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NCT06120842 · ClinicalTrials.gov registry record · Phase 1

Evaluation of the Bimatoprost Implant System Used in Combination With the SpyGlass Intraocular Lens Compared to Timolol Ophthalmic Solution

A Phase 1 study of Glaucoma and Cataract, sponsored by SpyGlass Pharma.

Active
Registry status
Phase 1
Development phase
201
Enrollment target
1
Study location

NCT06120842: Active Phase 1 study of Glaucoma and Cataract, sponsored by SpyGlass Pharma.

NCT06120842 is a Phase 1 study of Glaucoma and Cataract that is active but no longer recruiting, run by SpyGlass Pharma. The registered enrollment target is 201 participants, below the 908-participant average among 92 other Glaucoma trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06120842, a Phase 1 study of Glaucoma and Cataract, is active but no longer recruiting, sponsored by SpyGlass Pharma.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
201 participants
Enrollment target
1
Study location

Study Summary

This trial is a randomized study to evaluate and compare two doses of 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.

Primary Outcome

Time matched mean IOP reduction from Baseline (mmHg) in the study eyes at all the individual IOP timepoints

Interventions

  • DEVICE SpyGlass IOL
  • DRUG Timolol Maleate Ophthalmic Solution, 0.5%
  • DRUG Bimatoprost Implant System (High Dose)
  • DRUG Bimatoprost Implant System (Low Dose)
  • DEVICE Commercially Available Aspheric Monofocal Non-Yellow Chromophore IOL

Study Locations (1)

Arizona

  • Arizona Advanced Eye Research Institute - Glendale

Trial Details

FieldValue
Enrollment Target 201 participants
Start Date 2023-10-13
Est. Completion 2027-11
Phase Phase 1
SpyGlass Pharma

3 total trials

What the registry record for NCT06120842 still lists

NCT06120842 is an interventional study that assigns participants to a tested intervention. The registered 201 participants enrollment target is mid-sized for trials with a published cap, below the 908-participant average among 92 other Glaucoma trials with a reported enrollment target (78% lower).

The record links to 3 conditions, with Glaucoma appearing as the primary indexed condition, and to 5 interventions - of which SpyGlass IOL is the first listed.

NCT06120842 reports a single indexed study location in Arizona.

Frequently Asked Questions

What is clinical trial NCT06120842 about?

NCT06120842 is a clinical study titled "Evaluation of the Bimatoprost Implant System Used in Combination With the SpyGlass Intraocular Lens Compared to Timolol Ophthalmic Solution". This trial is a randomized study to evaluate and compare two doses of 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.

What is the current status of trial NCT06120842?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 201 participants. The study started on 2023-10-13. Estimated completion is 2027-11.

What conditions does trial NCT06120842 study?

This clinical trial studies the following conditions: Glaucoma, Cataract, Ocular Hypertension.

What interventions are being tested in trial NCT06120842?

The interventions under investigation include: SpyGlass IOL (DEVICE), Timolol Maleate Ophthalmic Solution, 0.5% (DRUG), Bimatoprost Implant System (High Dose) (DRUG), Bimatoprost Implant System (Low Dose) (DRUG), Commercially Available Aspheric Monofocal Non-Yellow Chromophore IOL (DEVICE).

Who is sponsoring clinical trial NCT06120842?

This trial is sponsored by SpyGlass Pharma, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06120842 being conducted?

This trial has 1 study location across Arizona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Glaucoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06120842's enrollment target sits among peer trials

201 26th of 92 higher than 67 of 92 other Glaucoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Glaucoma 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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Source: ClinicalTrials.gov NCT06120842, the US trial registry maintained by the National Library of Medicine. NCT06120842 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.