Image

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

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

Recruiting
18-75 years
All
Phase 2

Powered by AI

Overview

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

Description

This study will evaluate the efficacy of A166 in patients with HER2-positive unresectable or metastatic breast cancer previously treated with TOP1 inhibitor Antibody-Drug Conjugates.

A166 will be administered every 3 weeks (Q3W) intravenous (IV) infusion.

Eligibility

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.

Study details
    Her 2 Positive Breast Cancer

NCT07299825

Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.

1 February 2026

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.