The purpose of this study is to determine whether ATI-7505 is effective in the treatment of chronic idiopathic constipation.
This study is designed to evaluate the safety and efficacy of ATI 7505 in generally healthy, adult patients who have had symptoms of chronic idiopathic constipation for at least 6 months as defined in the ROME III criteria.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
214
Research Facility
Anaheim, California, United States
Research facility
Total number of spontaneous bowel movements during the first 7 days after randomization
Time frame: 7 days
Daily and/or weekly assessments of the consistency, severity, frequency, symptoms of constipation during the treatment period
Time frame: daily and or weekly
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80 mg ATI-7505, BID for 4 weeks
120 mg ATI-7505, BID, for 4 weeks
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Research Facility
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Research Facility
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Hollywood, Florida, United States
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South Miami, Florida, United States
Researrch Facility
Newnan, Georgia, United States
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Rockford, Illinois, United States
Research Facility
Evansville, Indiana, United States
...and 13 more locations