Carbidopa-Levodopa in Dry AMD With Geographic Atrophy

Summary

Participation Requirements

Description

Age-related macular degeneration (AMD) is the most common cause of blindness, in individuals over the age of 50, in the developed world. AMD becomes more common as people age, and is more common in lightly pigmented individuals. AMD appears more common in patients with Parkinson's Disease, than in t...

Age-related macular degeneration (AMD) is the most common cause of blindness, in individuals over the age of 50, in the developed world. AMD becomes more common as people age, and is more common in lightly pigmented individuals. AMD appears more common in patients with Parkinson's Disease, than in those without. The AREDS nutritional supplements are effective in slowing the progress of intermediate AMD(5). Most AMD is "dry AMD", which progresses relatively slowly and may impair vision, but usually does not lead to legal blindness. There are two forms of AMD, "wet AMD" and geographic atrophy (GA), that can cause more profound vision loss. In aggregate they occur in about 25% patients with AMD. Wet AMD is due to new growth of abnormal blood vessels under the retina. The new blood vessels are believed to be due to an excessive release of vascular endothelial growth factor (VEGF) by the retinal pigment epithelium(RPE) cells. Wet AMD is now effectively treated with intraocular injections of VEGF inhibitors. Geographic Atrophy, the other form of advanced AMD, represents focal death of the RPE cells and overlying neurosensory retina. There is no current treatment for GA. It is suspected that GA is due in part to a localized inflammatory response, damage to RPE cells and loss of RPE cell function. It may also be speculated that stimulation of RPE cells to release a potent neurotrophic factor, pigment epithelium derived factor (PEDF) may slow progression of GA. In 2008, Dr. Brian McKay identified a receptor, G protein coupled receptor #143(GPR143), on the surface of RPE cells and discovered that L-DOPA was the natural ligand or stimulator of GPR143. Dr McKay showed that treatment of RPE cells with exogenous L-DOPA resulted in the release of additional PEDF. In subsequent work Dr McKay's group also showed that L-DOPA stimulation of PEDF in RPE cells was also associated with a decrease in VEGF. Thus, Dr McKay hypothesized that exogenous LDOPA may prevent the onset of AMD or progression to wet AMD. In 2015, Dr McKay and his associates published a paper that showed that patients, who had been treated with L-DOPA, had a delay in the onset of AMD by 8 years, compared to patients who had not been treated with L-DOPA. In addition, those who had AMD and went on to develop wet AMD, did so 5 years later than those with no history of L-DOPA treatment. L-DOPA is an intermediate in the pigmentation pathway. Dr McKay and his associates suggested that the reason darkly pigmented races do not get AMD nearly as frequently as lighter pigmented races, is that they produce more pigment, and thus more L-DOPA to stimulate GPR143 on RPE cells. According to this hypothesis, the stimulated RPE cells release PEDF and decrease VEGF, which together are responsible for the protective effect. Pharmacology of L-DOPA and carbidopa: L-DOPA is formed by 3-hydroxylation of tyrosine by tyrosine-3-monooxygenase (tyrosinase).(18) The primary metabolic pathway of L-DOPA is decarboxylation by amino acid decarboxylase to dopamine, which is responsible for most, but not all, of its pharmacologic effects and toxicity. When carbidopa is administered with LDOPA, systemic levels of L-DOPA double and central nervous system (CNS) L-DOPA increases from about 1% of the administered dose to about 4%. Levodopa freely passes from the systemic circulation into the retina and brain, but dopamine and carbidopa do not. Adverse events are markedly decreased when carbidopa is administered with L-DOPA, because systemic levels of the toxic metabolite of L-DOPA, dopamine, are markedly reduced. In most patients, 25 mg of carbidopa is sufficient to control side effects of 100 mg of L-DOPA, primarily nausea, by 90%. L-DOPA is the natural ligand for GPR143 in the RPE cells. The Investigators' intent is to increase the L-DOPA available to RPE surface receptors (GPR 143) while minimizing peripheral toxicity. This concept is unique, because all other uses of L-DOPA rely on CNS conversion of L-DOPA to dopamine, in order to produce the desired effect. Since there are no established animal models for AMD, and L-DOPA has a good safety profile in healthy volunteers and patients with Parkinson's disease, the Investigators propose a prospective experiment to determine the safety and tolerability of L-DOPA, in a population of patients with AMD. The participants will be made aware of potential side effects of L-DOPA, which are listed in the Informed Consent, during the consent process. Adverse events will be elicited by questioning the participants at each visit. The participants will also be advised to call the site, if they have any medical problem between visits. The Investigators will also use this study to examine whether L-DOPA has a positive effect on visual acuity and pathologic retinal changes of "dry" AMD with geographic atrophy. The parameters to be evaluated are best corrected ETDRS visual acuity, area of geographic atrophy by Fundus AutoFluorescence (FAF), macular thickness by spectral domain optical coherence tomography (SD OCT), new blood (hemorrhage) by direct retinal examination, and subjective decrease in vision. Treatments: Study participants will receive randomly assigned, single blind, commercially available carbidopa-levodopa 25-100 mg, two tablets once daily hs, or two tablets dosed TID (three times daily), in the morning, with supper and hs for one month, or placebo two tablets dosed three times daily, in the morning, with supper and hs (200-600 mg of levodopa daily). This is the equivalent of low to moderate doses of carbidopa-levodopa in patients with Parkinson's disease (daily dose of levodopa 200-800 mg). If a study participant experiences non-serious, but bothersome adverse effects while taking the study medication, the dose may be reduced to 1 tablet hs, or 1 tablet TID. Number of subjects: 154 randomized. Duration: 12 months of treatment, with visits at Baseline, 1 week, 1 month, 3 months, 6 months, 9 months and 12 months. Primary Endpoint: A statistically significant difference in progression of area of geographic atrophy with carbidopa-levodopa treatment compared to treatment with placebo. Measurements and Activities: Informed Consent at Baseline; Ophthalmic history and comprehensive eye examination; including visual acuity, with best optical correction, using an EDTRS chart, in both eyes prior to randomization, ophthalmoscopic examination, a subjective vision questionnaire and SD OCT with FAF; Repeat assessment of visual acuity using an EDTRS chart, subjective vision questionnaire, ophthalmoscopic examination, and SD OCT at 1, 3, 6 9, and 12 month visits; Demographics at Baseline; Medical History, Vital Signs and Physical Examination at Baseline; ECG, CBC, Chem 20 and HbA1C at Baseline; Dispense study medication at visits 2, 3, 4, 5, 6 and 7; Pill count at visits 3, 4, 5, 6 and 7; Non-directed assessment of adverse events at each visit, including classification as to severity, seriousness and body system. Concomitant medications at each visit. Statistics: Statistics will be generated for, at a minimum, , area of geographic atrophty, ETDRS visual acuity, central retinal thickness and presence of hemorrhage. Within patient trajectories for these outcomes will be plotted, incorporating information on dose and duration. Analysis of Variance may be conducted to relate logarithm of dose and duration of treatment to the outcomes listed above.

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