Imzokitug with Pumitamig for Non-Small Cell Lung Cancer
A Study To Assess the Safety, Tolerability, and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment for Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 160 (estimated)
- Sponsor
- Bristol-Myers Squibb · Industry
This trial is looking for adults with advanced lung cancer who have not received prior chemotherapy for their cancer. Participants will receive Imzokitug along with other treatments to see how well it works and what side effects it may have.
You may be able to join if
- I have stage IV non-small cell lung cancer.
- I have not received prior treatment for my advanced cancer.
- I have a sample of my tumor tissue available.
- I have a performance status of 0 or 1.
- I have measurable disease.
You may not be able to join if
- I have actionable genomic alterations that need targeted therapy.
- I have previously received immuno-oncology therapies.
- I have untreated central nervous system metastases.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your EligibilityThe purpose of this study is to assess the safety, tolerability, and efficacy of Imzokitug in combination with Pumitamig and Platinum-Doublet Chemotherapy (PDCT) versus Pumitamig and PDCT as first-line treatment for participants with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)
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BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
855-907-3286
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