DUBLIN–(BUSINESS WIRE)–The “US HUMIRA Market Size, Forecast, and Market Insight – 2032” report has been added to ResearchAndMarkets.com’s offering.
This report provides comprehensive insights about HUMIRA for autoimmune uveitis in the US. A detailed picture of the HUMIRA for autoimmune uveitis in the US for the study period 2019 -2032 is provided in this report along with a detailed description of the HUMIRA for autoimmune uveitis.
The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the HUMIRA market forecast analysis for autoimmune uveitis in the US, SWOT, analysts’ views, comprehensive overview of market competitors, and brief about other emerging therapies in autoimmune uveitis.
Drug Summary
HUMIRA is the commercially available preparation of adalimumab being developed by AbbVie Inc. for treating noninfectious intermediate, posterior, and panuveitis; it acts by binding to the tumor necrosis factor (TNF) alpha. Thus, it inhibits TNF-mediated immune responses by preventing its binding to p55 and p75 cell surface TNF receptors. It limits the autoimmune response by preventing the induction of inflammatory cytokines, thus limiting autoimmune response.
It is approved for the treatment of rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis (PsA), ankylosing spondylitis (AS), hidradenitis suppurativa (HS), adult Crohn’s disease (CD), pediatric Crohn’s disease, plaque psoriasis and ulcerative colitis (UC). It is approved in the United States, Europe, and Japan for treating noninfectious intermediate, posterior, and panuveitis. This is the 10th approved indication of HUMIRA in the US, followed by European approval.
Scope of the Report
The report provides insights into:
- A comprehensive product overview including the HUMIRA description, mechanism of action, dosage and administration, research and development activities in autoimmune uveitis.
- Elaborated details on HUMIRA regulatory milestones and other development activities have been provided in this report.
- The report also highlights the HUMIRA research and development activities in autoimmune uveitis across the US.
- The report also covers the patents information with expiry timeline around HUMIRA.
- The report contains forecasted sales of HUMIRA for autoimmune uveitis till 2032.
- Comprehensive coverage of the late-stage emerging therapies for autoimmune uveitis.
- The report also features the SWOT analysis with analyst views for HUMIRA in autoimmune uveitis.
HUMIRA Analytical Perspective
In-depth HUMIRA Market Assessment
This report provides a detailed market assessment of HUMIRA for autoimmune uveitis in the US. This segment of the report provides forecasted sales data from 2024 to 2032.
HUMIRA Clinical Assessment
The report provides the clinical trials information of HUMIRA for autoimmune uveitis covering trial interventions, trial conditions, trial status, start and completion dates.
Report Highlights
- In the coming years, the market scenario for autoimmune uveitis 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 are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence HUMIRA dominance.
- Other emerging products for autoimmune uveitis are expected to give tough market competition to HUMIRA and launch of late-stage emerging therapies in the near future will significantly impact the market.
- A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of HUMIRA in autoimmune uveitis.
- In-depth analysis of the forecasted sales data of HUMIRA from 2024 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the HUMIRA in autoimmune uveitis.
Key Questions Answered
- What is the product type, route of administration and mechanism of action of HUMIRA?
- What is the clinical trial status of the study related to HUMIRA in autoimmune uveitis and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the HUMIRA development?
- What are the key designations that have been granted to HUMIRA for autoimmune uveitis?
- What is the forecasted market scenario of HUMIRA for autoimmune uveitis?
- What are the forecasted sales of HUMIRA in the US?
- What are the other emerging products available and how are these giving competition to HUMIRA for autoimmune uveitis?
- Which are the late-stage emerging therapies under development for the treatment of autoimmune uveitis?
Key Topics Covered:
1. Report Introduction
2. HUMIRA Overview in autoimmune uveitis
2.1. Product Detail
2.2. Clinical Development
2.2.1. Clinical studies
2.2.2. Clinical trials information
2.2.3. Safety and efficacy
2.3. Regulatory Milestones
2.4. Other Developmental Activities
2.5. Product Profile
3. Competitive Landscape (Marketed Therapies)
4. Competitive Landscape (Late-stage Emerging Therapies)
5. HUMIRA Market Assessment
5.1. Market Outlook of HUMIRA in autoimmune uveitis
5.2. The US Analysis
5.2.1. Market Size of HUMIRA in the US for autoimmune uveitis
6. SWOT Analysis
7. Analysts’ Views
8. Appendix
For more information about this report visit https://www.researchandmarkets.com/r/swhvea
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