drugset / Trial / NCT04379271

A Study to Evaluate the Efficacy, Safety and Tolerability of IMU-838 as Addition to Investigator's Choice of Standard of Care Therapy, in Patients With Coronavirus Disease 19 (COVID-19)

NCT04379271

Phase 2/3 Completed 234 enrolled Immunic AG FGK Clinical Research GmbH · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

At present there is no approved drug treatment for Covid-19. In this study we plan to investigate if an experimental drug called IMU-838 (vidofludimus calcium) can improve your symptoms, prevent worsening that would initiate further treatments such as ventilation, and can lower your virus number if given in addition to your doctor's choice of standard therapy. We will also test if IMU-838 has any side effects and measure the level of IMU 838 in your blood. Experimental drug means that it is not yet authorized for marketing in your country. To date approximately 600 individuals have received IMU-838 (or a drug similar to IMU-838 that contains the same active substance as IMU-838) in research studies.

Timeline

Start
2020-06-11
Primary completion
2021-01-12
Completion
2021-02-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Vidofludimus Small molecule 22.5 mg Oral

Indications