EO2401-1 Emerging Drug Insight

“EO2401-1 Market Size, Forecast, and Emerging Insight – 2032” report provides comprehensive insights about EO2401-1 for Glioblastoma Multiforme (GBM) in the seven major markets. A detailed picture of the EO2401-1 for GBM 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 EO2401-1 for GBM. 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 EO2401-1 market forecast analysis for GBM in the 7MM, SWOT, analysts’ views, comprehensive overview of market competitors, and brief about other emerging therapies in GBM.

Drug Summary

A donor-derived, off-the-shelf, microbiome therapeutic cancer peptide vaccine composed of three bacterial Oncomimics, immunogenic microbiome-derived peptides that are highly homologous to tumor-associated antigens (TAAs), that are obtained and selected from the human gut microbiome and are specific for brain tumors, including GBM, with potential immunomodulating and antineoplastic activities. The three microbiome-derived bacterial antigens in EO2401 mimic three TAAs that are highly expressed by brain tumors. Upon administration of microbiome-derived peptide vaccine EO2401, the peptides are taken up and presented on dendritic cells (DCs) to T cells. As the presented antigens display molecular mimicry with selected TAAs on brain cancer cells, a memory T-cell- and cytotoxic T-lymphocyte (CTL)-mediated immune response may be mounted against the TAAs expressed on the brain cancer cells, thereby eradicating the brain cancer cells. EO2401 in combination with an immune checkpoint inhibitor (nivolumab, OPDIVO) ± bevacizumab for treating patients with first progression/recurrence of GBM. EO2401 is Enterome’s first-in-class off-the-shelf OncoMimics cancer immunotherapy. It combines three OncoMimics peptides that closely mimic IL13Ra2, BIRC5, and FOXM1, all known driver antigens on aggressive solid tumors. In addition, EO2401 contains a CD4 helper peptide UCP2. Enterome selected these OncoMimics peptides using its Mimicry platform, which applies best-in-class biocomputational tools and bioassays to identify novel therapeutics from its proprietary database of 20+ million bioactive gut microbiome peptides and proteins. The study aims to assess the safety, tolerability, immunogenicity, and preliminary efficacy of the combination in approximately 100 patients enrolled at 10 clinical sites in Europe and the US (Enterome, 2022). As per the company, the pivotal trial for GBM is partnered with Bristol Myers Squibb.

In 2022, the company announced that new data from its two Phase I/II clinical trials of EO2401 in combination with nivolumab (OPDIVO) ± bevacizumab (AVASTIN) in patients with first progression/rGBM (ROSALIE trial), and combination with nivolumab in patients with non-resectable adrenocortical carcinomas (ACC) and metastatic pheochromocytoma/paraganglioma (MPP) (SPENCER trial).

Scope of the Report

The report provides insights into:

A comprehensive product overview including the EO2401-1 description, mechanism of action, dosage and administration, research and development activities in GBM.

Elaborated details on EO2401-1 regulatory milestones and other development activities have been provided in this report.

The report also highlights the EO2401-1 research and development activities in GBM across the United States, Europe and Japan.

The report also covers the patents information with expiry timeline around EO2401-1.

The report contains forecasted sales of for GBM till 2032.

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

The report also features the SWOT analysis with analyst views for EO2401-1 in GBM.

 

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.

 

EO2401-1 Analytical Perspective by DelveInsight

In-depth EO2401-1 Market Assessment

This report provides a detailed market assessment of EO2401-1 for GBM 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 of EO2401-1.

 

EO2401-1 Clinical Assessment

The report provides the clinical trials information of EO2401-1 for GBM covering trial interventions, trial conditions, trial status, start and completion dates.

 

Report Highlights 

In the coming years, the market scenario for GBM 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 EO2401-1 dominance.

Other emerging products for GBM are expected to give tough market competition to EO2401-1 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 EO2401-1 in GBM.

Our in-depth analysis of the forecasted sales data of EO2401-1 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the EO2401-1 in GBM.

 

Key Questions

What is the product type, route of administration and mechanism of action of EO2401-1?

What is the clinical trial status of the study related to EO2401-1 in GBM and study completion date?

What are the key collaborations, mergers and acquisitions, licensing and other activities related to the EO2401-1 development?

What are the key designations that have been granted to EO2401-1 for GBM?

What is the forecasted market scenario of EO2401-1 for GBM?

What are the forecasted sales of EO2401-1 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 EO2401-1 for GBM?

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