EYE001 to Treat Retinal Tumors in Patients With Von Hippel-Lindau Syndrome
Hippel-Lindau Disease
About this trial
This is an interventional treatment trial for Hippel-Lindau Disease focused on measuring Vision Loss, Optic Nerve Tumors, Macular Edema, Von Hippel-Lindau Disease, VEGF, EYE001, VHL
Eligibility Criteria
INCLUSION CRITERIA: Patient must understand and sign the informed consent. Patient must be at least 18 years of age. Patient must have retinal angiomas secondary to VHL in one or both eyes. Patient must have either optic nerve tumors or peripheral tumors that have caused central vision loss of 20/40 or worse. Patient must have clear ocular media and adequate papillary dilation to permit good quality stereoscopic fundus photography. Patients must be post menopausal, surgically sterile for at least 12 months prior to study entry, or agree to use at least two effective forms of birth control. All women of childbearing potential must have a negative serum pregnancy test at baseline and immediately prior to each injection and for at least 60 days following the last dose of EYE001. Patient must have lab values indicative of adequate hematological function (hemoglobin greater than or equal to 10 g/dl, platelet count less than or equal to 130 x 10(9)/I, WBC 3.8-10.8 x 10(9)/I) within one month of baseline. Patients must have lab values indicative of adequate liver function (serum bilirubin less than or equal to 1.5 mg/dl, SGOT/ALT, SGPT/AST, GGT and alkaline phosphotase within 2 x ULN) within one month of baseline. Patients must have lab values indicative of adequate renal function serum creatinine less than or equal to 2.0 mg/dl and BUN within 2.0 x ULN within one month of baseline. EXCLUSION CRITERIA: Significant media opacities, including cataract that precludes quality fundus photographs of the posterior pole. History or evidence of severe cardiac disease (electrocardiogram abnormalities, clinical history of unstable angina, acute coronary syndrome, myocardial infarction, revascularization procedure within 6 months prior to baseline, atrial or ventricular tachyarrythmias requiring ongoing treatment). History of stroke within 12 months of study entry. History of or current acute ocular or periocular infection (including any history of ocular herpes zoster). Any major surgical procedure within one month of study entry. Known serious allergies to fluorescein dye.
Sites / Locations
- National Eye Institute (NEI)