Clinical trial · Interventional
Efficacy and Safety of BGB-290 in the Treatment of Metastatic HER2-Negative Breast Cancer Patients With BRCA Mutation in China
An Open Label, Multi-Center Phase 2 Study to Evaluate Efficacy and Safety of BGB-290 in the Treatment of Metastatic HER2-Negative Breast Cancer Patients With BRCA Mutation in China
NCT03575065CI-TRIAL-00081960completedPhase 2Results postedClinicalTrials.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)
This is a Phase 2, open-label, multi-center study of BGB-290 administered orally (PO) twice daily (BID) in adult Chinese patients with advanced HER2(-) breast cancer harboring germline BRCA mutation, which have progressed despite standard therapy, or for which no standard therapy exists.
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-negative Breast Cancer | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| BGB-290 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Cohort 1: Triple-negative breast cancer (TNBC)
- description
- Locally advanced or metastatic TNBC
- interventionNames
- Drug: BGB-290
- type
- EXPERIMENTAL
- label
- Cohort 2: HR(+)/HER2(-) breast cancer
- description
- Locally advanced or metastatic Hormone receptor-positive(HR+) human epidermal growth factor receptor2 Negative(HER2-) breast cancer
- interventionNames
- Drug: BGB-290
Primary outcomes (1)
- measure
- Objective Response Rate (ORR) as Assessed by Independent Radiology Review (IRC)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Confirmed deleterious or suspected deleterious germline BRCA1 or BRCA2 mutation 2. Locally advanced or metastatic breast cancer despite standard therapy and the following: 1. Histologically or cytologically confirmed HER2(-) breast cancer (TNBC or estrogen receptor-positive and/or PR+) 2. ≤ 2 prior lines of chemotherapy in advanced or metastatic setting 3. Prior platinum therapy allowed as long as no disease progression while on treatment, or if given in neoadjuvant/adjuvant setting with ≥ 6 months from last platinum to relapse 4. Prior therapy with an anthracycline and/or a taxane in neoadjuvant/adjuvant or metastatic setting 5. Archival tumor tissues will be collected from all patients, if available 6. For HR(+)/HER2(-) breast cancer only: patients must have received and progressed on at least one endocrine therapy either in adjuvant or metastatic setting, or have disease that the treating physician believes to be inappropriate for endocrine therapy 3. Measurable disease as defined per RECIST, version 1.1 4. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1 5. Adequate hematologic and organ function Exclusion Criteria: 1. Unresolved acute effects of prior therapy of ≥ Grade 2 2. Prior treatment with a poly\[ADP-ribose\] polymerase (PARP) inhibitor 3. Chemotherapy, radiotherapy, biologic therapy, immunotherapy, investigational agent, anticancer Chinese medicine, or anticancer herbal remedies ≤ 14 days (or ≤ 5 half lives, if applicable, whichever is shorter) prior to Day 1 of Cycle 1 4. Major surgical procedure, open biopsy, or significant traumatic injury ≤ 14 days prior to Day 1 of Cycle 1, or anticipation of need for major surgical procedure during the course of the study 5. Diagnosis of myelodysplastic syndrome (MDS) 6. Other diagnosis of malignancy 7. Untreated and/or active brain metastases. 8. Active infection requiring systemic treatment, active viral hepatitis, or active tuberculosis 9. Clinically significant cardiovascular disease 10. Pregnancy or nursing 11. Known history of intolerance to the excipients of the BGB-290 capsule
References
Publications (2)
- BACKGROUNDXu B, Zhang QY, Yang H, Gu T, Zhang K, Liang J, Qiu JJ, Yang R, Zhang L, Mu S, Sun J, Huang V, Dong M. An Open-Label, Multicenter, Phase 2 Study to Evaluate the Antitumor Activity and Safety of Pamiparib in the Treatment of Metastatic HER2-Negative Breast Cancer Patients With BRCA Mutation in China. Chinese Society of Clinical Oncology. 2018.
- BACKGROUNDXu B, Sun T, Shi Y, Cui J, Yin Y, Ouyang Q, Liu Q, Zhang Q, Chen Y, Wang S, Wang X, Tong Z, Zhong Y, Wang J, Yan M, Yan X, Wang C, Feng J, Wang X, Hu G, Cheng Y, Ge R, Zhu Z, Zhang W, Shao Z. Pamiparib in patients with locally advanced or metastatic HER2-negative breast cancer with germline BRCA mutations: a phase II study. Breast Cancer Res Treat. 2023 Feb;197(3):489-501. doi: 10.1007/s10549-022-06785-z. Epub 2022 Dec 2. PMID 36459284