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NCT07154810
Observational Study to Evaluate Long Term Outcomes for Ocular Hypertension and Glaucoma Patients Treated With the SpyGlass Bimatoprost Implant System / IOL Combination
trial in Glaucoma in 23 participants. Participants enrolled and being followed up; not accepting new ones.
14 April 2031
Quick facts
| Lead sponsor | SpyGlass Pharma, Inc. |
|---|---|
| Status | Active, enrolled |
| Study type | OBSERVATIONAL |
| Enrollment | 23 |
| Start date | 16 March 2023 |
| Primary completion | 14 April 2031 |
| Estimated completion | 14 April 2031 |
| Sites | 1 location across Honduras |
Conditions studied
- Glaucoma — all drugs for Glaucoma →
- Cataract — all drugs for Cataract →
- Ocular Hypertension — all drugs for Ocular Hypertension →
Sponsor
SpyGlass Pharma, Inc. — full company profile →
Who can join
Eligibility, any sex, with Glaucoma or Cataract. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to further observe and learn if the SpyGlass Pharma Bimatoprost Implant System / IOL Combination works to treat cataracts and either ocular hypertension or glaucoma. It will also further observe and learn about the safety of the Bimatoprost Implant System / IOL Combination. The main questions it aims to answer are: * Does the Bimatoprost Implant System / IOL Combination continue lower the pressure inside the eye to treat ocular hypertension or glaucoma long term? * Does the Bimatoprost Implant System / IOL Combination continue to correct vision after cataract surgery long term? * What long term medical problems do participants have when treated with the Bimatoprost Implant System / IOL Combination?
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Prospective Pilot Study of Sustained Release Bimatoprost Implant with SpyGlass Intraocular Lens: 3-Year Results.
Tan NE, Katz G, Robles M, Gupta PK, et al · · 2026 · PMID 41621045 · DOI 10.1007/s40123-026-01313-4
Verify or expand the search:
- PubMed search for NCT07154810
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other SpyGlass Pharma, Inc. trials
Trials by the same sponsor.
- NCT07218796 — Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compar · Phase 3 · recruiting
- NCT07218783 — Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compar · Phase 3 · recruiting
- NCT07154797 — Evaluation of the Safety and Effectiveness of the Bimatoprost Implant System / IOL Combination in Patients With Ocular H · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07154810 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by SpyGlass Pharma, Inc.
- Last refreshed: 4 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07154810.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing