Phase 2 Lung Cancer Trial, Recruiting NCT06769971 Sponsor: Sichuan University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06769971
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are able to understand and willingly sign a consent form before any study procedures begin
  • People aged 18 to 75 years old at the time of signing the consent form
  • People with a good general health and activity level, rated 0 or 1 on a standard cancer performance scale (meaning fully active or able to carry out light work)
  • People with a life expectancy of at least 3 months
  • People who have been formally diagnosed with extensive stage small cell lung cancer (a type of lung cancer that has spread), confirmed through a tissue or cell sample
  • People who have not previously received systemic (whole-body) treatment for this cancer, OR people with extensive stage small cell lung cancer who previously received chemotherapy and radiation for an earlier, more limited stage of the disease, but whose cancer came back more than 6 months after that treatment ended
  • People who have at least one measurable area of cancer that can be tracked using standard imaging assessment criteria
  • People who are able to provide a stored tumour tissue sample (a specific type of preserved biopsy sample)
  • People whose kidneys, liver, blood, and other organs are functioning adequately (confirm with trial site for specific thresholds)
  • People of reproductive potential who agree to use an effective method of contraception during the study and for 120 days after the last dose of the study treatment

Who may not be able to join:

  • People who have had another active cancer in the past 5 years, other than the cancer being studied in this trial or a previously cured localised cancer
  • People who received certain local treatments or immune-modulating treatments within 2 weeks before the first dose, or certain Chinese herbal or traditional medicines with anti-cancer indications within 1 week before the first dose
  • People who have previously received any treatment that targets the body's immune system to fight tumours
  • People who have previously received any treatment designed to block the growth of blood vessels that feed tumours
  • People whose tumour surrounds major blood vessels, shows significant breakdown or cavitation, or has grown into nearby important organs or blood vessels
  • People who have had an active autoimmune disease requiring systemic treatment at any point in the 2 years before starting the study
  • People who have cancer that has spread to the brain or spinal cord and is causing symptoms
  • People with significant fluid build-up around the lungs, heart, or abdomen that requires frequent draining
  • People who have had a hole or abnormal opening in the digestive tract, a bowel blockage requiring special nutrition, or major bowel surgery within 6 months before the first dose
  • People with a known active Hepatitis B or Hepatitis C infection
  • People who have had a heart attack, unstable chest pain, or heart or blood vessel surgery or procedures within 12 months before the study starts
  • People who have had a serious infection within 4 weeks before the first dose, or who have been on systemic anti-infective treatment within 2 weeks before the first dose (not including hepatitis B or C antiviral therapy)
  • People currently enrolled in another clinical trial that involves an active treatment, unless the last dose of that trial's treatment was more than 4 weeks ago or more than 5 half-lives of that drug ago (whichever is shorter)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Yongsheng Wang, Prof, West China Hospital

Phone: 86(028)85421606

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Sichuan University
Registry
ClinicalTrials.gov
Start date
1 February 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

ORR; Safety

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov