drugset / Trial / NCT04412785

Cyclosporine in Patients With Moderate COVID-19

NCT04412785

Phase 1 Completed 11 enrolled University of Pennsylvania
NaSingle-groupOpen-labelTreatment

Summary

Phase 1 safety study to determine the tolerability, clinical effects, and changes in laboratory parameters of short course oral or IV cyclosporine (CSA) administration in patients with COVID-19 disease requiring oxygen supplementation but not requiring ventilator support.

Timeline

Start
2020-06-30
Primary completion
2021-10-25
Completion
2021-10-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide 3 mg/kg Oral
Subject Cyclosporine Peptide 9 mg/kg Oral

Indications