Janssen ResearchDevelopmentLLC
Fluorouracil(Janssen Research & Development, LLC)은 Muscle Invasive Bladder Carcinoma 표적 치료제로, Advanced or Metastatic Colorectal Cancer 영역에서 개발·상용화 중입니다. 작용기전: inhibits GC cell proliferation and induces apoptosis by regulating cell-cycle checkpoints and inhibiting oncogenic pathway. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 80% (ClinicalTrials.gov NCT04430738). 차별점: novel ternary copper-deferiprone-phenanthroline complex was rationally designed, synthesized, and thoroughly characterized.
Muscle Invasive Bladder Carcinoma
Advanced or Metastatic Colorectal Cancer
Recruiting
novel ternary copper-deferiprone-phenanthroline complex was rationally designed, synthesized, and thoroughly characterized
inhibits GC cell proliferation and induces apoptosis by regulating cell-cycle checkpoints and inhibiting oncogenic pathway
t cells to oxaliplatin (L-OHP) and 5-fluorouracil (5FU), an effect that was reversible upon PI3K pathway activation
DNA damage, with etoposide exhibiting the highest tail intensity (~60 %)
biomarker for metabolic state, B-cell/TLS-associated immune features, and vulnerability to DNA damage-based t
downregulation of PD-L1 via the IL-6/JAK/STAT3 pathway, reduction of immunosuppression, and promotion of immunogenic cell death (ICD)
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Janssen ResearchDevelopmentLLC
Fluorouracil(Janssen Research & Development, LLC)은 Muscle Invasive Bladder Carcinoma 표적 치료제로, Advanced or Metastatic Colorectal Cancer 영역에서 개발·상용화 중입니다. 작용기전: inhibits GC cell proliferation and induces apoptosis by regulating cell-cycle checkpoints and inhibiting oncogenic pathway. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 80% (ClinicalTrials.gov NCT04430738). 차별점: novel ternary copper-deferiprone-phenanthroline complex was rationally designed, synthesized, and thoroughly characterized.
Muscle Invasive Bladder Carcinoma
Advanced or Metastatic Colorectal Cancer
Recruiting
novel ternary copper-deferiprone-phenanthroline complex was rationally designed, synthesized, and thoroughly characterized
inhibits GC cell proliferation and induces apoptosis by regulating cell-cycle checkpoints and inhibiting oncogenic pathway
t cells to oxaliplatin (L-OHP) and 5-fluorouracil (5FU), an effect that was reversible upon PI3K pathway activation
DNA damage, with etoposide exhibiting the highest tail intensity (~60 %)
biomarker for metabolic state, B-cell/TLS-associated immune features, and vulnerability to DNA damage-based t
downregulation of PD-L1 via the IL-6/JAK/STAT3 pathway, reduction of immunosuppression, and promotion of immunogenic cell death (ICD)
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.