A Study of LY3295668 Erbumine in Participants With Extensive-stage Small-Cell Lung Cancer
The purpose of this study is to determine the recommended phase 2 dose of LY3295668 erbumine in participants with platinum-sensitive, extensive-stage small-cell lung cancer.
Trial Summary
Key Requirements
Clinical trials have inclusion and exclusion requirements to determine which individuals qualify for participation. Listed below are key requirements for this clinical trial, but there may be additional requirements to qualify.Participants Must:
Participants must have histological or cytological evidence of a diagnosis of platinum sensitive small cell lung cancer that is extensive stage
Participants must have adequate organ function
Participants must have a performance status (PS) of 1 on the Eastern Cooperative Oncology Group (ECOG) scale
Participants must have discontinued previous treatments for cancer.
Participants must be able to swallow capsules
Participants Must Not:
Participants must not be currently enrolled in a clinical study
Participants must not have a serious concomitant systemic disorder
Participants must not have a symptomatic human immunodeficiency virus infection or symptomatic activated/reactivated hepatitis B or C
Participants must not have a significant cardiac condition
Participants must not have previously received an aurora kinase inhibitor
Lilly Trial Alerts
You will complete the questionnaire on another website.YesNo