Phase 2 Lung Cancer Trial, Recruiting NCT06388031 Sponsor: Peking Union Medical College Hospital Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06388031
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 fully understand the study and are willing to sign a consent form agreeing to participate
  • People aged between 18 and 80 years old, of any gender
  • People who have been diagnosed with stage III or IV non-small cell lung cancer (a type of lung cancer), confirmed through a tissue or cell sample test
  • People who have previously been treated with a first-line immunotherapy drug (a type of cancer treatment that helps the immune system fight cancer) — either alone or combined with chemotherapy — for at least 35 treatment cycles, or whose cancer was stable for at least 2 years, and whose cancer has since gotten worse
  • People who have at least one measurable tumour that can be tracked on scans, according to standard measurement guidelines
  • People whose general health and ability to carry out daily activities falls within an acceptable range on a standard medical scale (confirm with trial site)
  • People whose blood, kidney, liver, and clotting function results meet the required levels on laboratory tests (confirm with trial site for specific values)
  • People who are willing and able to attend all required study visits, follow the treatment plan, and complete all study procedures
  • Women who could become pregnant, and men whose partners could become pregnant, who agree to use highly effective contraception throughout the study and for 180 days after the last dose of the study drug

Who may not be able to join:

  • People who have already had two or more previous systemic (whole-body) cancer treatments
  • People known to have certain specific genetic changes in their cancer cells (a sensitive EGFR mutation or ALK rearrangement) that can be targeted by other specific treatments
  • People who have cancer that has spread to the brain or the lining around the brain and is causing symptoms or getting worse
  • People with a history of, or currently active, autoimmune disease (where the immune system attacks the body), immune system deficiency, or who need ongoing steroid or immune-suppressing medication — though a history of an underactive thyroid, or well-controlled stable type 1 diabetes, may be exceptions (confirm with trial site)
  • People with certain types of lung scarring or inflammation conditions, including those who have needed steroid treatment for a lung inflammation condition in the past
  • People with known active tuberculosis, HIV infection, active hepatitis B or C, or other active infections currently requiring treatment
  • People who have received certain immune-stimulating treatments within 4 weeks before starting the study, or within 5 half-lives of that drug, whichever is the longer period
  • People who are pregnant, breastfeeding, planning to become pregnant, or planning to father a child from the screening visit through to 180 days after the last dose of the study drug
  • People who have previously had an organ or tissue transplant from another person, or who have other conditions that make immunotherapy unsuitable for them

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 19 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: Minjiang Chen, MD., Peking Union Medical College Hospital

Phone: +8618618340880

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
Registry
ClinicalTrials.gov
Start date
9 August 2024
Est. completion
10 January 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression Free Survival (PFS)

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: 19 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