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시장보고서
상품코드
1397391
DB102 신약에 대한 인사이트 및 시장 예측(2032년)DB102 Emerging Drug Insight and Market Forecast - 2032 |
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DB102(Enzastaurin)는 PKCβ, PI3K, AKT 경로를 억제하는 최초의 경구용 저분자 세린-스레오닌 키나아제 억제제이며, Eli Lilly가 개발하고 Denovo가 전 세계 판권을 획득했습니다.
Denovo는 DLBCL 및 GBM 환자에서 기대되는 치료 효과와 유의미한 상관관계가 있는 바이오마커를 확인하여 국제 특허를 출원했으며, 2018년에 매우 중요한 국제 공동 DLBCL 3상 임상시험을 시작했습니다. 스탠포드 대학으로부터 폐동맥 고혈압(PAH)에 대한 DB102의 사용권을 획득했습니다.
현재 바이오마커 DGM1(Denovo Genomic Marker 1)을 가진 신규 진단 고위험군(IPI >=3) DLBCL 환자를 대상으로 DB102와 R-CHOP 병용요법 및 R-CHOP 단독요법의 유효성을 평가하기 위한 임상 3상을 진행 중입니다. 또한, 회사는 2022년까지 이 임상 3상 시험의 탑라인 데이터를 발표할 예정입니다. 그러나 현재로서는 이에 대한 최신 정보가 없습니다.
이 보고서는 주요 7개국 DB102 시장에 대해 조사했으며, 시장 개요와 함께 2024-2032년까지의 매출 예측 데이터, 경쟁 상황, 국가별 동향 등의 정보를 전해드립니다.
"DB102 Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about DB102 for Diffuse Large B-cell lymphoma (DLBCL) in the seven major markets. A detailed picture of the DB102 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 DB102 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 DB102 market forecast analysis for DLBCL in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in DLBCL.
DB102 (Enzastaurin) is an orally available investigational first-in-class small molecule, serine/threonine kinase inhibitor of the PKC beta, PI3K, and AKT pathways that have been studied in more than 3,000 patients across a range of solid and hematological tumor types. Eli Lilly originally developed DB102 and for which Denovo has acquired worldwide rights.
Denovo has completed the biomarker identification, significantly correlated with the expected therapeutic effects on DLBCL and GBM patients, and has filed international patent applications. Denovo initiated a pivotal Phase III global DLBCL clinical trial in 2018. In 2018, Denovo licensed the rights to use DB102 for pulmonary arterial hypertension (PAH) from Stanford University.
Currently, the drug is in a Phase III trial evaluating the efficacy of DB102 in combination with R-CHOP vs. R-CHOP alone in newly diagnosed high-risk (IPI >=3) DLBCL patients with the biomarker DGM1 (Denovo Genomic Marker 1) (Denovo Biopharma, 2021a). Moreover, the company has also anticipated announcing the topline data of this Phase III trial by 2022. However, so far, there is no update regarding this.
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 DB102 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 2024 to 2032.
The report provides the clinical trials information of DB102 for DLBCL covering trial interventions, trial conditions, trial status, start and completion dates.