Paroxetine and Pediatric and Adolescent Clinical Trial Data
Overview
GlaxoSmithKline has conducted a series of clinical studies to determine the efficacy and safety of paroxetine in treating children and adolescent patients with major depressive disorder, obsessive compulsive disorder and social anxiety disorder/social phobia. In the interest of further making the results of these studies available to all interested parties, GSK is posting to this Web page the following documents:
Clinical Study Reports
These are the formal study reports, which are the basis of submissions to the FDA, EMEA, MHRA and other regulatory agencies for all the studies of paroxetine in children and adolescents. They are presented here in two parts, the report Synopses, and the Full Reports (text and associated tables). [Because their size is many hundreds of pages, the appendices, which include line listings of raw data, the original protocol and its amendments, records of IRB approvals, etc., are not included. Names of investigators and sites have been redacted to preserve confidentiality.]
Bibliography of publications
This is a list of all the publications in peer-reviewed journals and poster presentations at scientific meetings which have been derived from
GSK-sponsored studies of paroxetine in adolescents and children.
Medical Information Letter
This letter is sent to healthcare professionals in the United States who request information about paroxetine and its use in children and/or adolescents.
Paroxetine has not been approved in Europe or North America for the treatment of patients younger than 18 years of age.