Overview

A Study of LY2835219 in Participants With Cancer

Status:
Completed
Trial end date:
2015-08-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to assess how the body handles Abemaciclib when it is given with another drug called clarithromycin. The study doctor will measure the amount of Abemaciclib that is absorbed into the blood stream and the time that it takes to remove Abemaciclib from the body. The safety and tolerability of these drugs will be studied. Each participant will complete 2 study periods in fixed order. After screening, Period 1 will last approximately 8 days and Period 2 will last approximately 15 days. Participants who complete Period 2 may continue to receive Abemaciclib in 28-day cycles until discontinuation criteria are met.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Eli Lilly and Company
Treatments:
Clarithromycin
Criteria
Inclusion Criteria:

- Have histological or cytological evidence of cancer (solid tumors) that is advanced
and/or metastatic

- Have a performance status of 0 to 2 on the Eastern Cooperative Oncology Group (ECOG)
scale

Exclusion Criteria:

- No symptomatic central nervous system (CNS) malignancy or metastasis