drugset / Trial / NCT04326426

ODYSSEY: A Study to Investigate the Efficacy of Tradipitant in Treating Severe or Critical COVID-19 Infection

NCT04326426

Phase 3 Enrolling by invitation 300 enrolled Vanda Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, double-blind placebo-controlled trial to investigate the efficacy and safety of tradipitant 85 mg orally given twice daily to treat inflammatory lung injury associated with severe or critical COVID-19 infection. On evaluation for enrollment, participant will need to meet all inclusion and exclusion criteria. If participant consents, they will be randomized 1:1 to treatment with either tradipitant 85 mg PO BID or placebo in addition to standard of care for COVID-19 infection as per the protocol at the treating hospital. NEWS 2 will be assessed at screening and daily following randomization. Inflammatory lab markers as detailed should be collected once per day in the morning, preferably at the same time every morning. All enrolled participants will have whole blood collected for whole genome sequencing.

Timeline

Start
2020-04-13
Primary completion
2020-08-01
Completion
2020-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tradipitant Small molecule 85 mg Oral

Indications