Ado-trastuzumab (T) emtansine (T-DM1)(Roche / Genentech)은 HER2 표적 ADC로, Salivary Gland Cancer; HER2 Gene Mutation 영역에서 개발·상용화 중입니다. 작용기전: targeting human epidermal growth factor receptor. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 74.1% (ClinicalTrials.gov NCT03523585). PK: t½ 4 h. 차별점: novel [ 225 Ac]Ac-labeled pertuzumab-PEGylated emtansine drug conjugate against HER2-positive breast cancer.
HER2
Salivary Gland Cancer; HER2 Gene Mutation
Recruiting
ADCs) are constrained by limited tumor penetration of IgG forma
DM1 via butelase-1 with ABD fusion for pote
linker design, and payload selection
novel [ 225 Ac]Ac-labeled pertuzumab-PEGylated emtansine drug conjugate against HER2-positive breast cancer
targeting human epidermal growth factor receptor
NK cell cytotoxicity
payload selection
HER2-positive
Bypass the Binding-Site Barrier
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Ado-trastuzumab (T) emtansine (T-DM1)(Roche / Genentech)은 HER2 표적 ADC로, Salivary Gland Cancer; HER2 Gene Mutation 영역에서 개발·상용화 중입니다. 작용기전: targeting human epidermal growth factor receptor. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 74.1% (ClinicalTrials.gov NCT03523585). PK: t½ 4 h. 차별점: novel [ 225 Ac]Ac-labeled pertuzumab-PEGylated emtansine drug conjugate against HER2-positive breast cancer.
HER2
Salivary Gland Cancer; HER2 Gene Mutation
Recruiting
ADCs) are constrained by limited tumor penetration of IgG forma
DM1 via butelase-1 with ABD fusion for pote
linker design, and payload selection
novel [ 225 Ac]Ac-labeled pertuzumab-PEGylated emtansine drug conjugate against HER2-positive breast cancer
targeting human epidermal growth factor receptor
NK cell cytotoxicity
payload selection
HER2-positive
Bypass the Binding-Site Barrier
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.