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A Randomized, Double-Blind, Placebo-Controlled, 4-week Trial of IMO-3100 in Patients With Moderate to Severe Plaque Psoriasis
The purpose of this study is to evaluate different dose levels of IMO-3100 compared to placebo administered for 4 weeks to patients with moderate to severe plaque psoriasis.
To evaluate the safety, tolerability and treatment effect of different dose levels of IMO-3100 compared to placebo administered for 4 weeks to patients with moderate to severe plaque psoriasis.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Florida Center for Dermatology, P.A
Jacksonville, Florida, United States
Atlanta Dermatology, Vein & Research Center, PC
Alpharetta, Georgia, United States
Dermatologic Surgery Specialists, Inc.
Macon, Georgia, United States
Indiana Clinical Trials Center, PC
Plainfield, Indiana, United States
DermResearch PLLC
Louisville, Kentucky, United States
Tufts Medical Center
Boston, Massachusetts, United States
Mass General Hospital Clinical Unit for Research Trials in Skin
Boston, Massachusetts, United States
Derm Research Center of New York
Stony Brook, New York, United States
Oregon Dermatology and Research Center
Portland, Oregon, United States
Clinical Partners, Inc
Johnston, Rhode Island, United States
Start Date
May 1, 2012
Primary Completion Date
November 1, 2012
Completion Date
December 1, 2012
Last Updated
January 9, 2018
44
ACTUAL participants
IMO-3100 at 0.16 mg/kg
DRUG
Saline for Injection
DRUG
IMO-3100 at 0.32 mg/kg
DRUG
Lead Sponsor
Idera Pharmaceuticals, Inc.
NCT06888193
NCT07234591
Data Source & Attribution
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