US FDA approves Cystadrops

26 August 2020
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Recordati Rare Diseases, a subsidiary of Italy’s Recordati Farmaceutici (RECI: MI), says that the US Food and Drug Administration (FDA) has approved Cystadrops (cysteamine ophthalmic solution) 0.37%.

Cystadrops is a new, viscous eye drop solution that depletes corneal cystine crystal deposits in people living with cystinosis.

Cystadrops demonstrated a significant reduction in cystine crystal deposits in the cornea of the eye and is the first and only FDA-approved cysteamine drop formulation with four times a day dosing. Cystinosis is a rare genetic condition present from birth that leads to the build-up of cystine crystals throughout the body, causing widespread tissue and organ damage and significant impact on the eyes.

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