Status:

COMPLETED

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

Lead Sponsor:

Vanda Pharmaceuticals

Conditions:

Motion Sickness

Eligibility:

All Genders

18-75 years

Phase:

PHASE2

Brief Summary

Randomized, double-blind, placebo-controlled investigating the efficacy of tradipitant in the treatment of motion sickness.

Eligibility Criteria

Inclusion

  • Male or non-pregnant, non-lactating female patients aged 18 - 75 years (inclusive);
  • Body Mass Index (BMI) of ≥18 and \<40 kg/m2;
  • History or symptoms consistent with motion sickness

Exclusion

  • Chronic nausea due to condition other than motion sickness;
  • A positive test for drugs of abuse at the screening or evaluation visits;
  • Clinically significant deviation from normal clinical laboratory results

Key Trial Info

Start Date :

December 20 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 27 2019

Estimated Enrollment :

126 Patients enrolled

Trial Details

Trial ID

NCT03772340

Start Date

December 20 2018

End Date

June 27 2019

Last Update

May 9 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Vanda Investigational Site

Santa Monica, California, United States, 90404

Motion Sifnos: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness | DecenTrialz