Pharmacokinetics Clinical Trial
Official title:
An Open-label, Randomized, Three-period, Three-treatment, Crossover, Single-centre, Single-dose Study to Assess the Bioequivalence Between Ticagrelor Orodispersible Tablets and Ticagrelor Immediate-release Tablets in Healthy Japanese Subjects.
This study will be an open-label, randomised, three-period, three-treatment, crossover study
in healthy Japanese male and female of non-childbearing potential subjects, performed at a
single study centre.
The objective of the study is to assess the bioequivalence of ticagrelor orodispersible (OD)
tablets when administered with water and without water and ticagrelor immediate-release (IR)
tablets.
Study to evaluate the bioequivalence of ticagrelor orodispersible (OD) tablets administered with water and without water and ticagrelor immediate-release (IR) tablets. ;
Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science
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