Upadacitinib- Drug Insight and Market Forecast – 2030

“Upadacitinib- Drug Insight and Market Forecast – 2030” report by DelveInsight outlays comprehensive insights of the product indicated for the treatment of its approved condition. A detailed picture of the Upadacitinib 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.

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Drug Summary
Upadacitinib, sold under the brand name Rinvoq, is a Janus kinase (JAK) inhibitor medication for the treatment of moderately to severely active rheumatoid arthritis in adults where methotrexate (a drug used to treat active arthritis) did not work well or could not be tolerated. It was approved for medical use in the United States and in the European Union in 2019, and was developed by the biotech company AbbVie. Upadacitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adults who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (DMARDs).[4] Upadacitinib may be used as monotherapy or in combination with methotrexate.
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 Upadacitinib.
• The report contains historical and forecasted sales for Upadacitinib 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 Upadacitinib.

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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.
Upadacitinib Analytical Perspective by DelveInsight
• In-depth Upadacitinib Market Assessment
This report provides a detailed market assessment of Upadacitinib 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.

• Upadacitinib Clinical Assessment
The report provides the clinical trials information of Upadacitinib covering trial interventions, trial conditions, trial status, start and completion dates.
Report highlights
• In the coming years, the market scenario for Upadacitinib 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 Upadacitinib 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 Upadacitinib 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 Upadacitinib.
• Our in-depth analysis of the sales data of Upadacitinib from 2017 to 2030 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the Upadacitinib in the market.
Key Questions
• What is the prescribed dosage and strengths of Upadacitinib are available in the market?
• What are the common adverse reactions or side effects of Upadacitinib?
• What is the product type, route of administration and mechanism of action of Upadacitinib?
• What are the chemical specifications of Upadacitinib?
• How are the clinical trials diversified on the basis of the trial status?
• What is the history of Upadacitinib, and what is its future?
• What are the marketed details of Upadacitinib 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 Upadacitinib and when these patents will get expire?
• What are the pros (benefits) and cons (disadvantages) of Upadacitinib?
• In which countries Upadacitinib got approval and when it gets launched?
• What are the clinical trials are currently ongoing for Upadacitinib?
• How the safety and efficacy results determined the approval of Upadacitinib?
• What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Upadacitinib development?
• What are the key designations that have been granted to Upadacitinib?
• What is the historical and forecasted market scenario of Upadacitinib?
• How is the market trend of Upadacitinib 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 Upadacitinib?
• Which are the late-stage emerging therapies under development for the treatment of the indicated condition?

TABLE OF CONTENT:

1. Product Overview
1.1. Indication
1.2. Mechanism of Action
1.3. Dosage and Administration
1.4.1 Dosage Forms and Strengths
1.4. Route of Synthesis
1.5. Pharmacology
1.4.2 Pharmacodynamics
1.4.3 Pharmacokinetics
1.6. Adverse Reactions
1.7. Product Snapshot
1.8. Development Milestones of Upadacitinib
1.9. Marketed Details
1.4.4 United States
1.4.5 Europe
1.4.6 Japan
1.10. Patent Details
2. SWOT Analysis
2.1. Analyst Views
3. Regulatory Milestones
3.1. Approvals
3.2. Research and Development
3.3. Clinical Trials Information
3.4. Safety and Efficacy
3.5. Product Developmental Activities
4. Market Assessment

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