Study identifier:D5010C00005
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1, Open-label, Randomized, Single-dose, 3-period Cross-over, Relative Bioavailability Study to Assess Two Solid Formulations Compared to an Oral Solution of AZD3293 in Healthy Male and Non-Fertile Female Subjects
Healthy Volunteers, Pharmacologic action
Phase 1
Yes
AZD3293 oral solution, AZD3293 tablet formulation A, AZD3293 tablet formulation B
All
1
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: Bio-availability Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Apr 2014 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZD3293 oral solution single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15) | Drug: AZD3293 oral solution Subjects will receive AZD3293 as a tablet (Formulation A; Formulation B) and solution as a single dose on Day 1, Day 8 or Day 15. Other Name: Beta secretase inhibitor |
Experimental: AZD3293 tablet formulation A single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15) | Drug: AZD3293 tablet formulation A Subjects will receive AZD3293 as a tablet (Formulation A; Formulation B) and a solution as a single dose on Day 1, Day 8, or Day 15. Other Name: beta secretase inhibitor |
Experimental: AZD3293 tablet formulation B single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15) | Drug: AZD3293 tablet formulation B Subjects will receive AZD3293 as a tablet (Formulation A; Formulation B) and a solution as a single dose on Day 1, Day 8 or Day 15. Other Name: Beta secretase inhibitor |