Yes, Izervay, which is the brand name for avacincaptad pegol, received FDA approval on August 4, 2023. It is approved for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Izervay is specifically designed to treat geographic atrophy (GA), a severe form of age-related macular degeneration (AMD). Geographic atrophy is characterized by the progressive degeneration of the retina, which can lead to irreversible vision loss. Izervay helps slow down the progression of this condition, thereby preserving vision for a longer period.
Izervay works as a complement C5 protein inhibitor. In the case of geographic atrophy caused by AMD, an overactive complement system (part of the immune system) contributes to the damage and scarring of the retina. By inhibiting the complement protein C5, Izervay reduces the activity of the complement cascade, potentially slowing down the progression of retinal damage and geographic atrophy.
Effectiveness
Izervay is effective in slowing the progression of geographic atrophy secondary to AMD. By inhibiting the complement system, it helps maintain better vision over time.
Common side effects:
Serious side effects:
Patients are advised to call their doctor for medical advice about side effects and to report any adverse effects to the FDA at 1-800-FDA-1088.
Izervay, approved by the FDA on August 4, 2023, provides a crucial treatment option for patients with geographic atrophy secondary to age-related macular degeneration. By inhibiting the complement C5 protein, Izervay helps slow the progression of this vision-threatening condition, offering hope for better vision preservation.
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