Ticagrelor China Pharmacokinetic/Pharmacodynamic study

Study identifier:D5130C00086

ClinicalTrials.gov identifier:NCT02064985

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An Open Label, Single Centre, Randomised, Phase IV, Pharmacokinetic, Pharmacodynamic, and Safety Study to Evaluate Single and Multiple Doses of 45, 60, and 90 mg of Ticagrelor in Chinese Patients with Stable Coronary Heart Disease

Medical condition

stable coronary heart disease (CHD)

Phase

Phase 4

Healthy volunteers

No

Study drug

Inhibition of Platelet Aggregation by "Brilinta"(Ticagrelor)

Sex

All

Actual Enrollment

61

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 01 Feb 2014
Primary Completion Date: 01 Nov 2014
Study Completion Date: 01 Nov 2014

Study design

Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 Jun 2016 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria