Phase 2 Lung Cancer Trial, Recruiting NCT06607770 Sponsor: Zhou Chengzhi Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06607770
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 multiple separate lung cancers (confirmed by both clinical assessment and tissue testing)
  • People who had 3 or more lung nodules at the time of their first diagnosis or before surgery, with no spread to the lymph nodes
  • People whose largest lung nodule measures 3 cm (about 1.2 inches) or less across
  • People who have already had surgery to remove at least one nodule, with 2 or more nodules still remaining, and where post-surgery testing confirmed those remaining nodules are a very early, minimally invasive type of cancer (MIA or AIS)
  • People who are expected to have at least 1 measurable nodule remaining after a freezing treatment (cryotherapy), based on standard measurement guidelines
  • People aged 18 to 75 years old, of any gender
  • People who are generally well enough to carry out daily activities with little or no limitation, based on a standard health scoring system (ECOG score of 0 or 1)
  • People whose life expectancy is estimated to be at least 12 weeks
  • People whose blood counts, liver, and kidney function meet specific healthy ranges as tested by blood tests (confirm with trial site for exact values)
  • People who are willing and able to use an approved form of contraception during treatment and for 6 months after treatment ends (if applicable)
  • People who are able to give written consent and follow the trial's visit schedule and procedures

Who may not be able to join:

  • People whose cancer has specific genetic changes known as EGFR mutations or ALK rearrangements
  • People whose cancer cannot safely be treated with cryotherapy — for example, nodules spread widely through both lungs, extensive spread to the lining of the lungs with large fluid build-up, or tumours growing around major blood vessels in the chest
  • People who have previously been treated with certain immune-based therapies, including anti-PD-1, anti-PD-L1, or anti-CTLA-4 drugs, or similar treatments that affect immune system checkpoints
  • People who received chemotherapy, targeted therapy, immunotherapy, or any experimental drug within 4 weeks before joining the trial
  • People who received high-dose steroid medications (above a certain daily threshold) within the 4 weeks before joining
  • People who had major surgery within the 4 weeks before joining, or who have wounds, ulcers, or fractures that have not yet healed
  • People with a known or suspected active autoimmune condition (a condition where the immune system attacks the body's own tissues)
  • People who have had an organ transplant (other than a corneal transplant) or a bone marrow/stem cell transplant from a donor
  • People who have a known allergy to any ingredient in the study drug
  • People with interstitial lung disease (a condition causing scarring or inflammation in the lungs)
  • People with other serious medical conditions that are not well controlled
  • People with other significant illness, mental health conditions, or abnormal test results that the trial doctors believe could affect safety or the accuracy of trial results

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 13 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, The First Affiliated Hospital of Guangzhou Medical University,Guangzhou

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
Zhou Chengzhi
Registry
ClinicalTrials.gov
Start date
1 September 2024
Est. completion
1 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

irAEs 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: 13 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