“Otilimab (GSK3196165) - Emerging Drug Insight and Market Forecast – 2030” the report provides comprehensive insights about an investigational product for Rheumatoid Arthritis in 7 Major Markets. A detailed picture of the OTILIMAB (GSK3196165) 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.
Overview
Otilimab (previously GSK3196165) is a fully human monoclonal antibody that inhibits granulocyte-macrophage colony-stimulating factor (GM-CSF), a protein that plays a central role in a broad range of immune-mediated diseases, including rheumatoid arthritis. GM-CSF acts on cells, including macrophages (an immune cell type that plays a key role in the inflammatory process), leading to inflammation, joint damage and pain. Otilimab neutralises the biological function of GM-CSF by blocking the interaction of GM-CSF with its cell surface receptor. In 2013 GSK assumed exclusive worldwide responsibility of otilimab from MorphoSys AG for all development and commercialisation activities in all therapeutic fields.
Scope of the report
The report provides insights into:

  • A comprehensive product overview including the product description, mechanism of action, dosage and administration, Research and Development activity.
  • Elaborated details on regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the drug research and development activity details across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around Otilimab (GSK3196165).
  • The report contains forecasted sales for Otilimab (GSK3196165) till 2030.
  • Comprehensive coverage of the late-stage emerging therapies (Phase III) for Rheumatoid Arthritis.
  • The report also features the SWOT analysis with analyst insights and key findings of Otilimab (GSK3196165).


Methodology
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.
Otilimab (GSK3196165) Analytical Perspective by DelveInsight

  • In-depth Otilimab (GSK3196165) Market Assessment


This report provides a detailed market assessment of Otilimab (GSK3196165) 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.

  • Otilimab (GSK3196165) Clinical Assessment


The report provides the clinical trials information of Otilimab (GSK3196165) covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

  • In the coming years, the market scenario for Rheumatoid Arthritis is set to change due to the extensive research and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
  • The companies and academics are working to assess challenges and seek opportunities that could influence Otilimab (GSK3196165) dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
  • Other emerging products for Rheumatoid Arthritis are giving market competition to Otilimab (GSK3196165) and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, development activities, and some key findings provide the current development scenario of Otilimab (GSK3196165).
  • Our in-depth analysis of the forecasted sales data of Otilimab (GSK3196165) from 2020 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Otilimab (GSK3196165).


Key Questions

  • Which company is developing Otilimab (GSK3196165) along with the phase of the clinical study?
  • What is the technology utilized in the development of Otilimab (GSK3196165)?
  • What is the product type, route of administration and mechanism of action of Otilimab (GSK3196165)?
  • What is the clinical trial status of the study and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Otilimab (GSK3196165) development?
  • What are the key designations that have been granted to Otilimab (GSK3196165)?
  • What is the forecasted market scenario of Otilimab (GSK3196165)?
  • What is the history of Otilimab (GSK3196165) and what is its future?
  • What is the forecasted sales of Otilimab (GSK3196165) in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
  • What are the other emerging products available and how these are giving competition to Otilimab (GSK3196165)?
  • Which are the late-stage emerging therapies under development for the treatment of the PPD?