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POS1031 (2021) : LOW INCIDENCE OF GASTROINTESTINAL-RELATED AND OVERALL SERIOUS ADVERSE EVENTS AMONG GUSELKUMAB-TREATED PATIENTS: POOLED ANALYSES OF VOYAGE 1 & 2 AND DISCOVER 1 & 2 THROUGH 1-YEAR

Researchers

Presenter

  • P. J. Mease

Principal Investigators

  • P. Foley

  • K. Reich

  • M. Lebwohl

  • Y. W. Yang

  • M. Shawi

  • M. Miller

  • A. Kollmeier

  • E. C. Hsia

  • X. L. Xu

  • P. Ramachandran

  • S. Sheng

  • Y. You

  • P. Helliwell

  • W. H. Boehncke

Medical Centers

  • 2Swedish Medical Center/Providence St. Joseph Health and University of Washington, Rheumatology, Seattle, Washington, United States of America

  • The University of Melbourne, St. Vincent’s Hospital Melbourne and Probity Medical Research, Skin Health Institute, Department of Medicine, Carlton, Australia

  • University Medical Center Hamburg-Eppendorf, Translational Research in Inflammatory Skin Diseases, Institute for Health Services Research in Dermatology and Nursing, Hamburg, Germany

  • Psoriasis Treatment Center of Central New Jersey, Department of Dermatology, East Windsor, United States of America

  • Icahn School of Medicine at Mount Sinai, Department of Health Evidence and Policy, New York, United States

  • , Janssen Global Services, LLC, Horsham, PA, United States of America

  • Janssen Research & Development, Raritan, United States of America

  • Janssen Research & Development, LLC, Immunology, San Diego, CA, United States of America

  • University of Pennsylvania School of Medicine, Immunology, Philadelphia, United States of America

  • Janssen Research & Development, Raritan, United States of America

  • University of Leeds, Leeds Institue of Rheumatic and Musculoskeletal Medicine, Leeds, United Kingdom

Locations

  • United States

  • Australia

  • Germany

  • United Kingdom

  • Switzerland

Companies

  • N/A

Study Components

Therapeutic Area

  • Ophthalmology (OP)

Disease

  • Uveitis

Biomarkers

  • N/A

Drug/Treatment

  • guselkumab (IV)

Outcome

  • N/A


Study Design

  • Placebo Control

  • Controlled

Phase

  • III

Study Id's

  • N/A

Sponsors

  • Abbvie

Result

  • N/A