EYSUVIS™ (KPI-121 0.25%)

Dry Eye Disease

Quarterly Sales (Approved)

Exp Date

February 05, 2021 (Est)

Amp Volatility Score


Catalyst Info & Data Links


  • EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25% is approved for the short-term (up to two weeks) treatment of the signs and symptoms of dry eye disease. EYSUVIS utilizes Kala's AMPPLIFY mucus-penetrating particle (MPP) Drug Delivery Technology to enhance penetration of loteprednol etabonate (LE) into target tissue of the ocular surface. EYSUVIS was approved by the FDA on October 26, 2020. Kala believes that EYSUVIS' broad mechanism of action, rapid onset of relief of both signs and symptoms, favorable tolerability and safety profile and the potential to be complementary to existing therapies, offer a differentiated product profile for the management of dry eye flares. A link to the full product label can be found at: www.eysuvis.com.



Updated by HC

#KALA, #EYSUVIS,  #KPI-121 0.25%, #Dry Eye Disease, #tears

Prior Data (click to view full image)


Trial Design / Revenue (click to view full image)


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Summary: Obtained FDA Approval for EYSUVISTM, First Prescription Therapy Approved Specifically for the Short-Term Treatment of the Signs and Symptoms of Dry Eye Disease EYSUVIS Expected to Begin Ship...

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