Phase 2 Lung Cancer Trial, Recruiting NCT07120282 Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07120282
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 are able to give written consent and agree to follow the study schedule and requirements
  • People aged 18 years or older
  • People who have been diagnosed with stage I non-small cell lung cancer (confirmed by tissue testing under AJCC 9th edition guidelines), with a tumour measuring between 2cm and 4cm
  • People whose post-surgery pathology report shows at least one higher-risk feature, such as cancer spreading into the lining around the lung, into blood or lymph vessels, through airspaces, or showing poorly differentiated or high-grade patterns
  • People with a general health and activity level rated as fully active or with minor restrictions (ECOG 0 or 1)
  • People whose tumour tests positive for a protein called PD-L1 at 1% or more
  • People whose tumour does not carry certain gene changes known as EGFR or ALK sensitive mutations
  • People who had a complete surgical removal of the tumour with no cancer left behind (called R0 resection)
  • People who are within 8 weeks of surgery and have fully recovered from the operation
  • People whose liver, kidneys, blood, and other organs are functioning adequately

Who may not be able to join:

  • People who have already received any treatment for their current lung cancer, including radiotherapy, chemotherapy, immunotherapy, targeted therapy, or anti-angiogenesis therapy
  • People who have previously had radiotherapy to the chest area, including the lung, oesophagus, middle chest, or breast
  • People whose lung cancer is of a specific subtype called large-cell neuroendocrine carcinoma, or a mixed type that includes small-cell components
  • People whose tumour carries EGFR or ALK sensitive mutations
  • People who had only a smaller-scale lung surgery called a segmentectomy or wedge resection (rather than a larger lobe removal)
  • People whose tumour involves the main airway tubes, or who have a collapsed or blocked lung related to the tumour
  • People with an active autoimmune disease, or a history of an autoimmune disease that has come back
  • People with a history of scarring or inflammation of the lung tissue (interstitial lung disease), including cases caused by drugs or previous radiation that required hormone treatment, or who currently have this condition
  • People who have needed corticosteroid medicines above a certain dose (more than 10mg per day of prednisone or equivalent) or other immune-suppressing medicines within 14 days before being assigned to a study group
  • People who have used certain immune-modifying medicines (such as interferon or interleukin-2) within 4 weeks before the first study dose
  • People who have used herbal medicines intended to control cancer within 14 days before the first study dose
  • People who have received a live or weakened vaccine within 4 weeks before joining, or who plan to receive one during the study or within 5 months after the last dose of the study drug
  • People with a significant history of serious illness or conditions affecting the function of major organs or body systems, as judged by the study doctor
  • People who have had a severe ongoing or active infection requiring systemic antibiotic, antifungal, or antiviral treatment (such as tuberculosis) within 14 days before the first study dose
  • People known to have HIV infection
  • People who have had an organ or stem cell transplant from another person
  • People who have had another active cancer within the 2 years before joining, with some exceptions for certain early-stage or fully treated skin cancers, superficial bladder cancer, or pre-invasive cancers (confirm with trial site)
  • People with certain personal circumstances, or alcohol or drug dependence, that may affect how the study drug is given, how results are interpreted, or that may increase health risks
  • People who are pregnant or breastfeeding, or men and women who plan to try to conceive during the study
  • People currently taking part in another interventional clinical trial (observational studies or follow-up-only study phases may be acceptable — confirm with 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 7 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

Phone: +86 134 3945 7872

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
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Registry
ClinicalTrials.gov
Start date
28 October 2025
Est. completion
15 August 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2 year disease-free survival rate, 2y-DFS 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: 7 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