Evaluation of the Bimatoprost Implant System Used in Combination With the SpyGlass Intraocular Lens Compared to Timolol Ophthalmic Solution
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Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
201actual
Sites
1
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2023-10-13 | actual | When the study began enrolling |
| Primary completion | 2025-01-31 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Nov 2027 | estimated | The whole study's end, after follow-up |
| First posted | 2023-11-07 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-08-22 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Cataract
- Glaucoma
- Ocular Hypertension
Interventions
- Drug: Bimatoprost Implant System (High Dose)
- Drug: Bimatoprost Implant System (Low Dose)
- Drug: Timolol Maleate Ophthalmic Solution, 0.5%
- Device: Commercially Available Aspheric Monofocal Non-Yellow Chromophore IOL
- Device: SpyGlass IOL
Primary outcome
what the primary-completion date above is the date OFMean IOP Reduction from Baseline (mmHg)
measured Weeks 2 and 6, and Month 3
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