Study Evaluating the Safety and Tolerability of SCA-136 in Healthy Japanese Male Subjects

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

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-07-31

Study Completion Date

2007-10-31

Brief Summary

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This study is being conducted to assess the safety and tolerability of ascending multiple oral doses of SCA-136 administered to healthy Japanese male subjects.

Detailed Description

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Conditions

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Schizophrenia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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SCA-136

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healty Japanese men willing to use a medically acceptable form of contraception.

Exclusion Criteria

* Any significant disease
* Positive urine drug screen
* Increased liver function tests
* Use of prescription drugs.

Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Principal Investigators

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Medical Monitor

Role: STUDY_DIRECTOR

Wyeth is now a wholly owned subsidiary of Pfizer

Locations

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Ikebukuro, Toshima-ku, Japan

Site Status

Countries

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Japan

Other Identifiers

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3153A1-1114

Identifier Type: -

Identifier Source: org_study_id