Healthy Subjects Clinical Trial
Official title:
A Phase I, Double Blind, Placebo-controlled, Randomized 4-way Alternating Cross-over Study to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effects of Single Ascending Doses of ASP3652 in Healthy Young Caucasian Male and Female Subjects
The purpose of this study is to explore the safety (including the effect on cardiac intervals), tolerability, the effects on the Central Nervous System (CNS), as well as the CNS side effect profile of single ascending doses of ASP3652 in healthy, Caucasian male and female subjects.
Each subject receives 3 single ascending doses of ASP3652 and a single dose of matching
placebo during one randomly selected investigational period. Randomization is conducted
separately for males and females.
The washout period between dosing occasions is at least 7 days. Screening takes place from
Day -22 to Day -2. Subjects are admitted to the clinic in the afternoon of Day -1 of
investigational period 1, 2, 3 and 4 for pre-dose assessments.
On Day -1 of all investigational periods, subjects do not take any food or drink for at
least 10 hours before the anticipated dosing time on Day 1. For the duration of their stay
in the clinic, subjects are not allowed to consume caffeine or other xanthine-containing
drinks.
The subjects are discharged on Day 4 of each investigational period. The End of Study Visit
(ESV) is planned to take place 7-14 days after early discharge or after Day 4 of
investigational period 4.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science
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