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Administration of Hydroxychloroquine (Plaquenil) to African Americans and Hispanics for the Treatment of Mild to Severe Ulcerative Colitis
Sponsor: Icahn School of Medicine at Mount Sinai
Summary
The objective of this study is to assess the efficacy of hydroxychloroquine (HCQ) when combined with Mesalamine in reducing clinical and histologic disease activity in patients who have active mild to severe Ulcerative Colitis (UC) and also to assess the immunological effects of hydroxychloroquine in this population. These outcomes will be evaluated both clinically and experimentally. In vitro, flow cytometry will be employed to measure the expression of CTLA-4 on activated CD4+CD25+CD127- Tregs from patients prior to treatment with HCQ, and then at the end of a 4 month follow up period. Suppression assays will be used to determine the functional capacity of the patient derived Tregs. Clinically, patients will be monitored for remission as defined by reduction in patient reported stool frequency and rectal bleeding (mayo sub-score 0 or 1) and endoscopically, by improvement in mucosal appearance (mayo sub-score 0 or 1), all objective measures in the mayo score.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
3
Start Date
2022-06-10
Completion Date
2025-05
Last Updated
2025-02-11
Healthy Volunteers
No
Conditions
Interventions
Hydroxychloroquine
400mg of hydroxychloroquine per oral daily
Mesalamine
the participant will maintain their current standard of care dose which can range from 1.5g to 4.8g of mesalamine per oral daily
Locations (2)
Emory University School of Medicine
Atlanta, Georgia, United States
Icahn School of Medicine at Mount Sinai/Mount Sinai Hospital
New York, New York, United States