Long-term Outcomes Among Patients With Programmed Death-ligand 1 <1% Metastatic Non-small Cell Lung Cancer Treated With First-line Nivolumab + Ipilimumab + 2 Cycles of Chemotherapy
Running, not enrolling
Conditions studied: Metastatic Non-small Cell Lung Cancer
In brief
The study will assess the long-term real-world outcomes among adults diagnosed with programmed death-ligand 1 (PD-L1) \<1% metastatic non-small cell lung cancer (mNSCLC) treated with first-line (1L) nivolumab + ipilimumab + 2 cycles of chemotherapy (NIC) in the US
Key facts
- Study ID
- NCT07024862
- Run by
- Bristol-Myers Squibb
- People needed
- 100
- Starts
- 2024-10-24
- Expected to finish
- 2025-06-30
- Last updated by the study team
- 2025-06-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- At least 18 years old at confirmed diagnosis with metastatic non-small cell lung cancer (NSCLC) (stage IV), squamous or non-squamous histology
- Initiated first-line (1L) combination nivolumab, ipilimumab, and 2 cycles of platinum-doublet chemotherapy (NIC) regimen between 01 January 2018 and 2 years prior to study launch
- Tumor programmed death-ligand 1 (PD-L1) negative expression (i.e., PD-L1 <1%)
- No EGFR, ALK, or ROS1 genetic mutation (i.e., wild type)
- Minimum of 6 months of follow-up after initiation of 1L NIC*
You may not qualify if…
- Any prior systemic therapy for metastatic non-small cell lung cancer (NSCLC)
Where it is running
- Cardinal Health — Dublin, Ohio, United States
Full record on ClinicalTrials.gov
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