Ranibizumab in Combination With Proton Beam Irradiation for Choroidal Melanoma
Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
Details and patient eligibility
About
The purpose of the study is to investigate the safety and tolerability of the anti-VEGF (vascular endothelial cell growth factor) treatment, ranibizumab, in combination with proton beam irradiation for the treatment of choroidal melanoma by determining the incidence and severity of ocular adverse events. Systemic adverse events will also be evaluated. A secondary objective is to assess the efficacy of ranibizumab in reducing ocular complications that can occur after irradiation.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Patients with newly diagnosed choroidal melanoma undergoing proton therapy
- Tumors >15 mm in largest diameter and/or >5 mm in height
- Tumors ≤ 15 mm in largest diameter and ≤ 5 mm in height located ≤ 3 mm from optic disc and/or macula, with best-corrected visual acuity 20/100 or better in study eye
Exclusion criteria
- History of prior treatment for choroidal melanoma
- Pregnancy or lactation
- Presence of diabetic retinopathy
- History of retinal vascular occlusion or other retinal vascular disease
- Active ocular inflammation or history of uveitis in either eye
- History of uncontrolled glaucoma (defined as intraocular pressure >30mmHg despite treatment with anti-glaucoma medication) or filtering surgery in the study eye
- Previous intravitreal injections of Avastin® in the study eye or in the non-study eye within 30 days.
- Concurrent use of systemic anti-VEGF therapy
Trial design
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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