Healthy Subjects Clinical Trial
Official title:
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Sequential Group, Multiple-Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ASP015K in Healthy, Non-Elderly Male and Female Adult Volunteers
The objective of this study is to explore safety and tolerability of multiple oral doses of ASP015K in healthy volunteers.
Subjects will be confined to the clinical research unit for 19 days. Subjects will receive a
follow-up phone call to asses safety 1 to 5 days after being discharged from the study.
Subjects will receive study drug twice per day (BID) on days 1 to 13 of the 14 day treatment
period, and will receive a single dose of study drug on the morning of day 14 of the
treatment period.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
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