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Recruiting Phase 2

A Study of A166 in Patients With HER2-Positive Unresectable or Metastatic Breast Cancer

NCT07299825 · tracked via the Priya Life Science China tracker
Phase
Phase 2
Started
2024-09-20
Last updated
2026-05-08

Condition(s) studied

Her 2 Positive Breast Cancer

Investigational drug(s) / intervention(s)

A166 →

A166: intravenous(IV) infusion (Q3W)

Study summary

Evaluation of the efficacy of A166 in Patients with HER2-Positive unresectable or metastatic breast cancer previously treated with TOP1 inhibitor Antibody-Drug Conjugates

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Male or female patient ≥ 18 years and ≤ 75 years when signing the informed consent form. 2. Breast cancer patients by histopathology and/or cytology documented. 3. In the advanced or metastatic stage, having received no more than 5 lines of systemic therapy, one of which must include a HER2 ADC with a topoisomerase inhibitor payload. 4. Patients must have experienced disease progression or intolerance during or after the most recent treatment prior to randomization. 5. At least one measurable lesion according to RECIST 1.1 criteria. Exclusion Criteria: 1. Previous treatment with A166 or any HER2-targeted antibody-drug conjugate (ADC) with a microtubule inhibitor payload. 2. Known history of severe hypersensitivity to other monoclonal antibodies, or allergy to A166 or their components. 3. Permanent discontinuation of trastuzumab or its biosimilars due to any toxicity in prior treatments. 4. Presence of severe corneal epithelial disease at baseline; or inability to perform daily activities without contact lenses. 5. Presence of spinal cord compression or clinically active central nervous system (CNS) metastases. 6. Other conditions considered by the investigator to make the patient unsuitable for participation in the study.

Primary outcome measure(s)

  • Objective response rate(ORR) — Within 24 months of last patient enrolled
    ORR is defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by investigator per RECIST 1.1

Trial sites (1)

FacilityCityRegionStatus
Henan Provincial Cancer Hospital Zhenzhou Henan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07299825 on ClinicalTrials.gov ↗ ← All trials in China