Phase 2 Lung Cancer Trial, Recruiting NCT07227298 Sponsor: Pfizer Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07227298
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 have been diagnosed through laboratory testing with locally advanced (Stage IIIB or IIIC) or metastatic (Stage IV) non-small cell lung cancer (NSCLC) — either squamous or non-squamous type — where surgery to fully remove the cancer and curative radiation/chemotherapy combined treatment are not suitable options
  • People whose cancer has been tested for a marker called PD-L1, with results available
  • People in Part B of the trial only: those whose PD-L1 test result shows a score of 1% or higher
  • People whose cancer has at least one measurable area that can be tracked using standard imaging guidelines
  • People who are in relatively good general health, able to carry out normal daily activities with little or no limitation (scored 0 or 1 on a standard health scale used in cancer trials)
  • People whose liver, kidneys, and other organs are functioning well enough to meet the trial's health requirements

Who may not be able to join:

  • People whose cancer has certain known genetic mutations or changes — specifically in genes called EGFR, ALK, ROS1, NTRK, BRAF, or MET
  • People who have had another cancer diagnosed within the past 3 years, or who still show signs of a previously diagnosed cancer
  • People with known active cancer spread to the brain, brainstem, spinal cord, or the membranes surrounding the brain or spinal cord
  • People with a condition called leptomeningeal disease, where cancer has spread to the fluid and membranes surrounding the brain and spinal cord
  • People who have an active autoimmune disease (where the immune system attacks the body) that has required ongoing medical treatment within the past 2 years
  • People who have previously received systemic (whole-body) treatment for locally advanced, unresectable, or metastatic NSCLC
  • People who have previously received immunotherapy (with the exception of certain early-stage preventive immunotherapy treatments), a specific type of antibody-drug therapy containing a payload called MMAE, systemic anti-blood vessel growth therapy, or radiation treatment to the lung within 6 months before joining the trial

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 13 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: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

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
Registry
ClinicalTrials.gov
Start date
30 January 2026
Est. completion
8 March 2029

Where this trial is recruiting

🇨🇳 China 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇯🇵 Japan Puerto Rico 🇪🇸 Spain 🇹🇼 Taiwan 🇺🇸 United States

Primary endpoints

Number of Participants with Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs); Phase I: Number of participants with dose limiting toxicity (DLT); Phase 2: Confirmed Objective Response Rate (ORR) per RECIST v1.1 by investigator

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: 13 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