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Completed

NCT Number: NCT06273774

A Study of Elpipodect (MK-8189) in Participants With Bipolar I Disorder (MK-8189-020)

The goal of this study is to evaluate the safety and tolerability of elpipodect in participants with stable bipolar I disorder. There was no hypothesis testing in this study.

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Key information

Conditions

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Woodland International Research Group-Clinical Research ( Site 0009), Little Rock, Arkansas, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

The main inclusion criteria include but are not limited to the following:

  • Meets diagnostic criteria for bipolar I disorder, manic or mixed features according to the Diagnostic and statistical manual of Mental Disorders TR (DSM-5 TR) and considered to be in a non-acute phase of their illness.
  • History of receiving and tolerating antipsychotic medication within the usual dose range employed for bipolar I disorder.
  • Body mass index is 18 and 40 kg/m^2, inclusive.
  • If currently taking an antipsychotic, is able to discontinue use at least 5 days prior to study start and the duration of the study.

Exclusion criteria

The main exclusion criteria include but are not limited to the following:

  • Untreated or uncompensated endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological abnormalities or diseases.
  • Evidence or history of a primary DSM-5 axis I psychiatric diagnosis other than those specified for inclusion.
  • History of cancer (malignancy).
  • Evidence or history of mental retardation, borderline personality disorder, or organic brain syndrome.
  • History of neuroleptic malignant syndrome or moderate to severe tardive dyskinesia.
  • Substance-induced psychotic disorder or behavioral disturbance.
  • DSM-5 TR defined substance use disorder within 3 months of screening.
  • History of seizure disorder beyond childhood or is receiving treatment with any anticonvulsant to prevent seizures.
  • Positive test(s) for hepatitis B surface antigen, hepatitis C antibodies or human immunodeficiency virus.
  • Major surgery or donation/loss of 1 unit of blood within 4 weeks prior to screening.
  • Received any vaccine starting from 30 days prior to study intervention or is scheduled to receive any vaccine through 30 days following study intervention.

Treatment and study plan

Elpipodect

Drug

Oral Tablet

Other names: MK-8189

Placebo

Drug

Oral Tablet

Primary outcomes

  1. Number of Participants Who Experience One or More Adverse Events (AEs)

    Time frame: Up to 28 days

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.

  2. Number of Participants Who Discontinue Study Treatment Due to an AE

    Time frame: Up to 14 days

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.

Sponsors and collaborators

Lead sponsor

Merck Sharp & Dohme LLC

Industry

Registry information

Official study title

A Multiple Dose Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of MK-8189 in Participants With Bipolar I Disorder

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Feb 23, 2024
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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