Under construction – not a live service
Sign in
Taking people in United StatesPhase 3

Tests an eye implant with a new lens against eye drops in cataract patients

Tests a bimatoprost eye implant with a lens against timolol drops in glaucoma patients.

Plain-language title generated from the registry record
Registry title: Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compared to Timolol Ophthalmic Solution (Rhine)

Key facts

Where
Houston, United StatesSee the site
Phase
Phase 3

Where in United States

  • Houston Eye AssociatesHouston, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
SpyGlass Pharma, Inc.
Trial code
NCT07218783
Record updated
20 October 2025
Original description
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.Read full original descriptionShow less

A Prospective, Multicenter, Randomized, Masked, Controlled Study to Evaluate the Safety and Efficacy of the Bimatoprost Implant System (78 mcg) Used in Combination With the SpyGlass IOL Compared to Timolol Maleate Ophthalmic Solution, USP, 0.5%,

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.

Inclusion: Diagnosis of mild to moderate open-angle glaucoma or ocular hypertension; Planned removal of cataract; Female participants of childbearing potential must have a negative urine pregnancy test at the baseline visit and agree to the use of contraception.

Exclusion: Uncontrolled systemic disease; History of incisional/refractive corneal surgery; History of incisional glaucoma surgery or intraocular injections; Other ocular diseases, pathology, or conditions; Any glaucoma diagnosis other than OHT, open-angle, pseudoexfoliative, or pigmentary glaucoma.

ClinicalTrials.gov NCT07218783