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Spots Global Cancer Trial Database for Study to Evaluate the Safety and Efficacy of Androxal Treatment in Men With Secondary Hypogonadism

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Trial Identification

Brief Title: Study to Evaluate the Safety and Efficacy of Androxal Treatment in Men With Secondary Hypogonadism

Official Title: An Open-Label, Multiple Center Study to Evaluate the Safety and Efficacy of Androxal™ Treatment in Men With Secondary Hypogonadism Who Completed ZA-003

Study ID: NCT01067365

Interventions

Androxal
Androxal

Study Description

Brief Summary: Subjects who completed ZA-003 were eligible to receive an additional year of treatment in this extension study.

Detailed Description: The objectives of this study were to evaluate the safety and efficacy of Androxal® administered orally once daily for one year in men with secondary hypogonadism and who had completed ZA-003.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Alabama Clinical Therapeutics, LLC, Birmingham,, Alabama, United States

Medial Affiliated Research Center, Inc., Huntsville, Alabama, United States

Northern California Research Corp, Carmichael, California, United States

Prime-Care Clinical Research, Mission Viejo, California, United States

Harbor-UCLA Medical Center, Torrance, California, United States

Chase Medical Research, LLC, Waterbury, Connecticut, United States

Southeastern Research Group, Inc., Tallahassee,, Florida, United States

Northeast Indiana Research, LLC, Fort Wayne, Indiana, United States

Commonweatlh Biomedical Research, Madisonville,, Kentucky, United States

The Center for Sexual Medicine at Sheppard Pratt, Baltimore, Maryland, United States

Office of Keith Pierce, MD, Livonia, Michigan, United States

Office of Michael Mall, MD, Las Vegas, Nevada, United States

Office of Stephen Miller, MD, Las Vegas, Nevada, United States

Advanced Biomedical Research, Inc., Hackensack, New Jersey, United States

Office of Gary S. Karlin, MD, Lawrenceville, New Jersey, United States

Medical Research Associates of Nashville, Nashville, Tennessee, United States

Urology San Antonio Research, PA, San Antonio, Texas, United States

Salt Lake Research, Salt Lake City, Utah, United States

Contact Details

Name: Andre van As, MD, PhD

Affiliation: Repros Therapeutics Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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