This study will assess in healthy male and female subjects the safety, tolerability and pharmacokinetics (PK) profiles of Immediate Release CTP-730 at steady state following 7 days of dosing. Three doses of Immediate Release (IR) CTP-730 capsules will be studied.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
30
CMAX
Adelaide, South Australia, Australia
Pharmacokinetic Profile
The primary pharmacokinetics parameters of interest will be time to attainment of steady state, and Cmax, Tmax, AUC0-24hr, AUClast and AUCinf at steady state
Time frame: 96 hours
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Adverse events categorized by body system and MedDRA term
Time frame: 24 hours
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