This study will assess the safety and pharmacokinetic (PK) profile of single ascending doses of CTP-692 in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
42
Collaborative Neuroscience Network, LLC
Long Beach, California, United States
Number of Participants with Adverse Events as a Measure of Safety
Time frame: 48 hours
Measurement of CTP-692 exposure in plasma under fasted conditions
Time frame: 48 hours
Measurement of CTP-692 exposure in plasma under fed conditions
Time frame: 48 hours
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