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
← catalyst calendarNCT06269133 · 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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-02-21 | actual | When the study began enrolling |
| Primary completion | 2027-03-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-06-23 | estimated | The whole study's end, after follow-up |
| First posted | 2024-02-21 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-08 | actual | The 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 OFReal-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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