breast cancer. The study is currently recruiting participants at 1 location. People eligible for this study include women 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

DRUGTrastuzumab Rezetecan for Injection

Trastuzumab Rezetecan for Injection.

DRUGAdebrelimab Injection

Adebrelimab Injection.

DRUGCapecitabine tablets

Capecitabine Tables.

DRUGPembrolizumab injection

Pembrolizumab Injection.


Locations(1)

Cancer Hospital of Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

View Full Details on ClinicalTrials.gov

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NCT07679360


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