← Eichor
Study identifier: NCT07218783 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compared to Timolol Ophthalmic Solution (Rhine)

Condition: Cataract · Glaucoma · Ocular Hypertension  ·  Sponsor: SpyGlass Pharma, Inc.

PhasePhase 3
Planned participants400
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

This trial is a randomized study to evaluate the Bimatoprost Implant System used in combination with the SpyGlass IOL to Timolol Ophthalmic Solution in participants with mild to moderate open-angle glaucoma or ocular hypertension undergoing cataract surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Director, Clinical Affairs  ·  949-284-6904  ·  clinical@spyglasspharma.com

Always discuss trial participation with your own doctor first.

Locations (1)

Houston Eye AssociatesHouston, Texas, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07218783