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시장보고서
상품코드
1462307
OPDIVO 시장 규모, 예측, 신약 인사이트(2032년)OPDIVO Market Size, Forecast, and Emerging Insight - 2032 |
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OPDIVO(Opdivo, 니볼루맙)는 인간 최초의 면역글로불린 G4(IgG4) PD-1 면역 체크포인트 억제 항체로서 PD-1 수용체와 그 리간드인 PD-L1과 PD-L2의 상호 작용을 억제하여 세포성 면역반응을 억제합니다. 표적 면역치료는 현재 종양 환자들에게 가장 유망한 치료법으로 떠오르고 있습니다. 활성화된 T세포에 발현된 PD-1은 면역 억제를 역전시켜 T세포의 활성화를 해제할 수 있습니다. 니볼루맙은 이미 확립된 약물로, 현재 다양한 적응증과 다양한 환자군에 대한 승인을 받았습니다.
현재 재발성 상피성 난소암을 대상으로 한 임상 2상 시험(NCT02873962)을 통해 이 약물을 평가했습니다.
주요 6 시장(미국·독일·프랑스·이탈리아·스페인·영국)에서 난소암용 OPDIVO에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"OPDIVO Market Size, Forecast, and Emerging Insight - 2032" report provides comprehensive insights about OPDIVO for ovarian cancer in the six major markets. A detailed picture of the OPDIVO for ovarian cancer in the 6MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom for the study period 2019 -2032 is provided in this report along with a detailed description of the OPDIVO for ovarian cancer. 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 OPDIVO market forecast analysis for ovarian cancer in the 6MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in ovarian cancer.
OPDIVO (also known as Nivolumab) is the first-in-human immunoglobulin G4 (IgG4) PD-1 immune checkpoint inhibitor antibody that disrupts the interaction of the PD-1 receptor with its ligands PD-L1 and PD-L2, thereby inhibiting the cellular immune response. Targeted immunotherapy has now become the most promising approach for tumor patients. PD-1 expressed on activated T-cells can reverse immune suppression and release T-cell activation. Nivolumab is an already established drug and is currently approved in different indications and for different patient segments.
Currently, the drug is being developed in a Phase II (NCT02873962) clinical study evaluating the drug in relapsed epithelial ovarian cancer.
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.
OPDIVO Analytical Perspective by DelveInsight
This report provides a detailed market assessment of OPDIVO for ovarian cancer in the six major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom. This segment of the report provides forecasted sales data from 2026 to 2032.
The report provides the clinical trials information of OPDIVO for ovarian cancer covering trial interventions, trial conditions, trial status, start and completion dates.