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Evaluation of Cemiplimab in Combination With Platinum-Doublet Chemotherapy in First-Line (1L) Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC) in Adult United States (US) Patients

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NCT06269133 · readout in 224 d

Sponsored by Regeneron Pharmaceuticals (industry) · REGN — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
1,000estimated
Sites
1
Country
United States

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
Start2024-02-21actualWhen the study began enrolling
Primary completion2027-03-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-06-23estimatedThe whole study's end, after follow-up
First posted2024-02-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Non-small Cell Lung Cancer

Interventions

  • Drug: REGN2810 — also filed as LIBTAYO®, cemiplimab
  • Other: Platinum-doublet chemotherapy

Primary outcomes

what the primary-completion date above is the date OF
Real-world response rate (rwRR)
measured Approximately 3 years
Any treatment-emergent immune-mediated adverse event (imAE)
measured Approximately 3 years
Any treatment-emergent imAE resulting in hospitalization
measured Approximately 3 years
Any treatment-emergent imAE resulting in death
measured Approximately 3 years
Specific treatment-emergent imAEs
measured Approximately 3 years

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