Phase 3 Lung Cancer Trial, Recruiting NCT06123754 Sponsor: 3D Medicines (Sichuan) Co., Ltd. Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT06123754
Recruiting Phase 3

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 willing to take part and sign a consent form agreeing to participate.
  • People aged 18 or older, of any gender.
  • People who have been diagnosed with a specific type of lung cancer (non-small cell lung cancer, or NSCLC) at stage IIIA or IIIB (with spread to nearby lymph nodes, known as N2), confirmed by laboratory tissue or cell testing, and where surgery to remove the tumour is considered possible.
  • People whose cancer has at least one area that can be measured on scans using a standard set of medical guidelines (RECIST 1.1).
  • People who are generally well enough to carry out light activity and care for themselves, as rated on a standard health scale (ECOG score of 0 or 1).
  • People who are able to provide a tumour tissue sample so that a specific protein (PD-L1) can be tested.
  • People whose liver, kidneys, bone marrow, and other organs are functioning well enough to meet the trial's requirements.
  • People who are expected to live for at least 6 months.
  • People whose overall lung function has been assessed by a surgeon as strong enough to safely undergo the planned lung surgery.

Who may not be able to join:

  • People whose cancer has been confirmed to include certain specific types of tumour cells, such as neuroendocrine, sarcomatous/sarcomatoid, adenosquamous, or other special tissue types.
  • People who have previously been treated with a drug that targets certain parts of the immune system known as T cell receptors (for example, drugs targeting CTLA-4 or OX-40).
  • People who are known to have specific gene changes (EGFR mutation or ALK translocation) in their cancer; and people with non-squamous cell lung cancer whose EGFR and ALK status has not yet been tested.
  • People whose tumour is located at the top of the lung (upper lung sulcus tumour), or whose cancer cannot be surgically removed, or has spread to other parts of the body.
  • People who have already received any previous treatment aimed at this cancer.
  • People with known or suspected lung inflammation (interstitial pneumonia), radiation-related lung damage, or other moderate to severe lung conditions that could interfere with detecting or managing drug-related lung side effects or seriously affect breathing.
  • People who have a serious active infection at the time of joining.
  • People with heart or brain blood vessel disease that is not well controlled or is considered significant.
  • People with an active autoimmune disease (where the immune system attacks the body) that currently requires ongoing medical treatment.
  • People who have taken immune-suppressing medications or steroid medications at a dose above a certain level (more than 10 mg per day of prednisone or equivalent) within the 14 days before being assigned to a treatment group.

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 14 July 2026
Phase 3: approximately ~65% 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: Changli Wang, Tianjin Cancer Hospital

Phone: 0086-22-2340123

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 3
Sponsor
3D Medicines (Sichuan) Co., Ltd.
Registry
ClinicalTrials.gov
Start date
17 November 2023
Est. completion
30 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

MPR by BIPR; EFS by BIRC

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: 14 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