Study Evaluating 3 New Formulations of SKI-606 in Healthy Adult 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

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-07-31

Study Completion Date

2007-09-30

Brief Summary

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To evaluate the comparative bioavailability of 3 new tablet formulations of SKI-606 with a reference capsule and an oral solution in healthy subjects.

Detailed Description

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Conditions

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Healthy

Keywords

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healthy subjects

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Blinding Strategy

NONE

Interventions

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SKI-606

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Criteria:

* Healthy male and female aged 18 to 50 years.
* Women of nonchildbearing potential (WONCBP).

Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

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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San Antonio, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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3160A4-1109

Identifier Type: -

Identifier Source: org_study_id