Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to evaluate the safety and clinical feasibility of the IRay System for the treatment of wet age-related macular degeneration (AMD).
The primary objective is to evaluate the safety and clinical feasibility of stereotactic radiotherapy with the Oraya IRay system for the treatment of choroidal neovascularization (CNV) associated with age-related macular degeneration (AMD), as measured by incidence and severity of ocular radiation related serious adverse events (SAE) and adverse events (AE) in subjects treated with an 11, 16 or 24 Gray (Gy) macular dose through the 60-month follow-up visit.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 11 Gy IRay | Experimental | Day 0 Lucentis followed by 11 Gy IRay, Lucentis at Month 1 and Lucentis PRN (N = 2) |
|
| 16 Gy IRay | Experimental | Day 0 Lucentis followed by 16 Gy IRay, Lucentis at Month 1 and Lucentis PRN (N = 27) |
|
| 16 Gy IRay - Radiation First | Experimental | 16 Gy IRay and Lucentis PRN (N = 13) |
|
| 24 Gy IRay | Experimental | Day 0 Lucentis followed by 24 Gy IRay, Lucentis at Month 1 and Lucentis PRN (N = 19) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| IRay | Device | Low voltage stereotactic radiotherapy system |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of ocular radiation-related adverse events | Month 12 |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of ocular adverse events | Through month 60 | |
| Percentage of subjects who lose at least 15 Early Treatment Diabetic Retinopathy Study (ETDRS) letters in best corrected visual acuity (BCVA) | Month 12 |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Denis O'Shaughnessy, Ph.D. | Oraya Therapeutics, Inc. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Asociación Para Evitar la Ceguera en México, I.A.P. | Mexico City | Delegación Coyoacán | 04030 | Mexico |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22895887 | Derived | Moshfeghi AA, Morales-Canton V, Quiroz-Mercado H, Velez-Montoya R, Zavala-Ayala A, Shusterman EM, Kaiser PK, Sanislo SR, Gertner M, Moshfeghi DM. 16 Gy low-voltage x-ray irradiation followed by as needed ranibizumab therapy for age-related macular degeneration: 12 month outcomes of a 'radiation-first' strategy. Br J Ophthalmol. 2012 Oct;96(10):1320-4. doi: 10.1136/bjophthalmol-2011-301222. Epub 2012 Aug 15. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Percentage of subjects gaining ≥ 15 ETDRS letters | Month 12 |
| Percentage of subjects gaining ≥ 0 ETDRS letters | Month 12 |
| Mean change in ETDRS visual acuity | Month 12 |
| Mean time to anti-VEGF retreatment following 2nd mandatory injection (excluding radiation-first subjects) | Month 12 |
| Mean total number of ranibizumab injections | Through month 12 and 24 |
| Change in choroidal neovascularization (CNV) size by fluorescein angiography (FA) | Month 12 |
| Change in total lesion size by fluorescein angiography (FA) | Month 12 |
| Change in central retinal lesion thickness by optical coherence tomography (OCT) | Month 12 |
| Change in central subfield thickness by optical coherence tomography (OCT) | Month 12 |
| ID | Term |
|---|---|
| D008268 | Macular Degeneration |
| D005128 | Eye Diseases |
| D012164 | Retinal Diseases |
| ID | Term |
|---|---|
| D012162 | Retinal Degeneration |
Not provided
Not provided