← Back to Clinical Trials
Recruiting Phase 2 NCT06758700

Post-line Treatment With Teniposide for c-Myc-driven Extensive-stage Small Cell Lung Cancer

Trial Parameters

Condition Extensive-stage Small Cell Lung Cancer (ES-SCLC)
Sponsor Shanghai Pulmonary Hospital, Shanghai, China
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 15
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2025-02-07
Completion 2026-06-30
Interventions
Teniposide administration

Brief Summary

The study is being conducted to investigate the efficacy and safety of teniposide in patients with extensive-stage small cell lung cancer who have failed standard treatment and with high expression of the c-Myc-driven FBXW2/MYC gene. Based on the results, the study will explore the correlation between the expression of FBXW2/MYC and the efficacy of teniposide.

Eligibility Criteria

Inclusion Criteria: 1. extensive stage small cell lung cancer 2. Progression after receiving at least one chemotherapy drug treatment in the past; 3. ECOG score 0-1 4. c-Myc-driven 5. Expected survival period ≥3 months 6. Age: 18-75 years old; 7. The informed consent form complies with the ICH-GCP principles. Exclusion Criteria: 1. No measurable lesions 2. Other severe and persistent diseases or organ system dysfunction; 3. Women planning pregnancy or men planning family planning; 4. Women who are pregnant or breastfeeding; 5. Those who cannot follow the research protocol provided by the investigator.

Related Trials