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NCT05393895 · ClinicalTrials.gov registry record · Phase 3
An Evaluation of the Safety of CSF-1 in Presbyopic Subjects
A Phase 3 study, sponsored by Orasis Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 178
- Enrollment target
NCT05393895: Completed Phase 3 study, sponsored by Orasis Pharmaceuticals.
NCT05393895 is a Phase 3 study that has completed, run by Orasis Pharmaceuticals. The registered enrollment target is 178 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05393895, a Phase 3 study, has completed, sponsored by Orasis Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 178 participants
- Enrollment target
Study Summary
This is a multi-center, double-masked, vehicle-controlled study. The purpose of the study is to evaluate the safety of CSF-1 compared with vehicle in presbyopic subjects. Subjects will be treated for at least 6 weeks.
Primary Outcome
As this is a safety study, no efficacy outcome has been defined.
Interventions
- DRUG Vehicle
- DRUG CSF-1
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 178 participants |
| Start Date | 2022-04-22 |
| Est. Completion | 2022-12-01 |
| Phase | Phase 3 |
What the finished NCT05393895 record still lists
NCT05393895 is an interventional study that assigns participants to a tested intervention. The registered 178 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 (77% lower).
The record links to 0 conditions, and to 2 interventions - of which Vehicle is the first listed.
NCT05393895 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05393895 about?
NCT05393895 is a clinical study titled "An Evaluation of the Safety of CSF-1 in Presbyopic Subjects". This is a multi-center, double-masked, vehicle-controlled study. The purpose of the study is to evaluate the safety of CSF-1 compared with vehicle in presbyopic subjects. Subjects will be treated for at least 6 weeks.
What is the current status of trial NCT05393895?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 178 participants. The study started on 2022-04-22. Estimated completion is 2022-12-01.
What interventions are being tested in trial NCT05393895?
The interventions under investigation include: Vehicle (DRUG), CSF-1 (DRUG).
Who is sponsoring clinical trial NCT05393895?
This trial is sponsored by Orasis Pharmaceuticals, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05393895's enrollment target sits among peer trials
178 1437th of 2000 higher than 563 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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