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OncoMatch/Clinical Trials/NCT07045311

JS207 Combination Therapy in Triple-negative Breast Cancer

Is NCT07045311 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including JS207 in combination with 9MW2821 and JS207 in combination with Albumin paclitaxel for triple-negative breast cancer.

Phase 2RecruitingShanghai Junshi Bioscience Co., Ltd.NCT07045311Data as of May 2026

Treatment: JS207 in combination with 9MW2821 · JS207 in combination with Albumin paclitaxelThis is an open-label, multi-center, phase II clinical study to preliminarily evaluate the efficacy and safety of JS207 combined with 9MW2821 or albumin paclitaxel as first-line therapy in patients with recurrent or metastatic TNBC.

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Extracted eligibility criteria

Cancer type

Triple-Negative Breast Cancer

Breast Carcinoma

Biomarker criteria

Required: HER2 (ERBB2) wild-type

Required: ESR1 wild-type

Required: PR (PGR) wild-type

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Cannot have received: anti-PD-1/PD-L1/PD-L2 or co-inhibitory T-cell receptor therapy

Exception: in (new) adjuvant therapy is allowed, if DFI is ≥6 months

Previous treatment with anti-PD-1, anti-PD-L1 or anti-PD-L2 drugs or drugs targeting other stimulatory or co-inhibitory T cell receptors (e.g., CTLA-4, OX-40, CD137) in (new) adjuvant therapy is allowed, if DFI is ≥6 months

Cannot have received: antibody-drug conjugate (Enfortumab Vedotin)

previously treated with Antibody-Drug Conjugates conjugated with MMAE and/or targeting Nectin-4, such as Enfortumab Vedotin is not allowed

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function

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

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