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Clinical Trial Summary

A randomized, multi-center, double-blind, three arm placebo-controlled study in male and non-pregnant, non-lactating female subjects aged 18 years to examine the safety and efficacy of two dosing regimens of hydrocortisone acetate 90 mg suppository administered with the Sephure applicator for the treatment of ulcerative colitis of the rectum.


Clinical Trial Description

Hydrocortisone acetate 90 mg or placebo will be administered as a rectal suppository with a Sephure suppository applicator. Two arms of the study will receive different dosage regimens of hydrocortisone acetate, and the third arm will receive placebo. All subjects will administer the study drug twice a day; once in the morning and once in the evening for 28 days. The study population will consist of male and non pregnant, non lactating females aged 18 years and older with a confirmed diagnosis of active UC of the rectum. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04469686
Study type Interventional
Source Cristcot LLC
Contact Mark C Ensign
Phone 978-212-6380
Email mark.ensign@cristcot.com
Status Recruiting
Phase Phase 3
Start date December 10, 2020
Completion date June 30, 2024

See also
  Status Clinical Trial Phase
Terminated NCT03521232 - A Study of Niclosamide Enemas in Subjects With Active Ulcerative Proctitis or Ulcerative Proctosigmoiditis Phase 1/Phase 2