At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 17 enrolled
Drug / intervention
MK-5720 +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of the Long-Acting Injectable of MK-5720 in Participants With Schizophrenia
In Brief
A Phase 1 clinical trial evaluating MK-5720, Placebo to MK-5720, and 2 other interventions for Schizophrenia. Completed, enrolled 17 participants across 4 sites.
Detailed Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of single ascending intramuscular doses of MK-5720, and the safety and tolerability of multiple once-daily oral doses of MK-8189, in participants with schizophrenia. The primary study hypothesis is that the administration of MK-5720 is safe and well tolerated.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSchizophrenia
CountriesUnited States
Collaborators--
Timeline
Phase 1CompletedFinished
202420252026
First PostedJul 2023
Enrollment StartSep 2023
Primary CompletionFeb 2024
TodayJul 2026
First PostedJul 20, 2023
Enrollment StartSep 15, 2023
Primary CompletionFeb 15, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 2.9 years ago
Interventions
MK-5720drug
IM injection
Placebo to MK-5720drug
Placebo IM Injection matched to MK-5720
MK-8189drug
Oral Tablet
Placebo to MK-8189drug
Placebo oral tablet matched to MK-8189