Study identifier:16014
ClinicalTrials.gov identifier:NCT02406261
EudraCT identifier:N/A
CTIS identifier:N/A
A Study to Characterize LY3314814 Pharmacokinetics as a Function of Dosing Duration and to Determine the Effect of LY3314814 on the Pharmacokinetics of CYP3A Substrates in Healthy Subjects
Healthy
Phase 1
Yes
Lanabecestat, Simvastatin, Midazolam, Donepezil
All
82
Interventional
18 Years - 65 Years
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Other
Verified 01 Oct 2019 by AstraZeneca
AstraZeneca
Eli Lilly and Company
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Cohort A 500 microgram (mcg) midazolam, single oral dose on Days 1, 17, and 35; 20 mg simvastatin, single oral dose on Days 2 and 36; 250 microgram (mcg) midazolam, intravenous (IV) on Days 3 and 37; 50 mg lanabecestat, single oral dose on Day 4; 50 mg lanabecestat, single oral dose, Days 10 to 37 | Drug: Lanabecestat 50 mg lanabecestat will be administered orally as 1 × 50-mg tablet Other Name: LY3314814 Other Name: AZD3293 Drug: Simvastatin 20 mg simvastatin will be administered orally as 1 × 20-mg tablet Drug: Midazolam 500 mcg midazolam will be administered orally as 0.25 mL of 2-mg/mL syrup Drug: Midazolam 250 mcg midazolam will be administered intravenous (IV) as 0.25 mL of 1-mg/mL injection solution |
Experimental: Cohort B 5 mg donepezil, single oral dose on Day 1, Period 1; 50 mg lanabecestat, single oral dose Days 1 to 43, Period 2; 5 mg donepezil, single oral dose on Day 28, Period 2 | Drug: Donepezil 5 mg donepezil will be administered orally as 1 × 5-mg tablet Drug: Lanabecestat 50 mg lanabecestat will be administered orally as 1 × 50-mg tablet Other Name: LY3314814 Other Name: AZD3293 |