Healthy Subjects Clinical Trial
Official title:
A Double-blind, Randomized, Placebo-controlled Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Ascending Multiple Oral Doses of ASP3652 in Healthy Young and Elderly Male and Female Subjects
The study investigates how safe ASP3652 is and how well it is tolerated when taken as
multiple doses. The study also assesses how quickly and to what extent it is absorbed and
eliminated from the body. In addition, the effects of age and gender are investigated.
The study consists of two parts. In Part 1 four dose levels are administered to four
separate groups initially. Two additional dosages are then investigated. Subjects receive
either a once-daily dose (QD) or twice-daily dose (BID) of ASP3652 or placebo.
Part 2 is performed in one group of elderly healthy male or female (post-menopausal)
subjects. Subjects receive either a twice daily dose (BID) of ASP3652 or placebo.
For both parts of the study, the subjects stay in the clinic for one period of 18 days.
This is a Multiple Ascending Dose (MAD) study with two parts. Screening for both parts takes
place between Days -28 and -3. Subjects are admitted to the clinic on Day -2, and discharged
on Day 16. They return for an End of Study Visit (ESV) between 7 and 14 days after (early)
discharge.
Part 1 evaluates the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD)
of ASP3652 following ascending multiple oral doses. The initially planned four dose levels
or matching placebo are given to four separate groups. Thereafter two additional dosage
levels are further investigated. All groups receive a single dose of ASP3652 administered in
the morning of Day 1 and Day 14, and twice-daily doses administered from Day 2 to Day 13
under fasted conditions, except the last group which receives all dosages once daily from
Day 1 to Day 14.
Part 2 evaluates the safety, tolerability, PK and PD of ASP3652 following ascending multiple
oral doses in healthy elderly male and female subjects. This part contains a single,
placebo-controlled group. All subjects receive twice daily doses and administration is based
on the results of Part 1.
All subjects in both parts receive training for Neurocognitive Test Battery (NTB) and tests
for monitoring of psychotropic effects.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Basic Science
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