Sung-Soo Park
Proteasome Inhibitor(Sung-Soo Park)은 FRα 표적 세포·유전자 치료로, Multiple Myeloma, Relapsed; Multiple Myeloma (MM) 영역에서 개발·상용화 중입니다. 작용기전: in myofibroblasts remain undefined. 전임상 단계입니다. 대표 임상 효능: ORR 88% (ClinicalTrials.gov NCT01217957). PK: t½ 5 h. 차별점: unique SNPs with significant association with BIPN.
FRα
Multiple Myeloma, Relapsed; Multiple Myeloma (MM)
Recruiting
bispecific antibodies
SN-38-A2 , demonstrates potent TOP1 degradati
linker optimization, CPP-13, a pomalidomide-based degrader with a 13-atom linker, was
unique SNPs with significant association with BIPN
in myofibroblasts remain undefined
macrophage activation
DNA damage, cell cycle distribution, and apoptosis were analysed using immunofluorescence and flow cytometry
resistance to common clinical anti-AML drugs
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Sung-Soo Park
Proteasome Inhibitor(Sung-Soo Park)은 FRα 표적 세포·유전자 치료로, Multiple Myeloma, Relapsed; Multiple Myeloma (MM) 영역에서 개발·상용화 중입니다. 작용기전: in myofibroblasts remain undefined. 전임상 단계입니다. 대표 임상 효능: ORR 88% (ClinicalTrials.gov NCT01217957). PK: t½ 5 h. 차별점: unique SNPs with significant association with BIPN.
FRα
Multiple Myeloma, Relapsed; Multiple Myeloma (MM)
Recruiting
bispecific antibodies
SN-38-A2 , demonstrates potent TOP1 degradati
linker optimization, CPP-13, a pomalidomide-based degrader with a 13-atom linker, was
unique SNPs with significant association with BIPN
in myofibroblasts remain undefined
macrophage activation
DNA damage, cell cycle distribution, and apoptosis were analysed using immunofluorescence and flow cytometry
resistance to common clinical anti-AML drugs
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.