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OncoMatch/Clinical Trials/NCT07232420

A Study of BL-M24D1 in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer and Other Solid Tumors

Is NCT07232420 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies BL-M24D1 for non small cell lung cancer.

Phase 1RecruitingSichuan Baili Pharmaceutical Co., Ltd.NCT07232420Data as of Jun 2026Location: China

Treatment: BL-M24D1This study is an open, multicenter, non-randomized phase I clinical trial to evaluate the safety, tolerability, pharmacokinetic characteristics, and preliminary efficacy of BL-M24D1 in patients with locally advanced or metastatic non-small cell lung cancer and other solid tumors.

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Extracted eligibility criteria

Treatments studied

Other

BL-M24D1

Cancer type

Non-Small Cell Lung Carcinoma

Tumor Agnostic

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: chemotherapy

Use of chemotherapy...within 4 weeks or 5 half-lives prior to the first dose

Cannot have received: biotherapy

Use of...biotherapy...within 4 weeks or 5 half-lives prior to the first dose

Cannot have received: immunotherapy

Use of...immunotherapy within 4 weeks or 5 half-lives prior to the first dose

Cannot have received: anthracycline

Exception: cumulative dose ≤360 mg/m² in previous (neo)adjuvant anthracycline therapy

Cumulative dose of anthracyclines >360 mg/m² in previous (neo)adjuvant anthracycline therapy

Lab requirements

Blood counts

Toxicities from prior antitumor therapy have recovered to ≤ Grade 1 as defined by NCI-CTCAE v5.0

Kidney function

Liver function

Cardiac function

No severe cardiac dysfunction, left ventricular ejection fraction ≥50%; QT interval prolongation, complete left bundle branch block, or third-degree atrioventricular block excluded

No severe cardiac dysfunction, left ventricular ejection fraction ≥50%; Organ function levels must meet the requirements; Coagulation function: international normalized ratio ≤1.5, and activated partial thromboplastin time ≤1.5 × ULN; Urine protein ≤2+ or ≤1000mg/24h

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

Frequently asked questions

Is NCT07232420 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, biotherapy, immunotherapy disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

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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