Motion Syros: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness

Last updated: November 19, 2024
Sponsor: Vanda Pharmaceuticals
Overall Status: Completed

Phase

3

Condition

Vomiting

Treatment

Tradipitant

Placebo

Clinical Study ID

NCT04327661
VP-VLY-686-3401
  • Ages 18-75
  • All Genders

Study Summary

A multi-center, randomized, double-blind, placebo-controlled study to investigate the efficacy of tradipitant in subjects affected by motion sickness during travel

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • History of motion sickness

  • Age 18-75

Exclusion

Exclusion Criteria:

  • Nausea-inducing disorder other than motion sickness

  • BMI>40

  • History of intolerance and/or hypersensitivity to Neurokinin-1 Receptor antagonists

Study Design

Total Participants: 366
Treatment Group(s): 2
Primary Treatment: Tradipitant
Phase: 3
Study Start date:
November 15, 2021
Estimated Completion Date:
April 12, 2023

Connect with a study center

  • Pacific Research Network, LLC

    San Diego, California 92103
    United States

    Site Not Available

  • Pacific Research Partners

    San Diego, California 94607
    United States

    Site Not Available

  • Santa Monica Clinical Trials

    Santa Monica, California 90025
    United States

    Site Not Available

  • Gulfcoast Psychiatric Associates

    Fort Myers, Florida 33912
    United States

    Site Not Available

  • Harmony Clinical Research

    North Miami Beach, Florida 33162
    United States

    Site Not Available

  • Avita Clinical Research

    Tampa, Florida 33613
    United States

    Site Not Available

  • Beacon Clinical Research

    Boston, Massachusetts 02169
    United States

    Site Not Available

  • Beacon Clinical Research

    Quincy, Massachusetts 02169
    United States

    Site Not Available

  • Manhattan Medical Research

    New York, New York 10016
    United States

    Site Not Available

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