Dose Ranging Study in Healthy Methadone Maintenance Subjects

NCT ID: NCT00387491

Last Updated: 2019-11-25

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

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-06-30

Study Completion Date

2006-10-31

Brief Summary

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To assess the effect of a single oral dose of MOA-728, an investigational drug, on the oral-cecal transit time in subjects who are taking methadone.

Detailed Description

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Conditions

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Adult

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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MOA-728

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Men or nonlactating and nonpregnant women, aged 18 to 65 years
2. Healthy as determined by the investigator on the basis of medical history, physical examination, clinical laboratory test results, vital signs, and 12-lead electrocardiogram
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bausch Health Americas, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Salix Pharmaceuticals

Principal Investigators

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Jeff Cohn

Role: STUDY_DIRECTOR

Bausch Health Americas, Inc.

Locations

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Lenexa, Kansas, United States

Site Status

Countries

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United States

Other Identifiers

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3200A3-102

Identifier Type: -

Identifier Source: org_study_id

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