This study will assess the pharmacokinetics, safety, and tolerability of icalcaprant administered orally in healthy adult Japanese and Han Chinese participants.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
16
Oral capsules
Anaheim Clinical Trials, LLC /ID# 271323
Anaheim, California, United States
Maximum Observed Plasma Concentration (Cmax) of Icalcaprant
Cmax of Icalcaprant
Time frame: Up to approximately 6 days
Time to Cmax (Tmax) of Icalcaprant
Tmax of Icalcaprant
Time frame: Up to approximately 6 days
Terminal Phase Elimination Rate Constant (Beta) of Icalcaprant
Beta of Icalcaprant
Time frame: Up to approximately 6 days
Terminal Phase Elimination Half-Life (t1/2) of Icalcaprant
T1/2 of Icalcaprant
Time frame: Up to approximately 6 days
Area under the plasma concentration-time curve from time 0 until the last measurable Concentration (AUCt) of Icalcaprant
AUCt of Icalcaprant
Time frame: Up to approximately 6 days
Area under the plasma concentration-time curve from time 0 to infinity (AUCinf) of Icalcaprant
AUCinf of Icalcaprant
Time frame: Up to approximately 6 days
Number of Participants with Adverse Events (AEs)
An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. The investigator assesses the relationship of each event to the use of study
Time frame: Up to approximately 37 days
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