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OncoMatch/Clinical Trials/NCT06786026

QL1706 Plus Chemotherapy +/- Bevacizumab in 1L Treatment of R/mTNBC

Is NCT06786026 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including bevacizumab and QL1706 for tnbc, triple negative breast cancer.

Phase 2RecruitingFudan UniversityNCT06786026Data as of Jun 2026Location: China

Treatment: bevacizumab · QL1706 · Nab paclitaxelThis study is to evaluate the efficacy and safety of QL1706 plus albumin-bound paclitaxel ± bevacizumab in 1L treatment of r/mTNBC

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Extracted eligibility criteria

Treatments studied

Targeted therapy

bevacizumab

Chemotherapy

Nab paclitaxel

Other

QL1706

Cancer type

Triple-Negative Breast Cancer

Breast Carcinoma

Biomarker criteria

Required: HER2 (ERBB2) negative (negative)

Required: ESR1 negative (negative)

Required: PR (PGR) negative (negative)

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75
Female only

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Lab requirements

Blood counts

Absolute neutrophil count ≥1.5×10^9/L; Platelets ≥100×10^9/L; Hemoglobin ≥90 g/L

Kidney function

Serum creatinine ≤1.5×ULN

Liver function

Serum total bilirubin ≤1.5×ULN, if liver metastasis is present, ≤3ULN; ALT and AST ≤2.5×ULN, if liver metastasis is present, ALT and AST ≤5ULN; AKP≤2.5×ULN

Adequate organ function (no blood components or cell growth factor drugs are allowed within 14 days before the first medication): (1) Absolute neutrophil count ≥1.5×10^9/L; (2) Platelets ≥100×10^9/L; (3) Hemoglobin ≥90 g/L; (4) Serum albumin ≥30 g/L; (5) Thyroid-stimulating hormone (TSH) ≤1×ULN (if abnormal, the FT3 and FT4 levels should be examined at the same time. If the FT3 and FT4 levels are normal, you can be included in the group); (6) Serum total bilirubin ≤1.5×ULN,if liver metastasis is present, ≤3ULN; (7) ALT and AST ≤2.5×ULN, if liver metastasis is present, ALT and AST ≤5ULN; (8) AKP≤2.5×ULN; Serum creatinine ≤1.5×ULN; (9) International normalized ratio (INR) ≤1.5 (not receiving anticoagulant therapy).

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06786026 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require ERBB2?

Yes, ERBB2 negative is a required biomarker for enrollment.

Does this trial require ESR1?

Yes, ESR1 negative is a required biomarker for enrollment.

Does this trial require PGR?

Yes, PGR negative is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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