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NCT Number: NCT06578286

ARX788 in HER2-positive Metastatic Breast Cancer Patients Who Were Previously Treated With T-DXd

A single arm, phase 2 Study of ARX788 in HER2-positive metastatic breast cancer patients who were previously treated with T-DXd. The ARX788 will be administered every 3 weeks (Q3W) intravenous (IV) infusion.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 to 75 years old (including upper and lower limits), male or female;
  • Unresectable locally advanced, recurrent or metastatic BC;
  • Tissue samples determined to be HER2 positive (defined as IHC3+ or FISH+);
  • Received T-DXd treatment in the advanced stage;
  • Adequate bone marrow, liver, kidney and coagulation function;
  • Voluntarily sign the informed consent, have good compliance and are willing to comply with the follow-up visit.

Exclusion criteria

  • With meningeal metastases or disseminated brain metastases or active brain metastases;
  • Has interstitial lung disease requiring steroid therapy, a history of drug-induced interstitial lung disease, a history of radiation pneumonitis, or any evidence indicating clinically active interstitial lung disease;
  • Has any eye disease that require medical intervention such as keratitis, corneal diseases or active eye infection;
  • Has cardiac insufficiency;
  • Has received any systemic anti-tumor therapy (with the exception of endocrine therapy, with an interval of at least 7 days) within 28 days (or at least 5 half-lives) before the first use of the investigational product;

Treatment and study plan

ARX788

Drug

ARX788,1.5 mg/kg IV infusion on Day 1 of each 21-day treatment cycle

Primary outcomes

  1. Objective remission rate (ORR)

    Time frame: Until progression, assessed up to approximately 24 months

    The proportion of patients who have a CR or PR, as determined by the Investigator at local site per RECIST 1.1.

Secondary outcomes

  1. Disease control rate (DCR)

    Time frame: Baseline through end of study, assessed up to 24 months]

    The proportion of patients who have a CR or PR or SD, as determined by the Investigator at local site per RECIST 1.1.

  2. Duration of relief (DOR)

    Time frame: Until progression, assessed up to approximately 24 months

    Time from the date of first documented response until the date of documented progression or death in the absence of disease progression

  3. Progression-free survival (PFS)

    Time frame: Until progression or death, assessed up to approximately 36 months]

    Time to progression as assessed by the Investigator at local site per RECIST 1.1, or death due to any cause.

  4. Overall survival (OS)

    Time frame: Until death, assessed up to approximately 50 months

    Time to death due to any cause

  5. The number of subjects experiencing adverse event TEAEs

    Time frame: Up to follow-up period, approximately 50 months

    Occurrence of AEs according to CTCAE v5.0

Study contacts

Contact information is provided by the study sponsor or research team.

Jian Zhang, MD,PhD

CONTACT

[email protected]

+8664175590 ext. 85000

Yanchun Meng, MD

CONTACT

[email protected]

+8664175590 ext. 85000

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Official study title

Evaluate the Efficacy and Safety of ARX788 in Patients With HER2-positive Advanced Breast Cancer Whose Disease Has Progressed Following T-DXd Therapy

Important dates

Study start
2024
Primary completion
2026
Study completion
2030
First posted
Aug 29, 2024
Registry last updated
Aug 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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