PIPELINE > TRIAL OVERVIEW

Pan-KRAS Inhibitor
LY4066434
Phase
1
Enrolling

A Phase 1a/1b Study of the Pan-KRAS Inhibitor LY4066434 in Participants With KRAS Mutant Solid Tumorsa 


NCT06607185 show modal icon
Key Inclusion Criteria
  • Histological or cytologically proven diagnosis of locally advanced, unresectable, and/or metastatic solid tumor cancer
  • Have evidence of KRAS G12C, G12D, G12V, G12A, G12S, or G13D mutation in tumor tissue or circulating tumor DNA
  • Have measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1)
  • Have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1
  • Must be able to swallow tablets
  • Select cohorts must have received ≥1 prior line of systemic chemotherapy for advanced or metastatic disease
Key Exclusion Criteria
  • Have known active central nervous system (CNS) metastases and/or carcinomatous meningitis
    • Participants with asymptomatic or treated CNS disease may be eligible
  • Have unresolved toxicities from prior therapy greater than National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v5.0 Grade 1 at the time of starting trial treatment, except for alopecia, peripheral neuropathy, and ongoing endocrinopathies controlled on appropriate replacement therapy
  • Have significant cardiovascular disease defined as unstable angina or acute coronary syndrome, history of myocardial infarction, known reduced left ventricular ejection fraction or heart failure, uncontrolled or symptomatic arrhythmias
  • Have known active hepatitis B, hepatitis C, or untreated HIV
  • Have active uncontrolled systemic bacterial, viral, fungal, or parasitic infection
  • Have other active malignancies unless in remission with life expectancy >2 years
  • Have history of non-infectious pneumonitis/interstitial lung disease (ILD) that required steroids or has current clinically significant pneumonitis/ILD
a

This clinical trial is currently being conducted in the United States and Japan.​

b

Administered orally.​

c

Administered intravenously.​

For information on trial enrollment, locations, and more, call 1-800-545-5979.