The primary purpose of this study is to assess the safety and tolerability of multiple ascending doses of elpipodect in participants with schizophrenia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
53
MK-8189 4 mg and/or 12 mg tablet(s) will be administered orally QD for a total daily dose of 48 mg, 60 mg, 80 mg.
MK-8189 dose-matching placebo tablets will be administered orally QD.
Collaborative Neuroscience Research, LLC ( Site 0004)
Garden Grove, California, United States
California Clinical Trials Medical Group managed by PAREXEL ( Site 0002)
Glendale, California, United States
Hassman Research Institute Marlton Site ( Site 0003)
Marlton, New Jersey, United States
Number of Participants Experiencing an Adverse Event (AE)
An AE is any untoward medical occurrence in a clinical study participant, temporarily associated with the use of study intervention, whether or not considered related to the study intervention. The number of participants who experienced one or more AEs were reported.
Time frame: Up to approximately 17 days
Number of Participants Who Discontinue From Study Treatment Due to an AE
An AE is any untoward medical occurrence in a clinical study participant, temporarily associated with the use of study intervention, whether or not considered related to the study intervention. The number of participants who discontinued study due to an AE were reported.
Time frame: Up to approximately 3 days
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