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시장보고서
상품코드
1462287
CSL112 시장 규모, 예측, 신약 인사이트(2032년)CSL112 Market Size, Forecast, and Emerging Insight - 2032 |
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CSL112(Apolipoprotein A-I(human))는 HDL의 주요 기능 성분인 혈장 유래 ApoA-I의 새로운 제제입니다. CSL112는 정맥 투여에 적합한 HDL 유사 입자로 재구성되며, 연구에 따르면 CSL112를 정맥주사하면 콜레스테롤 배출 능력이 빠르게 향상되고, 동맥경화성 플라크 병변을 빠르게 안정화시키는 새로운 접근법을 제공할 수 있으며, 급성 심근경색 급성 심근경색 환자의 조기 심혈관계 질환의 위험을 줄이기 위해 개발되고 있습니다.
기업의 R&D 투자자 설명회에 따르면 3상 임상시험(AEGIS-II) 모집은 2022년 12월 LPI를 향해 순조롭게 진행되고 있습니다. 시험은 진행 중이며, 80% 이상의 등록을 달성했고, 세 번째 중간 분석이 완료되었습니다. 임상은 2023년까지 완료될 예정이며, 출시는 2025년 4분기로 예정되어 있습니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 심근경색용 CSL112에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"CSL112 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about CSL112 for myocardial infarction in the seven major markets. A detailed picture of the CSL112 for myocardial infarction 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 CSL112 for myocardial infarction. 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 CSL112 market forecast analysis for myocardial infarction in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in myocardial infarction.
CSL112, apolipoprotein A-I (human), is a novel formulation of plasma-derived apoA-I, the primary functional component of HDL. It is reconstituted to form HDL-like particles suitable for IV infusion. Studies have shown that infusion of CSL112 rapidly enhances cholesterol efflux capacity. CSL112 may offer a new approach for rapidly stabilizing atherosclerotic plaque lesions and is being developed to reduce the risk of early cardiovascular events in acute MI patients.
As per the company's R&D investor briefing presentation, recruitment of the Phase III study (AEGIS-II) is on track for LPI December 2022. The study is progressing with >80% enrolment achieved and the third interim analysis completed. The trial is expected to be completed by 2023, and the launch is expected for Q4 of 2025.
The report provides insights into:
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.
CSL112 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of CSL112 for myocardial infarction 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 CSL112 for myocardial infarction covering trial interventions, trial conditions, trial status, start and completion dates.