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Clinical Trials/NCT00434187
NCT00434187CompletedPhase 1

An Ascending Multiple Dose Study of the Safety, Tolerability and Pharmacokinetics of ERB-041 Administered Orally to Healthy, Female Japanese Subjects

Wyeth is now a wholly owned subsidiary of Pfizer1 site in 1 country24 target enrollmentStarted: August 1, 2006Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Completed
Sponsor
Enrollment
24
Locations
1
Primary Endpoint
safety, pharmacokinetics

Study Overview

Brief Summary

The primary objective is evaluate the safety, tolerability, and pharmacokinetics of multiple doses of ERB-041, an investigational drug, in healthy, female Japanese subjects.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
Double

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Healthy as determined by the investigator on the basis of medical history and screening evaluations.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

safety, pharmacokinetics

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Sponsor Class
Industry

Study Sites (1)

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