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

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

Recruiting
18-75 years
All
Phase 2

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Overview

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

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.

Study details
    Extensive-stage Small Cell Lung Cancer (ES-SCLC)
    Thoracic Neoplasms
    Lung Neoplasms
    Lung Diseases

NCT06758700

Shanghai Pulmonary Hospital, Shanghai, China

1 February 2026

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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