Melanoma Clinical Trial

Intravitreal Faricimab Injections or Fluocinolone Acetonide (0.19 mg) Intravitreal Implants vs Observation for Prevention of VA Loss Due to Radiation Retinopathy

Summary

This randomized controlled trial will evaluate the effect of intravitreal faricimab or fluocinolone acetonide (FAc) intravitreal implant compared with observation on long-term visual acuity following treatment of choroidal melanoma with iodine-125 plaque brachytherapy.

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Full Description

The primary objectives are to compare long-term visual acuity outcomes in eyes that receive repeated treatment with faricimab or fluocinolone acetonide intravitreal implants with those observed initially and treated only if macular edema (ME) develops. The secondary objectives are to determine if repeated treatment with faricimab or fluocinolone acetonide intravitreal implants versus observation can prevent or alter the course of ME from radiation retinopathy and to evaluate the natural history of radiation retinopathy with multimodal imaging including widefield color photographs, widefield fluorescein angiography and OCTA.

View Eligibility Criteria

Eligibility Criteria

Key Inclusion Criteria

Primary uveal melanoma (excluding iris melanoma) receiving primary treatment with plaque brachytherapy
Absence of unrelated cause of visual loss
Baseline visual acuity ≥ 34 letters (20/200 Snellen equivalent or better)
Posterior tumor margin >0 mm from the center of the macula (i.e., tumor is NOT under the geometric center of the fovea)
Posterior tumor margin >0 mm from the closest disc margin (i.e., tumor is not touching the edge of the optic disc)
Calculated total dose to center of the macula ≥30 Gy

Key Exclusion Criteria

Opaque media
Inability to undergo fluorescein angiography
Less than 18 years of age
Prior vitrectomy
Intraocular pressure (IOP) ≥ 25 mmHg or history of steroid- induced IOP elevation that required treatment at baseline
IOP ≥ 25 mmHg at randomization or increase in IOP ≥ 8 mmHg from baseline to randomization (following steroid challenge

Study is for people with:

Melanoma

Phase:

Phase 3

Estimated Enrollment:

600

Study ID:

NCT05844982

Recruitment Status:

Recruiting

Sponsor:

Jaeb Center for Health Research

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There are 10 Locations for this study

See Locations Near You

Retina Associates of Florida, LLC
Tampa Florida, 33609, United States More Info
Ivan J. Suner, MD
Contact
813-875-6373
[email protected]
Midwest Eye Institute
Indianapolis Indiana, 46290, United States More Info
John Minturn
Contact
317-817-1414
[email protected]
University of Iowa Department of Ophthalmology and Visual Sciences
Iowa City Iowa, 52242, United States More Info
Elaine M. Binkley, MD
Contact
319-356-3185
[email protected]
Mayo Clinic
Rochester Minnesota, 55905, United States More Info
Lauren Dalvin, MD
Contact
507-538-8119
[email protected]
Retina Research Institute, LLC
Saint Louis Missouri, 63128, United States More Info
Bradley T. Smith, MD
Contact
314-367-1181
[email protected]
The Cleveland Clinic Foundation DBA Cleveland Clinic Lerner College of Medicine
Cleveland Ohio, 44120, United States More Info
Arun D. Singh, MD
Contact
216-445-9519
[email protected]
Retina-Vitreous Consultants, Inc.
Monroeville Pennsylvania, 15146, United States More Info
Robert L. Bergren, MD
Contact
412-683-5300
[email protected]
Retina Consultants of Carolina, PA
Greenville South Carolina, 29605, United States More Info
Chris S. Bergstrom, MD
Contact
864-233-5722
[email protected]
Tennessee Retina, PC
Nashville Tennessee, 37203, United States More Info
David A. Reichstein, MD
Contact
615-983-6000
[email protected]
Texas Retina Associates
Lubbock Texas, 79424, United States More Info
Michel Shami, MD
Contact
806-792-0066
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 3

Estimated Enrollment:

600

Study ID:

NCT05844982

Recruitment Status:

Recruiting

Sponsor:


Jaeb Center for Health Research

How clear is this clinincal trial information?

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