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Clinical Trials/NCT00505973
NCT00505973
Completed
Phase 1

An Ascending Multiple Dose Study of the Safety, Pharmacokinetics, and Pharmacodynamics of SCA-136 Administered Orally to Healthy Japanese Male Subjects

Wyeth is now a wholly owned subsidiary of Pfizer0 sites24 target enrollmentJuly 2007
ConditionsSchizophrenia
DrugsSCA-136

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Enrollment
24
Primary Endpoint
Adverse events, safety laboratory results, vital signs, and ECGs will be used to monitor subject safety.
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
July 2007
End Date
October 2007
Last Updated
18 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adverse events, safety laboratory results, vital signs, and ECGs will be used to monitor subject safety.

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