Study of the Effect of Single Doses of MK2637 and Dextromethorphan on Cerebral Cortex Excitability (2637-008)

NCT ID: NCT00934466

Last Updated: 2015-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-07-31

Study Completion Date

2009-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will assess transcranial magnetic stimulation (TMS) as a biomarker and characterize TMS readouts of the activity of MK2637 and dextromethorphan. Resting quantitative electroencephalography(qEEG) readouts are also characterized with MK2637 and dextromethorphan.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Schizophrenia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

MK2637 120 mg

Group Type EXPERIMENTAL

MK2637

Intervention Type DRUG

Single dose of 120 mg MK2637 capsules in one of five treatment periods.

2

MK2637 50 mg

Group Type EXPERIMENTAL

Comparator: MK2637

Intervention Type DRUG

Single dose of 50 mg MK2637 capsules in one of five treatment periods.

3

Placebo

Group Type PLACEBO_COMPARATOR

Comparator: Placebo

Intervention Type DRUG

Single dose of placebo only in one of five treatment periods.

4

Dextromethorphan 220 mg

Group Type ACTIVE_COMPARATOR

Comparator: Dextromethorphan

Intervention Type DRUG

Single dose of 220 mg dextromethorphan capsules in one of five treatment periods.

5

Dextromethorphan 110 mg

Group Type ACTIVE_COMPARATOR

Comparator: Dextromethorphan

Intervention Type DRUG

Single dose of 110 mg dextromethorphan capsules in one of five treatment periods.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

MK2637

Single dose of 120 mg MK2637 capsules in one of five treatment periods.

Intervention Type DRUG

Comparator: MK2637

Single dose of 50 mg MK2637 capsules in one of five treatment periods.

Intervention Type DRUG

Comparator: Placebo

Single dose of placebo only in one of five treatment periods.

Intervention Type DRUG

Comparator: Dextromethorphan

Single dose of 220 mg dextromethorphan capsules in one of five treatment periods.

Intervention Type DRUG

Comparator: Dextromethorphan

Single dose of 110 mg dextromethorphan capsules in one of five treatment periods.

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Subject is right-handed
* Subject is in good health
* Subject is a nonsmoker

Exclusion Criteria

* Subject works a night shift
* Subject has a history of any illness that might make participation in the study unsafe or confound the study results
* Subject has a history of head injury
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Medical Monitor

Role: STUDY_DIRECTOR

Merck Sharp & Dohme LLC

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MK2637-008

Identifier Type: -

Identifier Source: secondary_id

2009_608

Identifier Type: -

Identifier Source: secondary_id

2637-008

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Treatment of Negative Symptoms and Schizophrenia
NCT02204787 COMPLETED PHASE1/PHASE2
Externalization and Stimulation
NCT05936307 UNKNOWN NA
Trial of D-Cycloserine in Schizophrenia
NCT00000371 COMPLETED PHASE3