Overview

A Study of LY3154207 in Healthy Participants and Participants With Parkinson's Disease

Status:
Completed
Trial end date:
2017-03-03
Target enrollment:
0
Participant gender:
All
Summary
This two-part study will evaluate how safe LY3154207 is and the effects it has on the body. Part A will include healthy participants. Each participant will receive daily doses of LY3154207 or placebo for 14 days. Part A will last approximately 4 weeks including a 17 day stay in the clinical research unit (CRU) and follow-up. Part B is contingent on the results of Part A. Part B will include participants with Parkinson's disease. Each participant will receive daily doses of LY3154207 or placebo for 14 days. Part B will last approximately 4 weeks including a 17 day stay in the CRU and follow-up. Both Part A and Part B will require screening within 30 days prior to the start of the study.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Eli Lilly and Company
Criteria
Inclusion Criteria:

Part A:

- Overtly healthy males or females, as determined by medical history and physical
examination

- Female participants not of child-bearing potential

Part B:

- Have a clinical diagnosis of idiopathic Parkinson's disease for at least 1 year and on
stable medication for at least 4 weeks

Part A and B

- Are reliable and willing to make themselves available for the duration of the study
and are willing to follow study procedures

- Have given written informed consent

- Have a body mass index (BMI) of 18.0 to 29.9 kilograms per square meter (kg/m²)

Exclusion Criteria:

- Have participated, in the last 30 days, in a clinical trial involving an
investigational product

- Have a significant history of or current cardiovascular, respiratory, hepatic, renal,
gastrointestinal, endocrine, hematological or neurological disorders capable of
significantly altering the absorption, metabolism or elimination of drugs; or
constituting a risk when taking the study medication; or interfering with the
interpretation of study data