Phase 2 Lung Cancer Trial, Recruiting NCT06467617 Sponsor: Beijing Chest Hospital, Capital Medical University Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06467617
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 aged 18 to 75 years old, of any gender
  • People with a good general health and activity level (rated 0 or 1 on a standard medical scale, meaning fully active or able to carry out light work)
  • People who have been confirmed through tissue or cell testing to have non-small cell lung cancer (NSCLC) at stage II, IIIA, or a specific type of stage IIIB, where the cancer is expected to be fully removable by surgery, including nearby lymph nodes no larger than 2cm in short diameter
  • People who have at least one measurable tumour or affected lymph node of a minimum size, as measured on a CT scan using standard criteria
  • People who have not previously received any cancer treatment, including radiotherapy, chemotherapy, surgery, or targeted therapy
  • People whose lung function is strong enough to safely undergo surgery with the goal of completely removing the cancer
  • People whose blood test results meet specific minimum thresholds for white blood cells, haemoglobin, and platelets (without recent transfusions or blood-boosting medications)
  • People whose liver and kidney function test results fall within acceptable ranges as defined by the trial

Who may not be able to join:

  • People whose cancer has a known EGFR or ALK gene mutation
  • People whose tumour has grown into nearby critical structures such as the heart, major blood vessels, windpipe, voice nerve, food pipe, spine, or the upper part of the lung near the shoulder
  • People who have taken immune-suppressing medications in the 4 weeks before the first study treatment (with some exceptions for low-dose steroids and inhaled or nasal sprays)
  • People who have used herbal medicines or other substances known to affect the immune system in the 4 weeks before the first study treatment (with some exceptions)
  • People who have had a different type of cancer in the 5 years before joining the trial
  • People who have received a live vaccine within 4 weeks before the first study treatment, or who plan to receive one during the trial
  • People who are currently taking part in another clinical trial involving an investigational treatment, or who received such a treatment within 4 weeks before starting this trial, or who have not fully recovered from side effects of a previous medical procedure
  • People who have had a serious infection requiring intravenous antibiotics or antifungal/antiviral medications within 4 weeks before the first dose, or who have an unexplained fever above 38.5°C at the time of screening
  • People who have a history of, or suspected, pneumonia, interstitial lung disease, or any lung condition that would interfere with breathing tests
  • People with an active autoimmune disease or a history of autoimmune disease (people with childhood asthma that resolved completely without treatment, or with a skin condition called vitiligo, may still be considered)
  • People with immune system deficiencies such as HIV infection, active hepatitis B or C, or both hepatitis B and C together, or liver cirrhosis related to alcohol use
  • People with significant heart conditions, including moderate-to-severe heart muscle disease, poorly controlled irregular heartbeat, heart failure of grade III or IV, a heart ejection fraction below 50%, or a heart attack or serious heart event within the 6 months before joining
  • People whose liver enzyme levels (ALT or AST) are more than 2.5 times the upper normal limit, or whose bilirubin is more than 1.5 times the upper normal limit, or whose creatine kinase is more than 3 times the upper normal limit, or who have had a significant bleeding or blood clot event
  • People who have previously received an organ transplant or bone marrow/stem cell transplant from another person
  • People with a known allergy or sensitivity to the study drug or any of its ingredients
  • People with any other condition that the trial doctor believes could be harmful or prevent them from completing the study requirements

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 22 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: Jinghui Wang, Director of Research Laboratory, Beijing Chest Hospital

Phone: 13683128239

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
Beijing Chest Hospital, Capital Medical University
Registry
ClinicalTrials.gov
Start date
14 August 2024
Est. completion
1 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

pCR

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: 22 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