Seagen Inc.
SGN-35(Seagen Inc.)은 Disease, Hodgkin 표적 ADC로, Disease, Hodgkin; Lymphoma, Large-Cell, Anaplastic 영역에서 개발·상용화 중입니다. 작용기전: ADC pinocytosis-dependent for T-DM1. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 89.5% (ClinicalTrials.gov NCT02588651). 차별점: novel Teliso-V PBPK-model.
Disease, Hodgkin
Disease, Hodgkin; Lymphoma, Large-Cell, Anaplastic
Active
ADCs) are complex drug platforms composed of monoclonal antibod
Vedotin for Relapsed or Refractory Sézary
linkers, enabling selective payload delivery to neoplastic cells, resulting in improve
novel Teliso-V PBPK-model
ADC pinocytosis-dependent for T-DM1
T-cell lymphoma via spindle assembly checkpoint activation
microtubule-disrupting agent monomethylauristatin E
biomarker-driven clinical trials
resistance mechanisms remain poorly understood
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Seagen Inc.
SGN-35(Seagen Inc.)은 Disease, Hodgkin 표적 ADC로, Disease, Hodgkin; Lymphoma, Large-Cell, Anaplastic 영역에서 개발·상용화 중입니다. 작용기전: ADC pinocytosis-dependent for T-DM1. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 89.5% (ClinicalTrials.gov NCT02588651). 차별점: novel Teliso-V PBPK-model.
Disease, Hodgkin
Disease, Hodgkin; Lymphoma, Large-Cell, Anaplastic
Active
ADCs) are complex drug platforms composed of monoclonal antibod
Vedotin for Relapsed or Refractory Sézary
linkers, enabling selective payload delivery to neoplastic cells, resulting in improve
novel Teliso-V PBPK-model
ADC pinocytosis-dependent for T-DM1
T-cell lymphoma via spindle assembly checkpoint activation
microtubule-disrupting agent monomethylauristatin E
biomarker-driven clinical trials
resistance mechanisms remain poorly understood
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.