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Real-World Outcomes of First-Line Nivolumab + Ipilimumab With Chemotherapy in Non-Small Cell Lung Cancer in Poland

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NCT07526961

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
240actual
Sites
1
Country
Poland

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-12-01actualWhen the study began enrolling
Primary completion2026-01-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-20actualThe whole study's end, after follow-up
First posted2026-04-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-14actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Non-Small Cell Lung Cancer

Intervention

  • Combination product: Nivolumab + Ipilimumab + Chemotherapy

Primary outcomes

what the primary-completion date above is the date OF
Second-line systemic anticancer treatment prescribed after progression/discontinuation of first-line therapy
measured Up to 26 months
Third-line systemic anticancer treatment prescribed after progression/discontinuation of second-line therapy
measured Up to 26 months
Overall Response Rate (ORR) Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
measured Up to 26 months
Disease Control Rate (DCR) Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
measured Up to 26 months
Progression-Free Survival (PFS)
measured Up to 26 months
Duration of Response (DOR) Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
measured Up to 26 months
Overall Survival (OS)
measured Up to 26 months
Duration of Treatment
measured Up to 26 months

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