Ixekizumab is a humanized immunoglobulin G subclass 4 (IgG4) monoclonal antibody (mAb) against interleukin-17A (IL-17A) and prevents it from interacting with the IL-17A receptor. As IL-17A is a pro-inflammatory cytokine involved in inflammation and immune responses, blocking its effect is beneficial for use in inflammatory conditions. In particular, IL-17A h...
Ixekizumab is indicated for the treatment of patients aged six years or older with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. It is also indicated in adult patients with active psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis with objective signs of inflammation.
Northwestern University, Chicago, Illinois, United States
Modern Research Associates PLLC, Dallas, Texas, United States
Hospital Univ. Dr. Jose Eleuterio Gonzalez, Monterrey, Nuevo León, Mexico
Anaheim Clinical Trials, LLC, Anaheim, California, United States
Avail Clinical Research LLC, DeLand, Florida, United States
High Point Clinical Trials Center, High Point, North Carolina, United States
Institute of Arthritis Research, Idaho Falls, Idaho, United States
TriWest Research Assocaites, El Cajon, California, United States
Desert Medical Advances, Palm Desert, California, United States
Modern Research Associates PLLC, Dallas, Texas, United States
Menter Dermatology Research Institute, Dallas, Texas, United States
Tufts Medical Center, Boston, Massachusetts, United States
Klein and Associates MD, PA, Hagerstown, Maryland, United States
Marietta Rheumatology, Marietta, Georgia, United States
Sarasota Arthritis Center, Sarasota, Florida, United States
Rheumatology Center of San Diego, Escondido, California, United States
Care Access Research - Huntington Beach, Huntington Beach, California, United States
Arthritis Assoc. & Osteoporosis Ctr of Colorado Springs, LLC, Colorado Springs, Colorado, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Ulm, Germany
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Kiel, Germany
Heartland Research Associates, Wichita, Kansas, United States
University of California, Davis - Health Systems, Sacramento, California, United States
Robert A. Harrell, III, MD, Durham, North Carolina, United States
For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician., Toronto, Canada
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Salford, United Kingdom
Covance, Dallas, Texas, United States
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