Testosterone MD-Lotion Residual Washing Study

NCT ID: NCT00996151

Last Updated: 2010-03-02

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

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-12-31

Study Completion Date

2010-02-28

Brief Summary

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The study will evaluate the amount of Testosteron MD-Lotion 2% remaining on the axilla after a single dose application in healthy males who undergo a post dose washing procedure.

Detailed Description

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Conditions

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Hypergonadism

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Interventions

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Testosterone MD-Lotion

Single dose Testosterone MD-Lotion 2%

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healthy male subjects ≥18 and ≤ 70 years

Exclusion Criteria

* Disqualifying concurrent condition or allergy/sensitivity to Testosterone MD-Lotion
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Acrux DDS Pty Ltd

INDUSTRY

Sponsor Role lead

Responsible Party

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Acrux Pharma Pty Ltd

Principal Investigators

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Tina Soulis, PhD

Role: STUDY_DIRECTOR

Acrux Pharma Pty Ltd

Locations

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QPharm Pty Ltd

Brisbane, Queensland, Australia

Site Status

Countries

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Australia

Other Identifiers

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MTE11

Identifier Type: -

Identifier Source: org_study_id

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