Japanese single and multiple ascending dose, safety, tolerability, Pharmacokinetic (PK) & Pharmacodynamic (PD) study of AZD7687 - JSMAD

Study identifier:D2710C00004

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase I, Single Centre, Single-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of oral AZD7687 after Administration of Single and Multiple Ascending Doses in Healthy Male Japanese Subjects

Medical condition

Type 2 Diabetes

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD7687

Sex

Male

Actual Enrollment

36

Study type

Interventional

Age

20 Years - 45 Years

Date

Study Start Date: 01 Nov 2010
Primary Completion Date: 01 Jul 2011
Study Completion Date: 01 Jul 2011

Study design

Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Double Blind
Primary Purpose: Basic Science

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria