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PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV

PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV

PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV

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Poster Psoriasis<br />

P 37<br />

MK-3222, an anti-IL23p19 antibody, is safe and effective in the treatment of<br />

psoriasis<br />

Tamara Kopp 1<br />

Elisabeth Riedl 2<br />

Christine Bangert 1<br />

Eli Greisenegger 1<br />

Ann Horowitz 3<br />

Thomas Marbury 4<br />

Robert Stonerock 4<br />

Victor Vidals 5<br />

Jonathan Dosik 6<br />

Claus Zachariae 7<br />

Norbert Reider 8<br />

Alan J Kivitz 9<br />

Danlin Xu 3<br />

Xiaoli Shirley Hou 3<br />

A.S. Zandvliet 3<br />

Matias Morrison 3<br />

Sauzanne Khalilieh 3<br />

1 Department of Dermatology, Division of Immunology, Allergy & Infectious Diseases,<br />

University of Vienna Medical School, Vienna, Austria<br />

2 Department of Dermatology, Division of General Dermatology, University of Vienna<br />

Medical School, Vienna, Austria<br />

3 Merck& Co., Inc., White House Station NJ, USA<br />

4 Orlando Clinical Research Center, Orlando, FL, USA<br />

5 PRA Lenexa, Kansas, USA<br />

6 TKL Research, Inc. Paramus, NJ, USA<br />

7 Department of Dermatology, Gentofte Hospital, University of Copenhagen, Denmark<br />

8 Deptartment of Dermatology, Medical University of Innsbruck, Innsbruck, Austria<br />

9 Altoona Center for Clinical Research Duncansville, PA, USA<br />

Introduction & Objectives: Psoriasis is a chronic inflammatory skin disorder affecting<br />

approximately 2% of people worldwide. The goal of therapy is clearance of psoriatic<br />

plaques. The benchmark response in most clinical trials is a 75% or greater reduction<br />

from the baseline PASI score. Recent discoveries have demonstrated that IL-23dependent<br />

Th17 cells control much of the inflammatory injury that is observed in<br />

diseases such as psoriasis. The safety and efficacy of the anti-IL23p19 antibody,<br />

MK-3222, was assessed in psoriasis.<br />

Materials & Methods: This was a randomized, double-blind, placebo-controlled,<br />

parallel-group dose-ranging, 3-Part, study which evaluated the safety, tolerability,<br />

91

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