DUPIXENT Market Size, Forecast, and Market Insight - 2032

DUPIXENT Market Size, Forecast, and Market Insight − 2032

“DUPIXENT Market Size, Forecast, and Market Insight − 2032” report provides comprehensive insights about DUPIXENT for Asthma in the seven major markets. A detailed picture of the DUPIXENT for Asthma in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and 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 DUPIXENT for Asthma. 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 DUPIXENT market forecast analysis for Asthma in the 7MM, SWOT, analysts’ views, comprehensive overview of market competitors, and brief about other emerging therapies in Asthma.

Drug Summary

DUPIXENT, invented using Regeneron’s proprietary VelocImmune technology, is a fully human monoclonal antibody that inhibits the signaling of the interleukin-4 (IL-4) and interleukin-13 (IL-13) pathways and is not an immunosuppressant.

DUPIXENT is an injection under the skin (SC injection) at different sites. For pediatric patients aged 6–11, DUPIXENT dosing is based on weight (100 mg every 2 weeks or 300 mg every 4 weeks for children ≥15 to <30 kg, and 200 mg every 2 weeks for children ≥30 kg) and is supplied as a prefilled syringe. It is also available as a prefilled pen for adolescents (12–17 years) and adults at 200 mg and 300 mg doses. DUPIXENT is intended for use under the guidance of a healthcare professional and can be given in a clinic or at home by self-administration after training by a healthcare professional. In children younger than 12, DUPIXENT should be administered by a caregiver if given at home.

Scope of the Report

The report provides insights into:

A comprehensive product overview including the DUPIXENT description, mechanism of action, dosage and administration, research and development activities in Asthma.

Elaborated details on DUPIXENT regulatory milestones and other development activities have been provided in this report.

The report also highlights the DUPIXENT research and development activities in Asthma across the United States, Europe, and Japan.

The report also covers the patents information with expiry timeline around DUPIXENT.

The report contains forecasted sales of DUPIXENT for Asthma till 2032.

Comprehensive coverage of the late-stage emerging therapies for Asthma.

The report also features the SWOT analysis with analyst views for DUPIXENT in Asthma.

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.

DUPIXENT Analytical Perspective by DelveInsight

In-depth DUPIXENT Market Assessment

This report provides a detailed market assessment of DUPIXENT for Asthma in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2024 to 2032.

DUPIXENT Clinical Assessment

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

Report Highlights

In the coming years, the market scenario for Asthma 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 DUPIXENT dominance.

Other emerging products for Asthma are expected to give tough market competition to DUPIXENT 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 DUPIXENT in Asthma.

Our in-depth analysis of the forecasted sales data of DUPIXENT from 2024 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the DUPIXENT in Asthma.

Key Questions

What is the product type, route of administration and mechanism of action of DUPIXENT?

What is the clinical trial status of the study related to DUPIXENT in Asthma and study completion date?

What are the key collaborations, mergers and acquisitions, licensing and other activities related to the DUPIXENT development?

What are the key designations that have been granted to DUPIXENT for Asthma?

What is the forecasted market scenario of DUPIXENT for Asthma?

What are the forecasted sales of DUPIXENT 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 are these giving competition to DUPIXENT for Asthma?

Which are the late-stage emerging therapies under development for the treatment of Asthma?