{"id":390106,"date":"2021-02-15T00:00:00","date_gmt":"2021-02-15T00:00:00","guid":{"rendered":"https:\/\/clarivate.com\/life-sciences-healthcare\/report\/algoim0044-2021-biopharma-crohns-disease-treatment-algorithms-claims-data-analysis-pediatric-us-2021\/"},"modified":"2026-04-23T11:35:01","modified_gmt":"2026-04-23T11:35:01","slug":"algoim0044-2021-biopharma-crohns-disease-treatment-algorithms-claims-data-analysis-pediatric-us-2021","status":"publish","type":"report","link":"https:\/\/clarivate.com\/life-sciences-healthcare\/report\/algoim0044-2021-biopharma-crohns-disease-treatment-algorithms-claims-data-analysis-pediatric-us-2021\/","title":{"rendered":"Crohn&#8217;s Disease | Treatment Algorithms: Claims Data Analysis | Pediatric | US | 2021"},"content":{"rendered":"<p>Children with Crohn\u2019s disease (CD) have a more-complicated disease course compared with adult patients. However, similar to adult CD, the primary goal of the treatment of pediatric CD is to induce and maintain remission as quickly as possible. Historically, treatment of pediatric CD would begin with safe, albeit often less-efficacious, conventional agents (e.g., 5-ASAs) and then progress to more-potent drugs, such as biologics and\/or immunosuppressants. However, the pediatric CD treatment algorithm continues to evolve, and physicians increasingly initiate treatment with TNF-alpha inhibitors (e.g., Janssen\/Merck\u2019s Remicade, AbbVie\/Eisai\u2019s Humira), especially in patients with more-severe disease symptoms. The non-TNF biologics, including Takeda\u2019s Entyvio and Janssen\u2019s Stelara, may also be prescribed, particularly after anti-TNF failure.\u00a0<strong>QUESTIONS ANSWERED<\/strong><\/p>\n<ul>\n<li>What patient shares do key therapies and brands garner by line of therapy in newly diagnosed pediatric CD patients? What are the quarterly trends in prescribing among recently treated and newly diagnosed pediatric CD patients?<\/li>\n<li>How have Stelara and Entyvio been integrated into the treatment algorithm, and what are their sources of business?<\/li>\n<li>What percentage of pediatric CD patients receive drug therapy within 365 days of diagnosis, and how quickly? What percentage of patients progress to later lines of therapy within 365 days of diagnosis?<\/li>\n<li>What percentage of pediatric CD patients are treated with monotherapy versus combination therapy? What are the most commonly used combinations?<\/li>\n<li>What are the product-level compliance and persistency rates among drug-treated patients?<\/li>\n<\/ul>\n<p><strong>CONTENT HIGHLIGHTS<\/strong>\u00a0<strong>Geographies<\/strong>\u00a0United States\u00a0<strong>Real-World Data<\/strong>\u00a0Longitudinal patient-level claims data analysis\u00a0<strong>Key Drugs Covered<\/strong>\u00a0Humira, Remicade \/ biosimilar infliximab, Entyvio, Stelara, Cimzia, aminosalicylates, immunosuppressants\u00a0<strong>Key Analysis\u00a0<\/strong><strong>Provided<\/strong><\/p>\n<ul>\n<li>Brand\/therapy usage across longitudinal patient sample.<\/li>\n<li>Newly diagnosed patient analysis.<\/li>\n<li>Treatment initiation and progression.<\/li>\n<li>Line of therapy analysis.<\/li>\n<li>Combination therapy analysis.<\/li>\n<li>Source of business for recently treated patients.<\/li>\n<li>Persistency and compliance analysis.<\/li>\n<li>Product-level patient flowcharts.<\/li>\n<\/ul>\n<p><strong>PRODUCT DESCRIPTION<\/strong>\u00a0Treatment Algorithms: Claims Data Analysis provides detailed, quantitative analysis of the treatment journey and brand usage across lines of therapy and overall using real-world, patient-level claims data so that marketers can accurately assess their source of business, benchmark usage against competitors, and quantify areas of opportunity for their marketed or emerging brand.<\/p>\n","protected":false},"template":"","class_list":["post-390106","report","type-report","status-publish","hentry","report-gateway-biopharma","biopharma-therapy-areas-crohns-disease","biopharma-product-treatment-algorithms-claims-data-analysis","biopharma-geography-us","biopharma-date-950"],"acf":[],"publishpress_future_workflow_manual_trigger":{"enabledWorkflows":[]},"_links":{"self":[{"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/report\/390106","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/report"}],"about":[{"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/types\/report"}],"version-history":[{"count":1,"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/report\/390106\/revisions"}],"predecessor-version":[{"id":393231,"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/report\/390106\/revisions\/393231"}],"wp:attachment":[{"href":"https:\/\/clarivate.com\/life-sciences-healthcare\/wp-json\/wp\/v2\/media?parent=390106"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}