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NCT02159469 · ClinicalTrials.gov registry record · Phase 3
Subcutaneous Testosterone Replacement Efficacy and Safety in Adult Men Diagnosed With Hypogonadism
A Phase 3 study, sponsored by Antares Pharma.
- Completed
- Registry status
- Phase 3
- Development phase
- 150
- Enrollment target
NCT02159469: Completed Phase 3 study, sponsored by Antares Pharma.
NCT02159469 is a Phase 3 study that has completed, run by Antares Pharma. The registered enrollment target is 150 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02159469, a Phase 3 study, has completed, sponsored by Antares Pharma.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 150 participants
- Enrollment target
Study Summary
Evaluation of efficacy and safety of testosterone enanthate administered subcutaneously using an auto-injector
Primary Outcome
The primary objective of this study was to demonstrate the efficacy of QST (QuickShot Testosterone) administered subcutaneously once each week to adult males with hypogonadism.
Interventions
- COMBINATION_PRODUCT Testosterone enanthate auto-injector
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2014-07 |
| Est. Completion | 2015-11 |
| Phase | Phase 3 |
What the finished NCT02159469 record still lists
NCT02159469 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 1 intervention - of which Testosterone enanthate auto-injector is the first listed.
NCT02159469 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02159469 about?
NCT02159469 is a clinical study titled "Subcutaneous Testosterone Replacement Efficacy and Safety in Adult Men Diagnosed With Hypogonadism". Evaluation of efficacy and safety of testosterone enanthate administered subcutaneously using an auto-injector
What is the current status of trial NCT02159469?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 150 participants. The study started on 2014-07. Estimated completion is 2015-11.
What interventions are being tested in trial NCT02159469?
The interventions under investigation include: Testosterone enanthate auto-injector (COMBINATION_PRODUCT).
Who is sponsoring clinical trial NCT02159469?
This trial is sponsored by Antares Pharma, which has 9 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02159469's enrollment target sits among peer trials
150 1519th of 2000 higher than 455 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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