Allergan and Serenity receive FDA approval for Noctiva

6 March 2017
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Dublin, Ireland-headquartered Allergan (NYSE: AGN) and American specialty pharmaceutical company Serenity Pharmaceuticals have received approval from the US Food and Drug Administration for Noctiva (desmopressin acetate).

The nasal spray, a treatment for nocturnal polyuria, a condition characterized by overproduction of urine at night, has been indicated for use by adults who awaken at least twice nightly for micturition.

The FDA approval is based on two randomized clinical trials involving over 1,000 patients which found more patients treated with desmopressin experienced at least half as many night-time urinations compared with those in the placebo group.

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