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시장보고서
상품코드
1462274
VRDN-001 시장 규모, 예측, 신약 인사이트(2032년)VRDN-001 Market Size, Forecast, and Emerging Insight - 2032 |
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Viridian의 주요 제품 후보물질인 VRDN-001은 인슐린 유사 성장인자 1 수용체(IGF-1R)를 표적으로 하는 분화 단클론 항체로서, 임상 및 상업적 검증을 거쳐 베체트병 안질환 치료제로 개발되고 있습니다.
전 임상시험에서 VRDN-001은 IGF-1R의 완전한 길항제로서 유일하게 승인된 다른 항 IGF-1R 항체를 포함한 다른 항-IGF-1R 항체보다 더 완벽하게 수용체를 차단하는 것으로 나타났습니다. 현재 진행 중인 임상 2상 시험의 첫 번째 투여 코호트에서 얻은 데이터는 활동성 그레이브스병 안질환 환자에서 VRDN-001의 임상적 개념 증명을 확립했습니다. 현재 진행 중인 임상시험의 예비 데이터에 따르면 VRDN-001은 임상적으로 유의미한 전안부 증상 감소, 임상적 활동성 점수(CAS) 개선, 복시 소실 등의 효과를 보였으며, VRDN-001은 임상시험에서 전반적으로 안전하고 내약성이 양호한 것으로 나타났습니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 그레이브스 안병증용 VRDN-001에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"VRDN-001 Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about VRDN-001 for Graves' Ophthalmopathy in the seven major markets. A detailed picture of the VRDN-001 for Graves' Ophthalmopathy 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 VRDN-001 for Graves' Ophthalmopathy. 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 VRDN-001 market forecast analysis for Graves' Ophthalmopathy in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Graves' Ophthalmopathy.
Viridian's lead product candidate, VRDN-001, is a differentiated monoclonal antibody targeting insulin-like growth factor-1 receptor (IGF-1R), a clinically and commercially validated target for the treatment of Graves' Ophthalmopathy.
In preclinical studies, VRDN-001 had shown to be a full antagonist of IGF-1R, with complete receptor blockade than other anti-IGF-1R antibodies, including the only approved Graves' Ophthalmopathy therapy. Data from the initial dose cohorts of the Phase II portion of the ongoing trial established clinical proof-of-concept for VRDN-001 in patients with active Graves' Ophthalmopathy. Preliminary data from the ongoing trial showed treatment with VRDN-001 led to clinically meaningful reductions in proptosis, improvement in clinical activity score (CAS), and diplopia resolution. VRDN-001 was generally safe and well-tolerated in the trial.
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.
VRDN-001 Analytical Perspective by DelveInsight
This report provides a detailed market assessment of VRDN-001 for Graves' Ophthalmopathy 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 VRDN-001 for Graves' Ophthalmopathy covering trial interventions, trial conditions, trial status, start and completion dates.