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KaRAnaSa Lung cancer
A Phase 1/2 study of amivantamab in combination with olomorasib in patients with metastatic NSCLC
Phase
Compound
Amivantamab (EGFR × MET bispecific Ab) + olomorasib
NCT identifier
NCT07227025
Enrollment

N=~60

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Study overview & design

Key eligibility criteria*:

  • Metastatic NSCLC
  • KRAS G12C mutation
  • KRAS inhibitor naive
  • Progression on or after platinum-based chemo and PD-1 inhibitor
  • Other driver mutations excluded
Study design
Study design

Primary outcomes:

  • Phase 1: Safety
  • Phase 1: DLTs
  • Phase 2: ORR

Secondary outcomes:

  • Safety
  • Phase 2: DOR
  • Phase 2: DCR
  • Phase 2: PFS
  • Phase 2: OS

*Not a complete list of inclusion and exclusion criteria. Not a complete list of outcomes.
DLT, dose-limiting toxicity; DCR, disease control rate; DOR, duration of response; KRAS, Kirsten rat sarcoma; NSCLC, non–small cell lung cancer; ORR, objective response rate; OS, overall survival; PD-1, programmed cell death 1; PFS, progression-free survival; RPC2D, recommended Phase 2 combination dose.

Recruiting site locations
World Map
Canada, China, South Korea, United States
Study design
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Lung biomarkers animation
Biomarkers in lung cancer
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