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Clinical Trial Summary

This is a Phase I/II, multi-center, open-label proof-of-concept study of vamorolone. Twenty participants with a flare of mild or moderately active Ulcerative Colitis (defined as a Pediatric Ulcerative Colitis Activity Index [PUCAI] 10-60) will be enrolled and receive vamorolone 6 mg/kg/day orally once daily for 8 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04348890
Study type Interventional
Source ReveraGen BioPharma, Inc.
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date September 1, 2020
Completion date September 1, 2022

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