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시장보고서
상품코드
1462283
ASC22 시장 규모, 예측, 신약 인사이트(2032년)ASC22 Market Size, Forecast, and Emerging Insight - 2032 |
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envafolimab으로도 알려진 ASC22는 만성 B형 간염(CHB)의 기능적 치료를 목표로 하는 최초의 피하 투여형 PD-L1 항체입니다. 이 항체는 피하 주사가 가능하고 상온에서 안정성이 높다는 장점이 있으며, Ascletis Pharma는 ASC22의 바이러스성 적응증에 대한 전 세계 독점 개발권 및 상업화 권리를 보유하고 있습니다.
현재 이 약은 CHB 치료에서 ASC22의 단회 및 다회 투여 후 안전성과 유효성을 평가하기 위한 임상 II상 시험(NCT04465890)을 진행 중입니다. 중국 임상 IIb상 중간 결과에 따르면 24주 동안 1mg/kg의 ASC22와 NA를 24주간 투여한 결과, CHB 환자에서 양호한 내약성을 보였습니다. 기준치 HBsAg가 100IU/mL 미만인 환자의 42.9%가 지속적인 HBsAg 소실을 보였으며, 이는 기능적 치료 가능성을 시사합니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 B형 만성 간염(CHB)용 ASC22에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"ASC22 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about ASC22 for chronic hepatitis B in the seven major markets and China. A detailed picture of the ASC22 for chronic hepatitis B in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Japan, and China for the study period 2019 -2032 is provided in this report along with a detailed description of the ASC22 for chronic hepatitis B. 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 ASC22 market forecast analysis for chronic hepatitis B in the 7MM and China, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in chronic hepatitis B.
ASC22, also known as envafolimab, is a first-in-class, subcutaneously administered PD-L1 antibody for chronic hepatitis B (CHB) functional cure. It has the advantages of SC injection and good stability at room temperature. These would be of great value to improve patient's compliance and quality of life and to help realize the goal of long-term management of chronic diseases such as chronic hepatitis B. Ascletis Pharma retains the global and exclusive rights to develop and commercialize ASC22 on viral indications.
Currently, the drug is being evaluated in a Phase II (NCT04465890) trial to evaluate the safety and efficacy of ASC22 in treating CHB after single and multiple drug administration. Interim results from the China Phase IIb clinical trial showed 1 mg/kg of ASC22 plus NAs for 24-week treatment were well-tolerated in CHB patients. 42.9% of patients with baseline HBsAg <=100 IU/mL obtained sustained HBsAg loss, which indicates the potential of functional cure.
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.
ASC22 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of ASC22 for chronic hepatitis B in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, Japan, and China. This segment of the report provides forecasted sales data from 2027 to 2032.
The report provides the clinical trials information of ASC22 for chronic hepatitis B covering trial interventions, trial conditions, trial status, start and completion dates.