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HMBD-001 Market Size, Forecast, and Emerging Insight – 2032

Published Date : 2023
Pages : 30
Region : United States, Japan, EU4 & UK
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HMBD-001 Emerging Drug Insight

“HMBD-001 Market Size, Forecast, and Emerging Insight – 2032” report provides comprehensive insights about HMBD-001 for Rare NRG1 Fusion in the seven major markets. A detailed picture of the HMBD-001 for Rare NRG1 Fusion  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 HMBD-001 for Rare NRG1 Fusion .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 HMBD-001 market forecast, analysis for Rare NRG1 Fusion in the 7MM descriptive analysis such as SWOT, analyst views, comprehensive overview of market competitors, and brief about other emerging therapies in Rare NRG1 Fusion.

Drug Summary

HMBD-001 is a unique antibody engineered to bind strongly and specifically to the dimerization interface of HER3, thereby interfering with HER3’s ability to dimerize and fully blocking its activation, regardless of NRG1 binding. This gives HMBD-001 a novel action mechanism for inhibiting tumor growth and drug resistance in HER3-driven cancers. Preclinical models have shown that HMBD-001 potently inhibits the activation of the MAPK/PI3K signaling pathway – and consequently prevents tumor growth and drug resistance.

 

HMBD-001 has broad potential across multiple tumor types; however, optimal clinical development requires a “stepping-stone” strategy to demonstrate benefit and ensure efficient deployment of resources. Through integrative AI-powered analyses of robust datasets, the company has identified biomarkers indicative of certain patient populations who may benefit most from HMBD-001, for example, patients with functional NRG1 fusions in their tumors.

 

The company aims to evaluate HMBD-001 for the treatment of patients with cancers expressing NRG1 fusions, as well as other priority patient populations for precision oncology, with their partner, Cancer Research UK (CRUK).

 

In December 2021, the first patient was dosed in the Phase I clinical trial of HMBD-001 for the treatment of patients with advanced HER3-expressing solid malignancies (NCT05057013).

 

The Phase I clinical trial in the United Kingdom is being sponsored and managed by Cancer Research UK’s Centre for Drug Development and led by Chief Investigator, Professor Johann De Bono at the Royal Marsden Hospital and The Institute of Cancer Research, London. The trial intends to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics and explore preliminary evidence of HMBD-001 activity in patients with advanced HER3-expressing solid malignancies, including NRG1 fusion-driven cancers.

Scope of the Report

The report provides insights into:

  • A comprehensive product overview including the HMBD-001 description, mechanism of action, dosage and administration, research and development activities in Rare NRG1 Fusion.
  • Elaborated details on HMBD-001 regulatory milestones and other development activities have been provided in this report.
  • The report also highlights the HMBD-001 research and development activity in Rare NRG1 Fusion in detail across the United States, Europe and Japan.
  • The report also covers the patents information with expiry timeline around HMBD-001.
  • The report contains forecasted sales of HMBD-001 for Rare NRG1 Fusion till 2032.
  • Comprehensive coverage of the late-stage emerging therapies for Rare NRG1 Fusion.
  • The report also features the SWOT analysis with analyst views for HMBD-001 in Rare NRG1 Fusion.

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.

HMBD-001 Analytical Perspective by DelveInsight

In-depth HMBD-001 Market Assessment

This report provides a detailed market assessment of HMBD-001 in Rare NRG1 Fusion 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 2027 to 2032.

 

HMBD-001 Clinical Assessment

The report provides the clinical trials information of HMBD-001 in Rare NRG1 Fusion covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights 

  • In the coming years, the market scenario for Rare NRG1 Fusion 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 HMBD-001 dominance.
  • Other emerging products for Rare NRG1 Fusion are expected to give tough market competition to HMBD-001 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 HMBD-001 in Rare NRG1 Fusion.
  • Our in-depth analysis of the forecasted sales data from 2027 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the HMBD-001 in Rare NRG1 Fusion.

Key Questions

  • What is the product type, route of administration and mechanism of action of HMBD-001?
  • What is the clinical trial status of the study related to HMBD-001 in Rare NRG1 Fusion and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the HMBD-001 development?
  • What are the key designations that have been granted to HMBD-001 for Rare NRG1 Fusion?
  • What is the forecasted market scenario of HMBD-001 for Rare NRG1 Fusion?
  • What are the forecasted sales of HMBD-001 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 Rare NRG1 Fusion and how are they giving competition to HMBD-001 for Rare NRG1 Fusion?
  • Which are the late-stage emerging therapies under development for the treatment of Rare NRG1 Fusion?

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