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Vanda Pharmaceuticals Reports Results from a Phase III study of Tradipitant in Motion Sickness

WASHINGTON, May 25, 2023 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced the results from its Phase III study of tradipitant

articleVanda Pharmaceuticals Inc.May 25, 20235/company/vanda-pharmaceuticals-inc/news/vanda-pharmaceuticals-reports-results-from-a-phase-iii-study-of-tradipitant-in-motion
Vanda Pharmaceuticals Reports Results from a Phase III study of Tradipitant in Motion Sickness

About this update from Vanda Pharmaceuticals Inc.

[{"type":"text","content":"WASHINGTON, May 25, 2023 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced the results from its Phase III study of tradipitant in motion sickness, confirming the previously reported results demonstrating that tradipitant is effective in the prevention of vomiting associated with motion sickness. The Phase III study was conducted in real-world conditions on boats in the coastal waters of the United States (U.S.).\nThe Motion Syros study was a multicenter, randomized, double-blind, placebo-controlled study where 365 participants embarked on boat trips under varied sea conditions and received tradipitant 170 mg, tradipitant 85 mg, or placebo. Study participants had a prior history of motion sickness and were distributed across thirty-four boat trips that took place between November 2021 and April 2023. Sea conditions and participant evaluation of the symptoms of motion sickness were recorded for each trip. The primary endpoint of the study was the effect of tradipitant on vomiting induced by motion sickness.\nBoth 170 mg and 85 mg tradipitant doses were shown to be superior to placebo in preventing vomiting with only 18.3% and 19.5% of participants experiencing vomiting on tradipitant 170 mg and 85 mg respectively, as compared to 44.3% of participants on placebo (p \nMotion sickness remains an unmet need as various pharmacological and non-pharmacological interventions suffer from low efficacy, substantial side effects, or both. The U.S. Food and Drug Administration (FDA) has not approved a new medication for motion sickness in over forty years, since the approval of scopolamine, a transdermal patch placed behind the ear, in 1979.\nVanda plans to continue the motion sickness clinical program and pursue FDA approval upon completion of additional efficacy and safety studies.\nTable 1: Results of Motion Syros study for the Overall population across all sea conditions\n% Vomiting\nDifference v. Placebo\nP-value\nTradipitant 170 mg\nn=120\n18.3 %\n26.0 %\n\nTradipitant 85 mg\nn=123\n19.5 %\n24.8 %\n\nPlacebo\nn=122\n44.3 %\n \nMotion sickness\nMotion sickness is a disorder characterized by a constellation of symptoms, with nausea and vomiting being the primary ones1. Motion sickness has plagued travelers for thousands of years, as evidenced by the ancient Greek physician Hippocrates who wrote \"sailing on ...

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