SWOG Cancer Research Network
Cyclin-Dependent Kinase 4 Inhibitor(SWOG Cancer Research Network)은 HER2 표적 ADC로, Anatomic Stage IV Breast Cancer AJCC v8; Metastatic HER2-Positive Breast Carcinoma 영역에서 개발·상용화 중입니다. 작용기전: TArgeting Chimera (PROTAC) estrogen receptor. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 19.2% (ClinicalTrials.gov NCT02499146). 차별점: first-in-class, selective, and orally bioavailable PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader.
HER2
Anatomic Stage IV Breast Cancer AJCC v8; Metastatic HER2-Positive Breast Carcinoma
Recruiting
oncolytic adenovirus reverses T cell exhaustion through the Rb-p65-CC
deruxtecan (T-DXd) and tyrosine kinase inhibitors
lentiviral knockdown experiments
humanized xenograft model and showed no evidence of significant off-target toxicity in immunocompetent hosts
first-in-class, selective, and orally bioavailable PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader
TArgeting Chimera (PROTAC) estrogen receptor
T-cell-inflamed microenvironment by providing a sustained chemotactic signal CCL5 for CD8+ T cell recruitment
apoptosis, associated with increased mRNA levels of positive regulators of cell cycle gene Cyclin E and proliferating cell nuclea
biomarker, Cyclin-dependent kinase 4 inhibitor A (p16INK4a)
resistance to ET, particularly caused by ESR1 mutations, has not been fully addressed
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
SWOG Cancer Research Network
Cyclin-Dependent Kinase 4 Inhibitor(SWOG Cancer Research Network)은 HER2 표적 ADC로, Anatomic Stage IV Breast Cancer AJCC v8; Metastatic HER2-Positive Breast Carcinoma 영역에서 개발·상용화 중입니다. 작용기전: TArgeting Chimera (PROTAC) estrogen receptor. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 19.2% (ClinicalTrials.gov NCT02499146). 차별점: first-in-class, selective, and orally bioavailable PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader.
HER2
Anatomic Stage IV Breast Cancer AJCC v8; Metastatic HER2-Positive Breast Carcinoma
Recruiting
oncolytic adenovirus reverses T cell exhaustion through the Rb-p65-CC
deruxtecan (T-DXd) and tyrosine kinase inhibitors
lentiviral knockdown experiments
humanized xenograft model and showed no evidence of significant off-target toxicity in immunocompetent hosts
first-in-class, selective, and orally bioavailable PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader
TArgeting Chimera (PROTAC) estrogen receptor
T-cell-inflamed microenvironment by providing a sustained chemotactic signal CCL5 for CD8+ T cell recruitment
apoptosis, associated with increased mRNA levels of positive regulators of cell cycle gene Cyclin E and proliferating cell nuclea
biomarker, Cyclin-dependent kinase 4 inhibitor A (p16INK4a)
resistance to ET, particularly caused by ESR1 mutations, has not been fully addressed
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.