A Study Comparing BL-B01D1 With Chemotherapy of Physician's Choice in Patients With Unresectable Locally Advanced or Metastatic Triple-Negative Breast Cancer

NCT ID: NCT06382142

Last Updated: 2025-11-17

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 418 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-06-21
• Study Completion Date: 2026-06-30

Brief Summary

This trial is a registered phase III, randomized, open-label, multicenter study designed to evaluate the efficacy and safety of BL-B01D1 in patients with unresectable locally advanced or metastatic Triple-Negative breast cancer after taxane failure.

Conditions

Triple-Negative Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

BL-B01D1

Participants receive BL-B01D1 as intravenous infusion for the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.

Group Type: EXPERIMENTAL

BL-B01D1

Intervention Type: DRUG

Administration by intravenous infusion for a cycle of 3 weeks.

Eribulin or Vinorelbine or Gemcitabine or Capecitabine

Participants receive Eribulin or Vinorelbine or Gemcitabine or Capecitabine in the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.

Group Type: EXPERIMENTAL

Eribulin

Intervention Type: DRUG

Administration by intravenous bolus for a cycle of 3 weeks.

Vinorelbine

Intervention Type: DRUG

Administration by intravenous infusion for a cycle of 3 weeks.

Gemcitabine

Intervention Type: DRUG

Administration by intravenous infusion for a cycle of 3 weeks.

Capecitabine

Intervention Type: DRUG

Oral administration for a cycle of 3 weeks.

Interventions

BL-B01D1

Administration by intravenous infusion for a cycle of 3 weeks.

Intervention Type: DRUG

Eribulin

Administration by intravenous bolus for a cycle of 3 weeks.

Intervention Type: DRUG

Vinorelbine

Administration by intravenous infusion for a cycle of 3 weeks.

Intervention Type: DRUG

Gemcitabine

Administration by intravenous infusion for a cycle of 3 weeks.

Intervention Type: DRUG

Capecitabine

Oral administration for a cycle of 3 weeks.

Intervention Type: DRUG

Other Intervention Names

iza-bren; izalontamab brengitecan; BMS-986507

Eligibility Criteria

Inclusion Criteria

1. Voluntarily sign the informed consent and follow the requirements of the protocol;

2. No gender limit;

3. Age ≥18 years old and ≤75 years old;

4. Expected survival time ≥3 months;

5. Patients with unresectable, locally advanced or metastatic triple-negative breast cancer;

6. Consent to provide archival tumor tissue samples or fresh tissue samples of primary or metastatic lesions within 3 years;

7. The subjects had received 1-2 lines of chemotherapy regimens in the locally advanced or metastatic stage, and had been treated with taxanes previously;

8. Acceptability of chemotherapy with eribulin, capecitabine, gemcitabine, or vinorelbine, as assessed by the investigator;

9. Patients with baseline brain metastases should have received treatment for all brain metastases and be stable;

10. Must have at least one measurable lesion that meets the RECIST v1.1 definition;

11. ECOG score 0 or 1;

12. Toxicity of previous antineoplastic therapy has returned to ≤ grade 1 defined by NCI-CTCAE v5.0;

13. No severe cardiac dysfunction, left ventricular ejection fraction ≥50%;

14. No blood transfusion, no use of cell growth factors and/or platelet raising drugs within 14 days before the first use of the study drug, and the organ function level must meet the requirements;

15. Coagulation function: international normalized ratio ≤1.5, and activated partial thromboplastin time ≤1.5×ULN;

16. Urine protein ≤2+ or < 1000mg/24h;

17. For premenopausal women with childbearing potential, a pregnancy test must be performed within 7 days before the initiation of treatment, serum pregnancy must be negative, and must be non-lactating; All enrolled patients (male or female) were advised to use adequate barrier contraception throughout the treatment cycle and for 6 months after the end of treatment.

Exclusion Criteria

1. Prior receipt of an ADC with a TOPI inhibitor as a toxin;

2. Prior receipt of an ADC or antibody drug targeting EGFR and/or HER3;

3. Chemotherapy, biological therapy, immunotherapy, etc. within 4 weeks or 5 half-lives before the first dose, small molecule targeted therapy within 5 days, palliative radiotherapy and anti-tumor therapy within 2 weeks;

4. Anthracycline equivalent cumulative dose of adriamycin > 360 mg/m2;

5. History of severe cardiovascular or cerebrovascular disease;

6. Unstable thrombotic events requiring therapeutic intervention within 6 months before screening;

7. QT prolongation, complete left bundle branch block, III degree atrioventricular block, frequent and uncontrollable arrhythmia;

8. Active malignancy diagnosed within 5 years before randomization;

9. Hypertension poorly controlled by two antihypertensive drugs;

10. Patients with poor blood glucose control before the first dose;

11. A history of interstitial lung disease requiring steroid therapy, or current radiation pneumonitis, or a suspicion of such disease;

12. Complicated with pulmonary diseases leading to clinically severe respiratory impairment;

13. Patients with carcinomatous meningitis (meningeal metastasis) or brain stem metastasis or spinal cord compression;

14. Have a history of allergy to recombinant humanized antibodies or any of the ingredients of BL-B01D1;

15. A history of autologous or allogeneic stem cell transplantation;

16. Human immunodeficiency virus antibody positive, active hepatitis B virus infection, or hepatitis C virus infection;

17. Severe infection within 4 weeks before randomization; Evidence of pulmonary infection or active pulmonary inflammation within 2 weeks before randomization;

18. Patients with massive or symptomatic effusions or poorly controlled effusions;

19. Imaging examination showed that the tumor had invaded or enveloped the large blood vessels in the abdomen, chest, neck, and pharynx;

20. Were receiving long-term systemic corticosteroids or equivalent active anti-inflammatory drugs or any form of immunosuppressive therapy before randomization;

21. Received other unmarketed investigational drug or treatment within 4 weeks before the first dose;

22. Patients with superior vena cava syndrome should not be rehydrated;

23. A history of severe neurological or mental illness;

24. Severe unhealed wound, ulcer, or fracture within 4 weeks before signing the informed consent;

25. Subjects with clinically significant bleeding or obvious bleeding tendency within 4 weeks before signing the informed consent;

26. History of intestinal obstruction, inflammatory bowel disease, or extensive bowel resection or presence of Crohn's disease, ulcerative colitis, or chronic diarrhea;

27. Patients scheduled for vaccination or receiving live vaccine within 28 days before the first dose;

28. Other circumstances that were assessed by the investigator as inappropriate for participation in the trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

Sichuan Baili Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jiong Wu

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Jian Zhang

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Locations

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

BL-B01D1-307

Identifier Type: -

Identifier Source: org_study_id