Study identifier:D2600C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Single Centre, Double-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability and Pharmacokinetics of Oral AZD2423 Solution after Multiple Ascending Doses in Young and Elderly Healthy Volunteers
Healthy
Phase 1
Yes
Part 1 - AZD2423 or Placebo, Part 2 - AZD2423, Part 3 - AZD2423
All
74
Interventional
20 Years - 80 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Part 1 AZD2423 or Placebo AZD2423 or Placebo Oral Solution, multiple dosing during 10-14 days | Drug: Part 1 - AZD2423 or Placebo AZD2423 Oral Solution, multiple dosing during 10-14 days or Placebo Oral Solution, multiple dosing during 10-14 days |
Experimental: Part 2 - AZD2423 AZD2423 Oral solution, multiple dosing | Drug: Part 2 - AZD2423 AZD2423 Oral solution, multiple dosing |
Experimental: Part 3 - AZD2423 AZD2423 Oral solution single dosing or AZD2423 Oral solution, single dosing - With Food or AZD2423 Oral solution, single dosing - Fasting Condition. | Drug: Part 3 - AZD2423 AZD2423 Oral solution, single dosing or AZD2423 Oral solution, single dosing - With Food or AZD2423 Oral solution, single dosing - Fasting Condition. |