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NCT02092571 · ClinicalTrials.gov registry record · Phase 1
A Pharmacokinetic Study to Evaluate the Bioequivalence of 2 Progesterone Vaginal Rings in Postmenopausal Women
A Phase 1 study, sponsored by Teva Branded Pharmaceutical Products R&D.
- Completed
- Registry status
- Phase 1
- Development phase
- 56
- Enrollment target
NCT02092571: Completed Phase 1 study, sponsored by Teva Branded Pharmaceutical Products R&D.
NCT02092571 is a Phase 1 study that has completed, run by Teva Branded Pharmaceutical Products R&D. The registered enrollment target is 56 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02092571, a Phase 1 study, has completed, sponsored by Teva Branded Pharmaceutical Products R&D.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 56 participants
- Enrollment target
Study Summary
A study to assess the pharmacokinetics of 2 progesterone vaginal rings in postmenopausal women
Interventions
- DRUG Progesterone vaginal ring,
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2014-02 |
| Est. Completion | 2014-08 |
| Phase | Phase 1 |
What the finished NCT02092571 record still lists
NCT02092571 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Progesterone vaginal ring, is the first listed.
NCT02092571 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02092571 about?
NCT02092571 is a clinical study titled "A Pharmacokinetic Study to Evaluate the Bioequivalence of 2 Progesterone Vaginal Rings in Postmenopausal Women". A study to assess the pharmacokinetics of 2 progesterone vaginal rings in postmenopausal women
What is the current status of trial NCT02092571?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 56 participants. The study started on 2014-02. Estimated completion is 2014-08.
What interventions are being tested in trial NCT02092571?
The interventions under investigation include: Progesterone vaginal ring, (DRUG).
Who is sponsoring clinical trial NCT02092571?
This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 167 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02092571's enrollment target sits among peer trials
56 902nd of 2000 higher than 1,083 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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