Phase 2 Lung Cancer Trial, Recruiting NCT07122687 Sponsor: Innovent Biologics (Suzhou) Co. Ltd. Condition: Lung Cancer
Back to Lung Cancer

Phase 2 Lung Cancer Trial, Recruiting

NCT07122687
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:

  • Adults aged 18 to 75 years (male or female)
  • People with a laboratory-confirmed diagnosis of a specific type of lung cancer called non-squamous non-small cell lung cancer (NSCLC), at stages IB, II, IIIA, or IIIB (N2)
  • People who have not received any treatment for their lung cancer before surgery
  • People whose cancer can be removed with surgery, and whose lung function is strong enough to tolerate that surgery
  • People whose cancer does not have specific gene changes known as EGFR mutations or ALK translocation
  • People who have at least one measurable tumour, as assessed by standard imaging criteria
  • People with a good general level of physical functioning (rated 0 or 1 on a standard medical scale, meaning fully active or able to carry out light activity)
  • People with adequate organ function confirmed through screening tests

Who may not be able to join:

  • People whose lung cancer is confirmed to be small cell lung cancer, or certain other tumour types including neuroendocrine carcinoma, sarcoma, salivary gland tumour, mesenchymal tumour, or a mixed type with mainly squamous cell features
  • People whose tumour has grown into nearby important structures and is causing symptoms or requiring medical treatment
  • People with a type of tumour located at the top of the lung called a Pancoast tumour
  • People who have a cancerous tumour nodule in the opposite lung
  • People with known or suspected cancer spread to the brain or other distant parts of the body
  • People who have used Chinese herbal medicines, traditional Chinese medicinal products with anti-tumour properties, or immune-modifying drugs within 2 weeks before the first study treatment
  • People who need ongoing steroid treatment throughout the body, or who have received other immune-suppressing therapy within 7 days before the first study treatment
  • People who have had a blood clot in an artery within the 6 months before the first study treatment
  • People who have had a blood clot in a deep vein, a clot in the lungs, or another serious blood clot in a vein within 3 months before the first study treatment
  • People with a history of lung inflammation (pneumonitis) that required steroid treatment, or significant lung disease (or suspected lung disease seen on imaging during screening)
  • People with active or uncontrolled medical conditions (confirm with trial site)
  • People with a history of immune deficiency disease
  • People who have had an active autoimmune disease requiring treatment throughout the body at any point in the 2 years before the first study treatment

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

Phone: 15005136320

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
Innovent Biologics (Suzhou) Co. Ltd.
Registry
ClinicalTrials.gov
Start date
26 August 2025
Est. completion
30 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathologic Complete Response (pCR) rate; Safety parameters: the incidence of all adverse events (AEs); Safety parameters: the incidence of treatment-emergent adverse events (TEAEs); Safety parameters: the incidence of immune-related adverse events (irAEs); Safety parameters: the incidence of adverse events of special interest (AESIs); Safety parameters: the incidence of serious adverse events (SAE); Safety parameters: the relatedness of infusion-related reactions (IRRs) to the investigational product and their severity; Safety parameters: the surgery delay rate; Proportion of subjects with abn...

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