Phase 2 Lung Cancer Trial, Recruiting NCT06739928 Sponsor: Guangzhou Institute of Respiratory Disease Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06739928
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 have been diagnosed with small cell lung cancer (SCLC) that has spread widely through the body (called "extensive-stage"), confirmed by a tissue or cell sample
  • People who have not yet received any treatment directed at the whole body (such as chemotherapy) for this cancer
  • People whose previous cancer treatment (radiation or chemotherapy) was completed at least 6 months before being diagnosed with extensive-stage SCLC
  • People who have at least one measurable area of cancer in the body that has not been previously treated with radiation
  • People aged 18 to 70 years old
  • People who are generally well enough to carry out everyday activities with no or minimal limitations (confirm with trial site for exact fitness score)
  • People who are expected to live for at least 12 weeks
  • People whose blood counts, liver, kidney, and clotting function all fall within acceptable ranges as determined by blood tests (confirm with trial site for specific values)
  • People who agree to use reliable contraception from the first dose of the study treatment until 6 months after the last dose; women who could become pregnant must have a negative pregnancy test within 7 days before enrolling
  • People who have been fully informed about the study and have signed a consent form agreeing to take part

Who may not be able to join:

  • People whose lung cancer is confirmed to be a mix of small cell and non-small cell lung cancer types
  • People who have previously been treated with immune checkpoint inhibitor drugs, or with irinotecan or similar drugs that work by blocking a specific enzyme (DNA topoisomerase inhibitors)
  • People who have taken certain medications that strongly affect how the body processes drugs (strong CYP3A4 inducers within 2 weeks, or strong CYP3A4 or UGT1A1 inhibitors within 1 week before starting the trial drug — confirm with trial site for specific medication examples)
  • People who have brain metastases, cancer spread to the lining of the brain or spinal cord, or spinal cord compression that is causing symptoms
  • People who have a blood or bone marrow disorder such as lymphoma, leukaemia, multiple myeloma, aplastic anaemia, or myelodysplastic syndrome
  • People who have significant fluid build-up around the heart, lungs, or abdomen that cannot be managed with drainage or other treatments
  • People who have an active, known, or suspected disease in which the immune system attacks the body (autoimmune disease)
  • People who have used corticosteroids above a low threshold dose, or other medicines that suppress the immune system, within 14 days before starting the trial drug
  • People who have received a live vaccine, or plan to receive one, within 4 weeks before starting the trial drug
  • People who have a lung condition involving scarring or inflammation of lung tissue, or active pneumonia causing symptoms, or severely reduced lung function
  • People who have active tuberculosis, or had active tuberculosis within the past 48 weeks
  • People who still have significant side effects from previous cancer treatments that have not settled down sufficiently before starting the trial drug
  • People who had a minor surgical procedure (including insertion of a catheter) within 48 hours before starting the trial drug
  • People who have uncontrolled heart or blood vessel problems
  • People who are known to be allergic to the trial drug or any of its ingredients
  • People who have had another cancer within the past 5 years, except for certain treated skin cancers or very early-stage cancers that were fully treated (confirm with trial site)
  • People with a history of psychiatric disorders, alcohol misuse, drug misuse, or substance misuse
  • People with certain active or chronic viral infections including hepatitis B (with elevated virus levels), hepatitis C, or HIV/AIDS
  • People who have taken part in another clinical trial or received another experimental drug within 4 weeks before signing the consent form
  • People who have previously had a bone marrow transplant or organ transplant from another person
  • People who are considered ineligible for any other reason as determined by the treating doctor at the trial site

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 8 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: Chengzhi Zhou, Doctor, Guangzhou Institute of Respiratory Disease (Responsible Party)

Phone: 13560351186

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
Guangzhou Institute of Respiratory Disease
Registry
ClinicalTrials.gov
Start date
1 January 2025
Est. completion
30 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

1-year OS rate

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: 8 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