Phase 2 Lung Cancer Trial, Recruiting NCT07325136 Sponsor: Bristol-Myers Squibb Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT07325136
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 with small cell lung cancer that has come back or stopped responding to treatment, confirmed through a laboratory test on a tissue or cell sample.
  • People who have already received at least one chemotherapy treatment that included a platinum-based drug, as approved in their country and following their hospital's guidelines.
  • In countries where the standard first-line treatment includes platinum chemotherapy combined with an anti-PD-(L)1 therapy (a type of immunotherapy), people whose cancer has grown despite that treatment, or for whom that immunotherapy was not an option or was not available to them.

Who may not be able to join:

  • People who have cancer that has spread to the brain or spinal cord and has not yet been treated.
  • People who have an active autoimmune disease, or a condition that is known or suspected to involve the immune system attacking the body.
  • People who have previously received an organ or tissue transplant from another person.
  • There are additional criteria set out in the study protocol that may also affect eligibility (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 23 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: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

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
Registry
ClinicalTrials.gov
Start date
3 February 2026
Est. completion
23 April 2029

Where this trial is recruiting

🇨🇳 China 🇮🇹 Italy 🇯🇵 Japan 🇷🇴 Romania 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Number of participants with adverse events (AEs); Number of participants with serious adverse events (SAEs); Number of participants with AEs meeting dose-limiting toxicity (DLT) criteria; Number of participants with AEs leading to discontinuation; Number of participants with AEs leading to death

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: 23 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