The purpose of this study is to determine the safety and efficacy of 2 doses of ABT-874 versus placebo in the treatment of subjects with moderate to severe plaque psoriasis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
1,465
PGA
Time frame: Proportion of subjects achieving a PGA 0/1 (Clear or minimal) at Week 12
PASI
Time frame: Subjects achieving a PASI 75 response defined as a 75% reduction in the PASI score from baseline at Week 12
PGA
Time frame: Proportion of subjects maintaining a PGA 0/1 response at Week 52
DLQI
Time frame: Change from Baseline in DLQI total score vs. placebo at Week 12
NAPSI
Time frame: % change in NAPSI score at Week 12 vs placebo in subjects with nail psoriasis
PASI
Time frame: Subjects who achieve PASI 90 and 100 at Week 12
Safety parameters
Time frame: Throughout study
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Site Reference ID/Investigator# 6579
Birmingham, Alabama, United States
Site Reference ID/Investigator# 6697
Birmingham, Alabama, United States
Site Reference ID/Investigator# 7015
Huntsville, Alabama, United States
Site Reference ID/Investigator# 6728
Scottsdale, Arizona, United States
Site Reference ID/Investigator# 6584
Tucson, Arizona, United States
Site Reference ID/Investigator# 6696
Little Rock, Arkansas, United States
Site Reference ID/Investigator# 6591
Bakersfield, California, United States
Site Reference ID/Investigator# 6710
Fresno, California, United States
Site Reference ID/Investigator# 7885
Irvine, California, United States
Site Reference ID/Investigator# 6872
Los Angeles, California, United States
...and 106 more locations