Study Evaluating SKI-606 Administered to Healthy 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

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Study Completion Date

2007-08-31

Brief Summary

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Safety and tolerability of SKI-606 in healthy subjects; the influence of food intake on the same.

Detailed Description

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Conditions

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Healthy

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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SKI-606

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healthy

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

Trial Manager

Role: PRINCIPAL_INVESTIGATOR

For Netherlands, [email protected]

Locations

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Utrecht, , Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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3160A1-103

Identifier Type: -

Identifier Source: org_study_id