An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men



Status:Completed
Conditions:Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 80
Updated:5/5/2014
Start Date:March 2014
End Date:June 2015
Contact:Leasia Hill
Email:leasia.hill@abbvie.com
Phone:847-938-0907

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A Multicenter, Open-Label, Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men

This is an open-study with a 26 week open label treatment period followed by an optional 26
week open label extension. The total treatment period will be 52 weeks.


Inclusion Criteria:

Low testosterone

Exclusion Criteria:

- Normal testosterone levels

- Elevated Prostatic Specific Antigen (PSA)

- History of breast or prostate cancer
We found this trial at
41
sites
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Albuquerque, NM
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Anaheim, CA
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Austin, TX
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Bala Cynwyd, Pennsylvania 19004
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Bala Cynwyd, PA
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Birmingham, AL
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Charlotte, North Carolina 28207
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Charlotte, NC
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Chattanooga, TN
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Clearwater, FL
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Cleveland, OH
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Colorado Springs, Colorado 80910
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Colorado Springs, CO
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Crestview Hills, Kentucky 41017
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Crestview Hills, KY
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Dallas, TX
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Denver, CO
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Dunwoody, GA
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Garden City, NY
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Greer, SC
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Huntsville, AL
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Jacksonville, FL
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Jenkintown, PA
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Las Vegas, NV
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Las Vegas, NV
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LawrenceVille, New Jersey 08648
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LawrenceVille, NJ
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Lexington, KY
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Los Angeles, CA
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Los Gatos, CA
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Mesa, AZ
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Methuen, MA
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Middlebury, CT
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Morehead City, North Carolina 28557
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Morehead City, NC
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Phoenix, AZ
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Ponte Vedra Beach, Florida 32081
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Poughkeepsie, NY
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Salisbury, North Carolina 28144
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Salisbury, NC
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San Antonio, TX
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Wichita, KS
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