Sun Hopes Cequa’s Nano Formulation Makes Big Impact

Sun’s now-approved higher concentration, quicker-acting formulation of cyclosporine A could offer competitive advantage in dry eye versus Allergan’s Restasis, but is it enough to offset lower costs of pending generic cyclosporines?

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Sun Pharmaceutical Industries Ltd. became the third company to gain US FDA approval of a drug for dry eye disease Aug. 16, as Cequa (cyclosporine ophthalmic solution 0.09%) was approved to increase tear production in patients suffering dry eye. At launch, expected to occur between October and next March, the drug will join Shire PLC’s Xiidra (lifitegrast) and Allergan PLC’s Restasis, also a cyclosporine A formulation, in the US dry eye market.

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