Ilaris - Drug Insight and Market Forecast - 2030

“Ilaris- Drug Insight and Market Forecast - 2030” report outlays comprehensive insights of the product indicated for the treatment of its approved condition. A detailed picture of the Ilaris in Seven Major Markets, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2017-2030 is provided in this report along with a detailed description of the product. The product details covers mechanism of action, dosage and administration, route of synthesis, and pharmacological studies, including product marketed details, regulatory milestones, and other development activities. Further, it also consists of market assessments inclusive of the market forecast, SWOT analysis, and detailed analyst views. It further highlights the market competitors, late-stage emerging therapies, and patent details in the global space.

Drug Summary
Canakinumab, sold under the brand name Ilaris is a medication for the treatment of systemic juvenile idiopathic arthritis and active Still's disease, including adult-onset Still's disease. It is a human monoclonal antibody targeted at interleukin-1 beta.

In June 2020, Novartis ILARIS (canakinumab) received US Food and Drug Administration (FDA) approval for a new indication to treat Adult-Onset Still's Disease (AOSD)1. The FDA granted an indication for active Still's disease including both systemic juvenile idiopathic arthritis (SJIA) and AOSD in patients aged 2 years and older.

Scope of the Report

The report provides insights into:

• A comprehensive product overview including the product description, mechanism of action, dosage and administration, route of synthesis, pharmacological studies (pharmacodynamics and pharmacokinetics) and adverse reactions.
• Elaborated details on regulatory milestones and other development activities have been provided in this report.
• The report also highlights the drug marketed details across the United States, Europe and Japan.
• The report also covers the patents information with expiry timeline around Ilaris.
• The report contains historical and forecasted sales for Ilaris till 2030.
• Comprehensive coverage of the late-stage emerging therapies (Phase III) in the space with a brief snapshot of the details.
• The report also features the SWOT analysis with analyst insights and key findings of Ilaris.

Methodology

The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by the research 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.

Ilaris Analytical Perspective

In-depth Ilaris Market Assessment

This report provides a detailed market assessment of Ilaris 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 historical and forecasted sales data from 2017 to 2030.

Ilaris Clinical Assessment

The report provides the clinical trials information of Ilaris covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

• In the coming years, the market scenario for Ilaris is set to change due to the extensive research in the treatment of the indicated condition 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 Ilaris dominance. The therapies under development are focused on novel approaches to treat/improve the disease condition.
• Other approved products for the disease are giving market competition to Ilaris 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 market scenario of Ilaris.
• The in-depth analysis of the sales data of Ilaris from 2017 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Ilaris in the market.

Key Questions Answered

• What is the prescribed dosage and strengths of Ilaris are available in the market?
• What are the common adverse reactions or side effects of Ilaris?
• What is the product type, route of administration and mechanism of action of Ilaris?
• What are the chemical specifications of Ilaris?
• How are the clinical trials diversified on the basis of the trial status?
• What is the history of Ilaris, and what is its future?
• What are the marketed details of Ilaris in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
• How many patents have been granted to Ilaris and when these patents will get expire?
• What are the pros (benefits) and cons (disadvantages) of Ilaris?
• In which countries Ilaris got approval and when it gets launched?
• What are the clinical trials are currently ongoing for Ilaris?
• How the safety and efficacy results determined the approval of Ilaris?
• What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Ilaris development?
• What are the key designations that have been granted to Ilaris?
• What is the historical and forecasted market scenario of Ilaris?
• How is the market trend of Ilaris is different in the Seven Major Markets (the United States, EU5 [Germany, France, Italy, Spain, and the United Kingdom], and Japan)?
• What are the other approved products available and how these are giving competition to Ilaris?
• Which are the late-stage emerging therapies under development for the treatment of the indicated condition?