Clinical trial · Interventional
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
NCT06578286CI-TRIAL-00080320not yet recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ARX788 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ARX788
- description
- ARX788,1.5 mg/kg IV infusion on Day 1 of each 21-day treatment cycle
- interventionNames
- Drug: ARX788
Primary outcomes (1)
- measure
- Objective remission rate (ORR)
- timeFrame
- Until progression, assessed up to approximately 24 months
- description
- The proportion of patients who have a CR or PR, as determined by the Investigator at local site per RECIST 1.1.
Secondary outcomes (5)
- measure
- Disease control rate (DCR)
- timeFrame
- Baseline through end of study, assessed up to 24 months]
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. 18 to 75 years old (including upper and lower limits), male or female; 2. Unresectable locally advanced, recurrent or metastatic BC; 3. Tissue samples determined to be HER2 positive (defined as IHC3+ or FISH+); 4. Received T-DXd treatment in the advanced stage; 5. Adequate bone marrow, liver, kidney and coagulation function; 6. Voluntarily sign the informed consent, have good compliance and are willing to comply with the follow-up visit. Exclusion Criteria: 1. With meningeal metastases or disseminated brain metastases or active brain metastases; 2. 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; 3. Has any eye disease that require medical intervention such as keratitis, corneal diseases or active eye infection; 4. Has cardiac insufficiency; 5. 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;
References
Publications (0)
Data not yet available
No reference posted for this study.