Sunitinib Malate(Pfizer)은 FRα 표적 ADC로, Advanced Lymphoma; Advanced Malignant Solid Neoplasm 영역에서 개발·상용화 중입니다. 작용기전: targeted tyrosine kinase inhibitor that inhibits tumor angiogenesis and proliferation by blocking signaling. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 59% (ClinicalTrials.gov NCT03729245). 차별점: Novel 1-benzyl-2-indolinone indole hybrids as tyrosine kinase inhibitors: Design, synthesis, and biological activity evaluati.
FRα
Advanced Lymphoma; Advanced Malignant Solid Neoplasm
Recruiting
Novel 1-benzyl-2-indolinone indole hybrids as tyrosine kinase inhibitors: Design, synthesis, and biological activity evaluati
targeted tyrosine kinase inhibitor that inhibits tumor angiogenesis and proliferation by blocking signaling
apoptosis, accompanied by reduced ERK signalings
biomarker
downregulation of c-MYC, TWIST, and MMP2 expression both in vitro and in vivo following sunitinib malate treatment
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Sunitinib Malate(Pfizer)은 FRα 표적 ADC로, Advanced Lymphoma; Advanced Malignant Solid Neoplasm 영역에서 개발·상용화 중입니다. 작용기전: targeted tyrosine kinase inhibitor that inhibits tumor angiogenesis and proliferation by blocking signaling. Phase 2에서 효능·안전성 신호를 검증 중입니다. 대표 임상 효능: ORR 59% (ClinicalTrials.gov NCT03729245). 차별점: Novel 1-benzyl-2-indolinone indole hybrids as tyrosine kinase inhibitors: Design, synthesis, and biological activity evaluati.
FRα
Advanced Lymphoma; Advanced Malignant Solid Neoplasm
Recruiting
Novel 1-benzyl-2-indolinone indole hybrids as tyrosine kinase inhibitors: Design, synthesis, and biological activity evaluati
targeted tyrosine kinase inhibitor that inhibits tumor angiogenesis and proliferation by blocking signaling
apoptosis, accompanied by reduced ERK signalings
biomarker
downregulation of c-MYC, TWIST, and MMP2 expression both in vitro and in vivo following sunitinib malate treatment
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.