The purpose of this study is to evaluate the efficacy of DNK333 compared to placebo for relieving symptoms of IBS-D in female patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
180
Satisfactory relief of IBS-related abdominal pain/discomfort
Time frame: 4 weeks
Satisfactory relief of overall IBS-D symptoms
Time frame: 4 weeks
Occurrence and control of bowel urgency
Time frame: 4 weeks
Change in stool frequency
Time frame: 4 weeks
Severity of abdominal bloating
Time frame: 4 weeks
Severity of abdominal pain/discomfort
Time frame: 4 weeks
Safety
Time frame: 4 weeks
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Investigative Site
Tucson, Arizona, United States
Investigative Site
North Little Rock, Arkansas, United States
Investigative Site
Los Angeles, California, United States
Investigative Site
Orange, California, United States
Investigative Site
Riverside, California, United States
Investigative Site
Sacramento, California, United States
Investigative Site
San Diego, California, United States
Investigative Site
Colorado Springs, Colorado, United States
Investigative Site
Bristol, Connecticut, United States
Investigative Site
Hartford, Connecticut, United States
...and 33 more locations