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프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-13 · 마지막 7월 13일

현재 선택: 3 · Data Tier에서 열림

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV24행 · 3개 프로그램

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항목
ADCFDAApproved
belantamab mafodotin (Blenrep, GSK2857916)
GSK·BCMA
ORR 31%·t½ 16.8 h
ADCPhase 2
Cytoxan (Cytoxan)
Merck Sharp & Dohme LLC·Metastatic Breast Cancer
ORR 95%
ADCPhase 2
Sirolimus (Sirolimus)
Christopher Strouse·FRα
ORR 9%
Overview
Program
Blenrep (belantamab mafodotin)CytoxanSirolimus
Overview
Company
GSKMerck Sharp & Dohme LLCChristopher Strouse
Overview
Modality
ADCADCADC
Overview
Target
BCMAMetastatic Breast CancerFRα
Overview
Indication
Multiple myelomaMultiple Myeloma, RefractoryMultiple Myeloma
Overview
Phase
APPROVEDPHASE_2PHASE_2
Overview
Status
DISCONTINUEDRECRUITINGDISCONTINUED
MoA
Mechanism
BCMA binding → MMAF payload deliverytargeted metabolomics analysis based on UPLC-MS/MS and a reverse transcription polymerase chain reaction (RT-qPCR) technology were used to explore the specific metabolic pathwaytarget synergy, effectively inhibits the PI3K pathway
MoA
Biomarker
BCMA expressionEGFR gene exhibited the high
PK/PD
Half-life
16.8 h
PK/PD
Species
Cynomolgus monkey, HumanMouseMouse, Human
PK/PD
Animal (cat.)
Human, NHPMouseHuman, Mouse, In vitro
PK/PD
Experiment
PharmacokineticPKpharmacokinetic
Toxicology
Species
Cynomolgus monkey, Mouse, Rat, HumanMouseMouse, Rat, Hamster, Human
Toxicology
Animal (cat.)
Mouse, RatMouseMouse, Rat
Toxicology
Major finding
hepatotoxicity, eye pain, diarrhea, fatigue, pneumonia, cataract, and COVID-19A CD45-targeted antibody-drug conjugate successfully conditions for allogeneic hematopoietic stem cell transplantation in mice.. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment of patients with nonmalignant or malignant blood disorders. Its success has been limited by graft-versus-host disease (GVHD). Current systemic nontargeted conditioning regi…Hepatotoxicity, including fatal hepatic necrosis, with elevated sirolimus trough concentrat
Toxicology
CRS
grade 4
Clinical
Primary efficacy
ORR 31%ORR 95%ORR 9%
Clinical
ORR
31% (DREAMM-2)95.0%9%
Clinical
PFS
2.9 mo
Clinical
Result source
DREAMM-2ClinicalTrials.gov NCT03677141ClinicalTrials.gov NCT02357342
Clinical
Data Tier / Score
S · 64B · 62C · 16
Clinical
Program phase
APPROVEDPHASE_2PHASE_2
Clinical
Clinical sync
2026년 7월 8일 (6일 전)2026년 7월 9일 (5일 전)2026년 7월 8일 (6일 전)