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Kowa Company Ltd.
New Drug Application for “K-911” Targeting Patients with Glaucoma and Ocular Hypertension Accepted for Filing in the U.S., Food and Drug Administration
August 27, 2026
Selective PPARα Modulator “K-808” (Pemafibrate) Granted “Breakthrough Therapy” Designation by the U.S. Food and Drug Administration (FDA) As a Treatment for Primary Biliary Cholangitis
June 30, 2026