drugset / Trial / NCT05903924

Motion Serifos: A Study to Investigate the Efficacy of Tradipitant in Participants Affected by Motion Sickness

NCT05903924 ↗

Phase 3 Completed 316 enrolled Vanda Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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

Timeline

Start
2023-09-09
Primary completion
2024-04-06
Completion
2024-04-24

Outcome

Met primary endpoint

paper 10.4% of the 170-mg tradipitant group and 18.3% of the 85-mg tradipitant group experienced vomiting, compared with 37.7% of the placebo group PMID 42150111 ↗

paper P = 0.00002 and P = 0.0014, respectively PMID 42150111 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tradipitant Small molecule 85 mg Oral
Subject Tradipitant Small molecule 170 mg Oral

Indications