Market Research Report
GARETOSMAB (REGN2477)- Emerging Drug Insight and Market Forecast - 2030
|Published by||DelveInsight Business Research LLP||Product code||959710|
|Published||Content info||50 Pages
Delivery time: 1-2 business days
|GARETOSMAB (REGN2477)- Emerging Drug Insight and Market Forecast - 2030|
|Published: September 8, 2020||Content info: 50 Pages||
"GARETOSMAB (REGN2477)- Emerging Drug Insight and Market Forecast - 2030" the report provides comprehensive insights about an investigational product for Fibrodysplasia ossificans progressiva (FOP) in 7 Major Markets. A detailed picture of the GARETOSMAB (REGN2477) in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2020-2030 is provided in this report along with a detailed description of the product. The product details cover mechanism of action, dosage and administration, route of synthesis, and Research and development activity including regulatory milestones, and other development activities. Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.
Regeneron has been engaged in FOP research for over two decades and helped to provide fundamental insights in the biology and natural history of the disease. Regeneron scientists discovered that Activin A plays a key role in FOP by driving HO, the main pathology of FOP. Garetosmab is a VelocImmune-derived fully-human monoclonal antibody that binds and neutralizes Activin A, which is involved in the development of heterotopic bone in people with FOP. Garetosmab is currently being studied in adults with FOP. In 2017, the U.S. Food and Drug Administration (FDA) granted Fast Track designation for garetosmab for the prevention of HO in patients with FOP. In the U.S. and European Union (EU), garetosmab has been granted Orphan Designation. Garetosmab is currently under clinical development, and its safety and efficacy have not been evaluated by any regulatory authority
The report provides insights into:
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.
This report provides a detailed market assessment of GARETOSMAB (REGN2477) in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan. This segment of the report provides forecasted sales data from 2020 to 2030.
The report provides the clinical trials information of GARETOSMAB (REGN2477) covering trial interventions, trial conditions, trial status, start and completion dates.