A Clinical Study Report (CSR) Summary is a document that summarizes a full CSR, providing a high-level overview of the study plan and results, including a numerical summary of efficacy and safety results, study objective(s), criteria for inclusion, methodology, etc. Data Partners have committed to making CSR Summaries available as quickly as possible. Some CSR Summaries are already available on the Trials page. Others may be available through either Health Canada or the EMA. If you are interested in a CSR Summary that is not listed on the Trials page nor at EMA or Health Canada, please use the form below to request it. First Name * Last Name * Email Address * NCT # (preferred) If the NCT # is unknown, please provide another identifier, such as the PMID #, ICTRP #, or other biomedical literature citation # Notes: NCT # is the unique identifier from the National Institutes of Health ClinicalTrials.gov database. PMID # is the unique identifier from the National Library of Medicine’s PubMed database. ICTRP # is the unique identifier from the World Health Organization's International Clinical Trials Registry Platform. If you provide a unique identifier from another database, please be specific. Additional trial-specific information
