FDA Approves Vanda Pharmaceuticals' NEREUS for Motion Sickness Prevention

Reuters

Dec 31, 2025

FDA Approves Vanda Pharmaceuticals' NEREUS for Motion Sickness Prevention

Vanda Pharmaceuticals Inc. has received approval from the U.S. Food and Drug Administration (FDA) for NEREUS™ (tradipitant), an oral neurokinin-1 (NK-1) receptor antagonist, for the prevention of vomiting induced by motion. This marks the first new pharmacologic treatment for motion sickness in over 40 years, representing a significant advancement in the management of this condition. Vanda plans to launch NEREUS™ in the coming months and is also exploring its potential in other conditions related to nausea and vomiting.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Vanda Pharmaceuticals Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: PH54898) on December 30, 2025, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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