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Completed Phase 3 Interventional Results available

Subcutaneous Testosterone Replacement Efficacy and Safety in Adult Men Diagnosed With Hypogonadism

ClinicalTrials.gov ID: NCT02159469

Public ClinicalTrials.gov record NCT02159469. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 6:44 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multiple-dose, 52-week Study to Evaluate the Efficacy and Safety of Testosterone Enanthate Administered Subcutaneously Once Each Week to Adult Males With Hypogonadism

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Evaluation of efficacy and safety of testosterone enanthate administered subcutaneously using an auto-injector

Study identification

NCT ID
NCT02159469
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Antares Pharma Inc.
Industry
Enrollment
150 participants

Conditions and interventions

Conditions

Interventions

Combination Product

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2014 (Type not available)
Primary completion
Feb 2015 (Actual)
Completion
Nov 2015 (Actual)
Last update posted
Feb 7, 2018

2014 – 2015

United States locations

U.S. sites
28
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Huntsville Alabama — —
Not listed Tucson Arizona — —
Not listed Burbank California — —
Not listed Torrance California — —
Not listed Upland California — —
Not listed Jacksonville Florida — —
Not listed Oviedo Florida — —
Not listed Lexington Kentucky — —
Not listed Shreveport Louisiana — —
Not listed Brookline Massachusetts — —
Not listed Methuen Massachusetts — —
Not listed Kansas City Missouri — —
Not listed Lawrenceville New Jersey — —
Not listed Albany New York — —
Not listed New York New York — —
Not listed Rochester New York — —
Not listed Franklin Ohio — —
Not listed Medford Oregon — —
Not listed Warwick Rhode Island — —
Not listed Mt. Pleasant South Carolina — —
Not listed Nashville Tennessee — —
Not listed San Antonio Texas — —
Not listed Sugar Land Texas — —
Not listed West Valley City Utah — —
Not listed Norfolk Virginia — —
Not listed Richmond Virginia — —
Not listed Renton Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02159469, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 7, 2018 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02159469 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →