Overview

A Study of LY3202626 in Healthy Participants and Participants With Alzheimer's Disease

Status:
Completed
Trial end date:
2016-02-01
Target enrollment:
0
Participant gender:
All
Summary
This study involves single and multiple doses of LY3202626 and will evaluate the effects of LY3202626 on the body. There will be 4 parts to this study. In Parts A and B, single increasing doses of LY3202626 will be given in capsule form. Part A will also include itraconazole given orally as a solution. Part A will last approximately 8-12 weeks. Part B will last approximately 5-6 weeks. In Parts C and D, participants will be dosed multiple days with the study drug. Part C will last approximately 11-14 weeks. Part D will last approximately 11-14 weeks and participants must have Alzheimer's Disease. Participants may only enroll in one part.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Eli Lilly and Company
Treatments:
Hydroxyitraconazole
Itraconazole
Criteria
Inclusion Criteria:

- For Parts A, B, and C, are overtly healthy males or females (nonchildbearing
potential), as determined by medical history and physical examination

- Have a body mass index (BMI) of 18 to 32 kilograms per square meter (kg/m^2)

- For Part D, present with Mild Cognitive Impairment (MCI) due to Alzheimer's Disease
(AD) or mild to moderate AD

- Have venous access sufficient to allow for blood sampling

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

Exclusion Criteria:

- Taking over-the-counter or prescription medication with the exception of vitamins or
minerals

- Smoke more than 10 cigarettes per day

- Are unwilling or unable to refrain from eating any food or drinking any beverage
containing grapefruit or grapefruit juice for at least 2 weeks prior to first dose
until completion of the study