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ADCPhase 3Recruiting

belantamab mafodotin (Blenrep, GSK2857916)

GSK

비교

Belantamab mafodotin(GSK)은 Multiple Myeloma 표적 ADC로, Multiple Myeloma 영역에서 개발·상용화 중입니다. 작용기전: targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigen. Phase 3 후기 임상 단계입니다. 대표 임상 효능: ORR 100% (ClinicalTrials.gov NCT03828292). PK: t½ 16.8 h. 차별점: unique toxicities related to the antigen target, linker, or payload that have limited their development.

출처: ClinicalTrials.gov · PubMed · openFDA최근 동기화됨

개요

임상 2026년 7월 6일 (8일 전)PK/독성 2026년 7월 6일 (8일 전)

Multiple Myeloma

Multiple Myeloma

Recruiting

Technology

ADCs) represent an important therapeutic modality for the treat

cys-mcMMAF

linker, or payload that have limited their development

humanized anti-B-cell maturation antigen (BCMA) monoclonal antibody conjugated to monomethyl auristatin F (MM

unique toxicities related to the antigen target, linker, or payload that have limited their development

Mechanism of Action

targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigen

cytokine release syndrome, all grade 1

payload (cys-mcMMAF) pharmacokinetics

biomarkers and biologic profiling to enable optimal, integrated use of mAbs, ADCs, CAR T-cell therapies, and

bypass this immune effector cell dependence, we developed a novel strategy using antibody-drug conjugates (ADCs)

임상시험 & 결과

차트 로드 중…

임상 한눈에 보기

  • 69건의 ClinicalTrials.gov 임상 기록
  • Phase·Status 요약은 enrollment 상위 표본 기준입니다
  • 임상시험 탭에서 enrollment 상위 목록을 불러올 수 있습니다
  • Phase: Phase 3 · Phase 1, Phase 2 · Phase 2
  • Status: Completed · Recruiting · Active, not recruiting
  • 주요 endpoint: Sepsis-related toxicity of antibody-drug conjugate. · Causality assessment of reported cardiovascular events according to the WHO system · Description of the type of sepsis-related toxicities depending on the category of ADC · Description of the drug-drug interactions associated with sepsis-related adverse events · Description of the population of patients having a sepsis-related adverse events
  • 등록된 결과: ORR 100%
  • 핵심: Belantamab mafodotin (GSK2857916) is a first in class, antibody dependent cellular cytotoxicity (ADCC) enhanced, humaniz…

임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.

수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.

참고문헌

자주 묻는 질문

Belantamab mafodotin은 어떤 치료제인가요?
Belantamab mafodotin(GSK)은 Multiple Myeloma 표적 ADC로, Multiple Myeloma 영역에서 개발·상용화 중입니다. 데이터는 바이오모아 (BioMoa)에서 ClinicalTrials.gov·openFDA·PubMed 기반으로 정리합니다.
Belantamab mafodotin의 임상 단계는?
Belantamab mafodotin의 현재 단계는 Phase 3입니다.
비슷한 프로그램과 어떻게 비교하나요?
바이오모아 (BioMoa) 비교 페이지에서 PK/PD, 독성, 임상 효능 지표를 나란히 볼 수 있습니다. 동일 타깃·모달리티 프리셋을 함께 참고하세요.