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COMPLETED Phase 3

Safety and Efficacy Trial of Testosterone Undecanoate

NCT01765179 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to determine if oral testosterone undecanoate is effective and safe in the treatment of low testosterone in men.

Conditions Studied

Interventions

  • DRUG Oral testosterone undecanoate

Study Locations (20)

California

  • SC Clinical Research, Inc. — Garden Grove
  • South ORange County Endocrinology — Laguna Hill
  • Tower Urology, Tower Research Institute — Los Angeles
  • San Diego Sexual Medicine — San Diego
  • LABiomedical Research Institute at Harbor-UCLA Medical Center — Torrance

Arizona

  • Precision Trials/Valley Urologic Associates — Glendale
  • Premier Clinical Research Center — Phoenix
  • Precision Trials/Valley Urologic Associates — Phoenix
  • Quality of LIfe Medical and Research Center — Tucson

Florida

  • South Florida Medical Research — Aventura
  • PAB Clinical Research — Brandon
  • Innovative Research of West Florida — Clearwater
  • Jacksonville Impotence Treatment Center — Jacksonville

Alabama

  • Alabama Clinical Therapeutics, LLC — Birmingham
  • Alabama Internal Medicine, PC — Birmingham
  • Medical Affliated Research Center, Inc. — Huntsville

Connecticut

  • Conneticut Clinical Research Center — Middlebury

New York

  • University Urology Associates — New York

Oregon

  • Sunstone Medical Research — Medford

Pennsylvania

  • Unrologic Consultants of SE Pennsylvania — Bala-Cynwyd

Trial Details

FieldValue
Enrollment Target 144 participants
Start Date 2013-01
Est. Completion 2013-07
Phase Phase 3

Sponsor

Clarus Therapeutics

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01765179

The ClinicalTrials.gov registry entry for NCT01765179 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 144 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clarus Therapeutics, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Male Hypogonadism appearing as the primary indexed condition, and to 1 intervention — of which Oral testosterone undecanoate is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01765179 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Arizona, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01765179 about?

NCT01765179 is a clinical study titled "Safety and Efficacy Trial of Testosterone Undecanoate". The purpose of the study is to determine if oral testosterone undecanoate is effective and safe in the treatment of low testosterone in men.

What is the current status of trial NCT01765179?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 144 participants. The study started on 2013-01. Estimated completion is 2013-07.

What conditions does trial NCT01765179 study?

This clinical trial studies the following conditions: Male Hypogonadism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01765179?

The interventions under investigation include: Oral testosterone undecanoate (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01765179?

This trial is sponsored by Clarus Therapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01765179 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial