STELARA (Ustekinumab), Drug Insight and Market Forecast – 2032

STELARA (Ustekinumab), Drug Insight and Market Forecast – 2032

“STELARA (Ustekinumab), Drug Insight and Market Forecast – 2032” report provides comprehensive insights about STELARA (Ustekinumab) for Crohn’s disease (CD) in the 7MM. A detailed picture of the STELARA (Ustekinumab) for Crohn’s disease (CD) in the 7MM, i.e., United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan, for the study period 2019–2032 is provided in this report along with a detailed description of the STELARA (Ustekinumab) for Crohn’s disease (CD). The report provides insight about mechanism of action, dosage and administration, as well as research and development activity including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the STELARA (Ustekinumab) market forecast, analysis for Crohn’s disease (CD) in the 7MM, descriptive analysis such as SWOT, analyst views, comprehensive overview of market competitors, and brief about other emerging therapies in Crohn’s disease (CD).

Drug Summary

STELARA (Ustekinumab) is a prescription medicine approved for the treatment of adults 18 years and older with moderately to severely active Crohn’s disease and Ulcerative Colitis. There are many different naturally occurring proteins in the body that contribute to inflammation. Patients with Crohn's disease and Ulcerative Colitis are found to have elevated levels of two of these proteins, IL-12 and IL-23. STELARA is the FDA-approved medicine that targets IL-12 and IL-23, which are thought to be associated with gastrointestinal inflammation in Crohn's disease and Ulcerative Colitis.

STELARA is a human IgG1κ monoclonal antibody, is a human interleukin-12 and -23 antagonist. Using DNA recombinant technology, ustekinumab is produced in a murine cell line (Sp2/0). The manufacturing process contains steps for the clearance of viruses. Ustekinumab is comprised of 1326 amino acids and has an estimated molecular mass that ranges from 148,079 to 149,690 Daltons.

Mechanism of Action

Ustekinumab is a human IgG1қ monoclonal antibody that binds with specificity to the p40 protein subunit used by both the IL-12 and IL-23 cytokines. IL-12 and IL-23 are naturally occurring cytokines that are involved in inflammatory and immune responses, such as natural killer cell activation and CD4+ T-cell differentiation and activation. In in vitro models, ustekinumab was shown to disrupt IL-12 and IL-23 mediated signaling and cytokine cascades by disrupting the interaction of these cytokines with a shared cell-surface receptor chain, IL-12Rβ1.

The cytokines IL-12 and IL-23 have been implicated as important contributors to the chronic inflammation that is a hallmark of Crohn’s disease and ulcerative colitis. In animal models of colitis, genetic absence or antibody blockade of the p40 subunit of IL-12 and IL-23, the target of ustekinumab, was shown to be protective.

Scope of the Report

The report provides insights into:

A comprehensive product overview including the STELARA (Ustekinumab) description, mechanism of action, dosage and administration, research and development activities in Crohn’s disease (CD).

Elaborated details on STELARA (Ustekinumab) regulatory milestones and other development activities have been provided in this report.

The report also highlights the STELARA (Ustekinumab) research and development activity in Crohn’s disease (CD) in detail across the United States, Europe and Japan.

The report also covers the patents information with expiry timeline around STELARA (Ustekinumab).

The report contains forecasted sales of STELARA (Ustekinumab) for Crohn’s disease (CD) till 2032.

Comprehensive coverage of the late-stage emerging therapies for Crohn’s disease (CD).

The report also features the SWOT analysis with analyst views for STELARA (Ustekinumab) in Crohn’s disease (CD).

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.

STELARA (Ustekinumab) Analytical Perspective by DelveInsight

In-depth STELARA (Ustekinumab) Market Assessment

This report provides a detailed market assessment of STELARA (Ustekinumab) in Crohn’s disease (CD) in the 7MM, 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 2022 to 2032.

STELARA (Ustekinumab) Clinical Assessment

The report provides the clinical trials information of STELARA (Ustekinumab) in Crohn’s disease (CD) covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

In the coming years, the market scenario for Crohn’s disease (CD) 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 STELARA (Ustekinumab) dominance.

Other emerging products for Crohn’s disease (CD) are expected to give tough market competition to STELARA (Ustekinumab) 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 STELARA (Ustekinumab) in Crohn’s disease (CD).

Our in-depth analysis of the forecasted sales data of STELARA (Ustekinumab) from 2022 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the STELARA (Ustekinumab) in Crohn’s disease (CD).

Key Questions

What is the product type, route of administration and mechanism of action of STELARA (Ustekinumab)?

What is the clinical trial status of the study related to STELARA (Ustekinumab) in Crohn’s disease (CD) and study completion date?

What are the key collaborations, mergers and acquisitions, licensing and other activities related to the STELARA (Ustekinumab) development?

What are the key designations that have been granted to STELARA (Ustekinumab) for Crohn’s disease (CD)?

What is the forecasted market scenario of STELARA (Ustekinumab) for Crohn’s disease (CD)?

What are the forecasted sales of STELARA (Ustekinumab) 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 in Crohn’s disease (CD) and how are they giving competition to STELARA (Ustekinumab) for Crohn’s disease (CD)?

Which are the late-stage emerging therapies under development for the treatment of Crohn’s disease (CD)?