Clinical trial · Interventional
A Phase III Study of SHR-A1811 Injection With or Without Pertuzumab in HER2-Positive Recurrent or Metastatic Breast Cancer
A Phase III Multicenter, Randomized, Open-label, Active-Controlled Study of SHR-A1811 With or Without Pertuzumab Versus Trastuzumab, Pertuzumab and Docetaxel in HER2-Positive Recurrent or Metastatic Breast Cancer
NCT06057610CI-TRIAL-00105261active not recruitingPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 10, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260910-000001
Summary
Brief summary (as posted)
To evaluate the efficacy and safety of SHR-A1811 with or without pertuzumab versus trastuzumab, pertuzumab and docetaxel in HER2-Positive Recurrent or Metastatic Breast Cancer
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 |
|---|---|---|---|
| HER2-PositiveRecurrent or Metastatic Breast Cancer | Breast Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SHR-A1811 Injection | Drug | — | UNRESOLVED |
| SHR-A1811 Injection ; Pertuzumab Injection | Drug | — | UNRESOLVED |
| Trastuzumab Injection;Pertuzumab Injection ; Docetaxel Injection | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Treatment group A: SHR-A1811 Injection
- interventionNames
- Drug: SHR-A1811 Injection
- type
- EXPERIMENTAL
- label
- Treatment group B: SHR-A1811 Injection and Pertuzumab Injection
- interventionNames
- Drug: SHR-A1811 Injection ; Pertuzumab Injection
- type
- ACTIVE_COMPARATOR
- label
- Treatment group C: Trastuzumab Injection, Pertuzumab Injection and Docetaxel Injection
- interventionNames
- Drug: Trastuzumab Injection;Pertuzumab Injection ; Docetaxel Injection
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Women aged 18 to 75 (inclusive) 2. HER2 positive (IHC3+ or ISH+) unresectable or metastatic breast cancer confirmed by histology or cytology. 3. ECOG score is 0 or 1 4. An expected survival of ≥ 12 weeks 5. At least one measurable lesion according to RECIST v1.1 criteria 6. Have adequate renal and hepatic function 7. Patients voluntarily joined the study and signed informed consent Exclusion Criteria: 1. Have other malignancies within the past 5 years 2. Active central nervous system metastasis without surgery or radiotherapy 3. In (neoadjuvant) adjuvant therapy phase, the interval from the end of systemic therapy (excluding endocrine therapy) to the detection of recurrence/metastasis ≤12 months 4. Presence with uncontrollable third space effusion 5. Have undergone other anti-tumor treatment within 4 weeks before the first dose 6. A history of immune deficiency 7. Clinically significant cardiovascular disorders 8. Known or suspected interstitial lung disease 9. The toxicity from previous anti-tumor treatment has not recovered to ≤ grade I 10. Known hereditary or acquired bleeding tendency 11. Active hepatitis and liver cirrhosis 12. Presence of other serious physical or mental diseases or laboratory abnormalities
References
Publications (0)
Data not yet available
No reference posted for this study.