Atezolizumab + Bevacizumab(Roche / Genentech)은 Gastric Adenocarcinoma 표적 항체로, Venous Thrombosis 영역에서 개발·상용화 중입니다. 작용기전: bispecific antibody elicited strong antitumor activity mediated by intratumoral recruitment and activation of T cells. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 49.3% (ClinicalTrials.gov NCT02366143). 차별점: unique EM, 29% had ≥ 2 EM sites and 8.
Gastric Adenocarcinoma
Venous Thrombosis
Recruiting
bispecific antibody elicited strong antitumor activity mediated by int
humanized HCC xenograft mouse model recapitulating the GPC3-high progenitor-like subtype, a GPC3/CD3 bispecif
unique EM, 29% had ≥ 2 EM sites and 8
bispecific antibody elicited strong antitumor activity mediated by intratumoral recruitment and activation of T cells
biomarkers in several malignancies; however, their role in patients receiving avelumab maintenance for advanc
resistance to the target therapy
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.
Atezolizumab + Bevacizumab(Roche / Genentech)은 Gastric Adenocarcinoma 표적 항체로, Venous Thrombosis 영역에서 개발·상용화 중입니다. 작용기전: bispecific antibody elicited strong antitumor activity mediated by intratumoral recruitment and activation of T cells. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 49.3% (ClinicalTrials.gov NCT02366143). 차별점: unique EM, 29% had ≥ 2 EM sites and 8.
Gastric Adenocarcinoma
Venous Thrombosis
Recruiting
bispecific antibody elicited strong antitumor activity mediated by int
humanized HCC xenograft mouse model recapitulating the GPC3-high progenitor-like subtype, a GPC3/CD3 bispecif
unique EM, 29% had ≥ 2 EM sites and 8
bispecific antibody elicited strong antitumor activity mediated by intratumoral recruitment and activation of T cells
biomarkers in several malignancies; however, their role in patients receiving avelumab maintenance for advanc
resistance to the target therapy
차트 로드 중…
임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.
수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.