-Allergan Inc. announced on Tuesday that it received approval from the US Food and Drug Administration (FDA) to market Restasis (cyclosporine ophthalmic emulsion, 0.05%) to patients with keratoconjunctivitis sicca (KCS).
Allergan said the FDA approval was based on a phase III study, demonstrating that use of Restasis resulted in clinically relevant increases in Schirmer wetting versus other potential treatments such as topical anti-inflammatory drugs or using punctal plugs.
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