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Not Yet RecruitingNCT06578286

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

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

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGARX788ARX788,1.5 mg/kg IV infusion on Day 1 of each 21-day treatment cycle

Timeline

Start date
2024-09-30
Primary completion
2026-09-30
Completion
2030-09-30
First posted
2024-08-29
Last updated
2024-08-29

Source: ClinicalTrials.gov record NCT06578286. Inclusion in this directory is not an endorsement.

ARX788 in HER2-positive Metastatic Breast Cancer Patients Who Were Previously Treated With T-DXd (NCT06578286) · Clinical Trials Directory