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COMPLETED
NCT05406440
PHASE1

A Study of Elpipodect (MK-8189) in Participants With Schizophrenia (MK-8189-014)

Sponsor: Merck Sharp & Dohme LLC

View on ClinicalTrials.gov

Summary

The primary purpose of this study is to assess the safety and tolerability of multiple ascending doses of elpipodect in participants with schizophrenia.

Official title: A Multiple Ascending Dose Clinical Study to Evaluate the Safety, Tolerability, PK and the Effect of MK-8189 on QTc in Participants With Schizophrenia

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

53

Start Date

2022-07-12

Completion Date

2023-02-24

Last Updated

2026-04-29

Healthy Volunteers

No

Conditions

Interventions

DRUG

Elpipodect

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.

DRUG

Placebo

MK-8189 dose-matching placebo tablets will be administered orally QD.

Locations (3)

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