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NCT04285580 · ClinicalTrials.gov registry record · Phase 3
A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of Bimatoprost SR in Patients With Open-Angle Glaucoma or Ocular Hypertension
A Phase 3 study, sponsored by AbbVie.
- Completed
- Registry status
- Phase 3
- Development phase
- 37
- Enrollment target
NCT04285580: Completed Phase 3 study, sponsored by AbbVie.
NCT04285580 is a Phase 3 study that has completed, run by AbbVie. The registered enrollment target is 37 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04285580, a Phase 3 study, has completed, sponsored by AbbVie.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 37 participants
- Enrollment target
Study Summary
This study will evaluate the 24-hour intraocular pressure lowering effect and safety after a single administration of Bimatoprost SR in patients with Open-Angle Glaucoma or Ocular Hypertension
Primary Outcome
IOP is a measurement of the fluid pressure inside the study eye. A negative change from baseline indicates an improvement and a positive change from baseline indicates a worsening.
Interventions
- DRUG Bimatoprost SR
- DRUG LUMIGAN
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2020-06-11 |
| Est. Completion | 2022-05-14 |
| Phase | Phase 3 |
What the finished NCT04285580 record still lists
NCT04285580 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which Bimatoprost SR is the first listed.
NCT04285580 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04285580 about?
NCT04285580 is a clinical study titled "A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of Bimatoprost SR in Patients With Open-Angle Glaucoma or Ocular Hypertension". This study will evaluate the 24-hour intraocular pressure lowering effect and safety after a single administration of Bimatoprost SR in patients with Open-Angle Glaucoma or Ocular Hypertension
What is the current status of trial NCT04285580?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 37 participants. The study started on 2020-06-11. Estimated completion is 2022-05-14.
What interventions are being tested in trial NCT04285580?
The interventions under investigation include: Bimatoprost SR (DRUG), LUMIGAN (DRUG).
Who is sponsoring clinical trial NCT04285580?
This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04285580's enrollment target sits among peer trials
37 1901st of 2000 higher than 100 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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