A Study of LY3023414 in Participants With Advanced Cancer
The purpose of this study is to find a recommended dose level and schedule of dosing LY3023414 that can safely be taken by participants with advanced or metastatic cancer. The study will also explore the changes to various markers in blood cells and potentially tumor cells. Finally, the study will help document any antitumor activity this drug may have.
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:
Participant in part B4 must have malignant pleural or peritoneal mesothelioma and appropriate candidate for treatment with cisplatin/pemetrexed; no prior systemic chemotherapy
Participant in part B6 must have squamous NSCLC; documented evidence of an activating molecular aberration of the PI3K/mTOR pathway
Participant in part B7 must have HR+ abd HER2- breast cancer
Participant may need to undergo a biopsy dependent upon which arm of the study you are in
Participant must be able to swallow capsules
Participant must be reliable and willing to make themselves available for the duration of the study and be willing to follow study procedures
Participants Must Not:
Participant must not have known acute or chronic leukemia
Participant must not have insulin-dependent diabetes mellitus or a history of gestational diabetes mellitus
Lilly Trial Alerts
You will complete the questionnaire on another website.YesNo