Wills Eye
Trial Pipeline
Caffeine Consumption in Glaucoma Patients and Healthy Subjects
NCT03675412
Novel Glaucoma Diagnostics
NCT00286637
A Multi-Center Study on the Use of Rho-Kinase Inhibitor to Reduce or Prevent PVR in RRD Eyes at High Risk for PVR
NCT05660447
Evaluating Home Testing Devices for the Management of Glaucoma
NCT05325996
Handheld Vibrator Versus Topical Eye Drops as Anesthesia for Intravitreal Injections
NCT03079713
30g vs 33g Needle for Intravitreal Injections
NCT03038048
Eplerenone for the Treatment of Central Serous Chorioretinopathy
NCT01990677
Comparing the Effect of the Water Drinking Test on Intraocular Pressure
NCT02001155
The Safety & Efficacy of Intravitreal Aflibercept Injection in Patients With Persistent Central Serous Chorioretinopathy
NCT01710332
How Similar Are Changes to the Surface of the Eye When Two Different Glaucoma Eye Drops Are Used?
NCT00798694
Will Listening to Music Make it Easier to Take a Visual Field Test?
NCT01027039
Lucentis Versus Mitomycin C During Glaucoma Surgery
NCT00626782
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 3 |
| Phase 4 | 1 |
Therapeutic Areas
What the Pipeline for Wills Eye Shows
According to the ClinicalTrials.gov registry, Wills Eye is linked to 12 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting — about 17% of the sponsor's indexed portfolio — and 9 are already marked complete, representing roughly 75% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for Wills Eye reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 3 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for Wills Eye is Glaucoma with 5 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.