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

Starting soon · Phase 3

Conditions studied: Triple Negative Breast Cancer

In brief

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.

Key facts

Study ID

NCT07679360

Run by

Suzhou Suncadia Biopharmaceuticals Co., Ltd.

People needed

1000

Starts

2026-07-01

Expected to finish

2032-12-01

Last updated by the study team

2026-07-01

Who can join

Age: 18 and older, up to 75. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Pathologically confirmed invasive triple negative breast cancer.
• Pathologic evidence of residual invasive carcinoma in the breast or axillary lymph nodes following completion of preoperative therapy.
• Previous neoadjuvant therapy must meet the requirements of the protocol.
• Has received radical surgery for breast cancer.
• ECOG PS 0\~1.
• Adequate organ functions.
• Women of childbearing potential must be willing to use highly effective form of contraception.

You may not qualify if…

• Stage IV metastatic breast cancer.
• Previous invasive breast cancer or ductal carcinoma in situ.
• Bilateral breast cancer.
• Any clinical evidence indicating the exist of recurrent diseases after surgery.
• History of other malignancy within the last 5 years, excluding cured skin basal cell carcinoma and cervical carcinoma in situ.
• Previously received antibody coupled drug (ADC) therapy with topoisomerase inhibitors as effective payloads.
• Previously received HER2 targeted therapy.
• Active or previously recorded autoimmune or inflammatory diseases.
• History of immunodeficiency.
• Participants with known or suspected interstitial pneumonia.
• Presence of active Hepatitis B.
• Known to have active tuberculosis infection.
• Uncontrolled infections requiring intravenous injection of antibiotics, antiviral drugs, or antifungal drugs for treatment.
• Within the 6 months prior to randomization, there was a history of myocardial infarction, severe/unstable angina, symptomatic congestive heart failure, ≥ Grade 2 supraventricular or ventricular arrhythmias, and any grade of ventricular fibrillation.
• Known allergy to any investigational drug or its excipients.
• Other medical conditions that would interfere with study participation or follow-up.

Where it is running

• Cancer Hospital of Chinese Academy of Medical Sciences — Beijing, Beijing Municipality, China

Full record on ClinicalTrials.gov

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