This trial will evaluate the effect of ASP7147 on daily abdominal pain due to IBS-D during 4 weeks of treatment. It will also evaluate safety and tolerability in patients with IBS-D over the 4-week treatment period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
64
Elite Clinical Studies
Phoenix, Arizona, United States
Shahram Jacobs, M.D., Inc.
Encino, California, United States
Grossmont Center for Clinical Research
La Mesa, California, United States
Abdominal pain
10-point pain scale
Time frame: 4 weeks
Stool consistency
Bristol Stool Scale (7-point scale)
Time frame: 4 weeks
Stool frequency
Number of bowel movements per day
Time frame: 4 weeks
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