To compare the efficacy, safety and pharmacokinetics of ABT-874 to placebo in subjects who have moderately to severely active Crohn's Disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
246
Proportion of subjects achieving clinical remission, defined as CDAI score of <150 points
Time frame: Week 6
Patient reported outcomes, clinical response indicators, safety parameters
Time frame: Weeks 12 and 24
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Site Ref # / Investigator 6792
Orange, California, United States
Site Ref # / Investigator 6643
San Diego, California, United States
Site Ref # / Investigator 6670
Hamden, Connecticut, United States
Site Ref # / Investigator 6694
Gainesville, Florida, United States
Site Ref # / Investigator 6794
Jacksonville, Florida, United States
Site Ref # / Investigator 6687
Winter Park, Florida, United States
Site Ref # / Investigator 6667
Zephyrhills, Florida, United States
Site Ref # / Investigator 6691
Atlanta, Georgia, United States
Site Ref # / Investigator 6642
Atlanta, Georgia, United States
Site Ref # / Investigator 8797
Macon, Georgia, United States
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