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OncoMatch/Clinical Trials/NCT06475300

A Study of BL-B01D1+PD-1 Monoclonal Antibody in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer, Nasopharyngeal Carcinoma and Other Solid Tumors

Is NCT06475300 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including BL-B01D1 and PD-1 Monoclonal Antibody for non-small cell lung cancer.

Phase 2RecruitingSichuan Baili Pharmaceutical Co., Ltd.NCT06475300Data as of May 2026

Treatment: BL-B01D1 · PD-1 Monoclonal AntibodyThis phase II study is a clinical study to explore the efficacy and safety of BL-B01D1 combined with PD-1 Monoclonal Antibody in patients with locally advanced or metastatic non-small cell lung cancer, nasopharyngeal carcinoma and other solid tumors.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Head and Neck Squamous Cell Carcinoma

Tumor Agnostic

Biomarker criteria

Excluded: ALK fusion

Excluded: EGFR sensitizing mutation

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: systemic chemotherapy

Stage 1 EGFR-sensitive mutant non-small cell lung cancer patients with systemic chemotherapy

Cannot have received: systemic therapy

Stage 2 patients who had received previous systemic therapy

Cannot have received: anti-tumor therapy (chemotherapy, biological therapy, mitomycin, nitrosoureas, fluorouracil class oral drugs)

Anti-tumor therapy such as chemotherapy or biological therapy has been used within 4 weeks or 5 half-lives before the first dose; Mitomycin and nitrosoureas were administered within 6 weeks before the first dose; Fluorouracil class oral drugs, etc.

Lab requirements

Cardiac function

no serious cardiac dysfunction, left ventricular ejection fraction 50% or higher

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

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