This study will evaluate the tolerability, safety and efficacy of DNK333 against diarrhea caused by Irritable Bowel Syndrome in women.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
135
25 mg and 100 mg oral doses, each taken twice daily
Unnamed facility
Anniston, Alabama, United States
Change from baseline in average stool form score at 2 weeks
Time frame: 2 weeks
Change from baseline in average score at week 1, week 2: Abdominal pain/discomfort, bloating; satisfaction with bowel habits; weekly stool frequency; percent of days with satisfactory control of bowel urgency; satisfactory relief of overall IBS symptoms
Time frame: 2 weeks
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Unnamed facility
Huntsville, Alabama, United States
Unnamed facility
Northport, Alabama, United States
Unnamed facility
Tucson, Arizona, United States
Unnamed facility
North Little Rock, Arkansas, United States
Unnamed facility
Orange, California, United States
Unnamed facility
Riverside, California, United States
Unnamed facility
San Diego, California, United States
Unnamed facility
Torrance, California, United States
Unnamed facility
Bristol, Connecticut, United States
...and 19 more locations