The purpose of this pilot, exploratory study is to evaluate the safety, tolerance, pharmacokinetics and potential activity of an investigational agent, HE3286, when administered orally, daily for 28 days to patients with mild-to-moderate ulcerative colitis.
HE3286 has a potentially new mechanism of action that may improve the current therapeutic options available to patients with ulcerative colitis. In preclinical experiments, HE3286 has shown activity in animal models of ulcerative colitis. Additionally, HE3286 has shown to have anti-inflammatory activity associated with corticosteroids but without the side effects associated with corticosteroid use, such as immune suppression and bone loss.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
27
Unnamed facility
Tucson, Arizona, United States
Unnamed facility
Anaheim, California, United States
Unnamed facility
Fresno, California, United States
Unnamed facility
La Jolla, California, United States
safety and pharmacokinetics
Time frame: duration of the study
assess activity on the signs and symptoms of active mild-to-moderate ulcerative colitis
Time frame: duration of the study
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Unnamed facility
Denver, Colorado, United States
Unnamed facility
Denver, Colorado, United States
Unnamed facility
Winter Park, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Louisville, Kentucky, United States
Unnamed facility
El Paso, Texas, United States