drugset / Trial / NCT04169061

Impact of Acthar on Everyday Life of Participants With Severe Keratitis

NCT04169061

Phase 4 Completed 36 enrolled Mallinckrodt
NaSingle-groupOpen-labelTreatment

Summary

We will need about 36 participants for this study. Volunteers might be able to participate if: * they have bad noninfectious keratitis * early treatments failed or were not well tolerated Participants will be in the study for about 22 weeks: * 4 weeks for tests to see if the study might be good for them * 12 weeks of treatment with Acthar gel * 4 weeks to wean off Acthar gel and follow-up with the doctor

Timeline

Start
2019-11-13
Primary completion
2020-11-09
Completion
2020-12-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Acthar Peptide 80 iu Subcutaneous

Indications