PUBLISHER: DelveInsight | PRODUCT CODE: 1397522
PUBLISHER: DelveInsight | PRODUCT CODE: 1397522
"Maveropepimut-S Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about maveropepimut-S for Diffuse Large B-cell lymphoma (DLBCL) in the seven major markets. A detailed picture of the maveropepimut-S for DLBCL 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 maveropepimut-S for DLBCL. 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 maveropepimut-S market forecast analysis for DLBCL in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in DLBCL.
Maveropepimut-S (MVP-S), (previously known as DPX-Survivac) is a DPX-based immunotherapy that delivers antigenic peptides of survivin to eliminate survivin-expressing cells by educated, cytotoxic T cells (IMV, 2022a).
Maveropepimut-S is administered with oral intermittent low-dose cyclophosphamide (CPA), which can act as an immune modulator, increasing the number of survivin-specific T cells generated without inducing significant cytotoxicity.
Currently, Maveropepimut-S is being tested in a Phase IIb (VITALIZ) trial in R/R DLBCL. Site activation and enrollment in the VITALIZE Phase IIb clinical trial increased during the third quarter of 2022. VITALIZE is designed to evaluate the clinical benefit of MVP-S in combination with Merck's anti-PD-1 therapy, KEYTRUDA (pembrolizumab), in patients with R/R DLBCL. Details on the VITALIZE Phase IIb study were presented as a trial-in-progress poster at the European Society for Medical Oncology 2022. The company will present clinical response data in a plenary session at the ImmunoOncology 360 (IO360) conference. IMV is on track to complete enrollment in the first study stage by H1 2023.
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.
This report provides a detailed market assessment of maveropepimut-S for Diffuse Large B-cell lymphoma (DLBCL) 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 2025 to 2032.
The report provides the clinical trials information of maveropepimut-S for DLBCL covering trial interventions, trial conditions, trial status, start and completion dates.