Clinical trial · Interventional
A Phase Ib/II Study of SHR-A1811 Injection in Breast Cancer
A Phase Ib/II Multicenter, Open-Label Clinical Trial of SHR-A1811 Injection in Combination With Pyrotinib or Pertuzumab or Adebrelimab or Paclitaxel for Injection (Albumin Bound) in Breast Cancer
NCT05353361CI-TRIAL-00069647unknownPhase 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)
To evaluate the safety, tolerability and efficacy of SHR-A1811 in combination with pyrotinib or pertuzumab or adebrelimab or albumin-bound paclitaxel in patients with 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 |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SHR-A1811;Adebrelimab | Drug | — | UNRESOLVED |
| SHR-A1811;Albumin paclitaxel | Drug | — | UNRESOLVED |
| SHR-A1811;Pertuzumab | Drug | — | UNRESOLVED |
| SHR-A1811:Pyrotinib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- SHR-A1811combined Pyrotinib
- interventionNames
- Drug: SHR-A1811:Pyrotinib
- type
- EXPERIMENTAL
- label
- SHR-A1811Combined Pertuzumab
- interventionNames
- Drug: SHR-A1811;Pertuzumab
- type
- EXPERIMENTAL
- label
- SHR-A1811Combined Adebrelimab
- interventionNames
- Drug: SHR-A1811;Adebrelimab
- type
- EXPERIMENTAL
- label
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. 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. Presence with uncontrollable third space effusion 4. Have undergone other anti-tumor treatment within 4 weeks before the first dose 5. Immunosuppressant or systemic hormone therapy was used within 2 weeks prior to the first dose 6. Any active autoimmune disease or a history of autoimmune disease 7. A history of immune deficiency 8. Clinically significant cardiovascular disorders 9. Clinically significant history of lung disease 10. The toxicity from previous anti-tumor treatment has not recovered to ≤ grade I 11. Known hereditary or acquired bleeding tendency 12. Active hepatitis and liver cirrhosis 13. Presence of other serious physical or mental diseases or laboratory abnormalities
References
Publications (0)
Data not yet available
No reference posted for this study.