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Study of Olomorasib (LY3537982) in Combination With Standard of Care in Participants With Resected or Unresectable KRAS G12C-mutant Non-Small Cell Lung Cancer

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NCT06890598 · readout ≤ 1,015 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →. With AstraZeneca.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
700estimated
Sites
370
Countries
Australia, Austria, Belgium +26

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
Start2025-03-27actualWhen the study began enrolling
Primary completionMay 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2032estimatedThe whole study's end, after follow-up
First posted2025-03-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Carcinoma, Non-Small-Cell Lung

Interventions

  • Drug: Olomorasib — also filed as LY3537982
  • Drug: Pembrolizumab
  • Drug: Durvalumab
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Part A: Disease-Free Survival (DFS) by Investigator Assessment
measured Randomization to disease recurrence or death from any cause (Estimated as approximately 4 years).
Part B: Progression-Free Survival (PFS) by BICR
measured Randomization to disease progression or death from any cause (Estimated as approximately 3 years).

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