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The FDA has lifted the partial clinical hold on Vanda Pharmaceuticals' motion sickness drug tradipitant, allowing the company to extend clinical studies and eliminating the need for an additional six-month dog toxicity study. The FDA agreed with Vanda's position that motion sickness is an acute, self-limiting physiologic response rather than a chronic or chronic-intermittent condition. The ongoing review of tradipitant's new drug application for motion sickness prevention remains on track.
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