Kala Pharmaceuticals Inc. is planning to file a new drug application in the US for what it hopes will become the first FDA-approved treatment for short-term dry eye disease, specifically dry eye flares. The $1.7bn dry eye market is currently dominated by Shire PLC and Allergan PLC, with Xiidra (lifitegrast) and Restasis (cyclosporine ophthalmic emulsion) respectively.
While the New Drug Application (NDA) for KPI-121 0.25% (loteprednol etabonate) will be based on existing clinical studies, STRIDE 1...







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