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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
brentuximab vedotin (Adcetris)
Seagen / Takeda·Hodgkin Disease
ORR 86%
ADCFDAPhase 3
Polatuzumab Vedotin (Polatuzumab Vedotin)
Roche / Genentech·FRα
ORR 95%·t½ 12.2 h
ADCPhase 2
Acalabrutinib (Acalabrutinib)
Epizyme, Inc.·Diffuse Large B-Cell Lymphoma
ORR 82.4%
Overview
Program
Brentuximab VedotinPolatuzumab VedotinAcalabrutinib
Overview
Company
Seagen / TakedaRoche / GenentechEpizyme, Inc.
Overview
Modality
ADCADCADC
Overview
Target
Hodgkin DiseaseFRαDiffuse Large B-Cell Lymphoma
Overview
Indication
Hodgkin LymphomaRelapsed or Refractory Follicular Lymphoma, Relapsed or Refractory Diffuse Large B-Cell LymphomaRelapsed Hematologic Malignancy; Refractory Hematologic Malignancy
Overview
Phase
APPROVEDPHASE_3PHASE_2
Overview
Status
ACTIVERECRUITINGRECRUITING
MoA
Mechanism
targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigentargeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigeninhibits B-cell receptor signaling
MoA
Biomarker
biomarker-driven treatment in NHL, including resistance mechanisms, toxicity management, optimal therapeuticCD20 expressionbiomarkers and inhibited the B-cell receptor pathway signaling in longitudinal samples from patients with rel
PK/PD
Half-life
12.2 h
PK/PD
Species
MouseRat, 048)Mouse
PK/PD
Animal (cat.)
Mouse, In vitroRatMouse, In vitro
PK/PD
Experiment
PDpharmacokineticPharmacokinetic
Toxicology
Species
Cynomolgus monkey, Mouse, RatCynomolgus monkey, Mouse, Rat, 048)Mouse, Rat
Toxicology
Animal (cat.)
Mouse, Rat, NHPMouse, Rat, NHPRat
Toxicology
Major finding
Hepatotoxicity : Monitor liver enzymes and bilirubin ( 5Hepatotoxicity: Monitor liver enzymes and bilirubinHepatotoxicity, Including Drug Induced Liver Injury: Monitor hepatic function throughout tr
Clinical
Primary efficacy
ORR 86%ORR 95%ORR 82.4%
Clinical
ORR
86%95.0%82.4%
Clinical
PFS
NA
Clinical
OS
NA
Clinical
Result source
ClinicalTrials.gov NCT01712490ClinicalTrials.gov NCT03677141ClinicalTrials.gov NCT03932331
Clinical
Data Tier / Score
B · 89S · 92C · 71
Clinical
Program phase
APPROVEDPHASE_3PHASE_2
Clinical
Clinical sync
2026년 7월 4일 (9일 전)2026년 7월 4일 (9일 전)2026년 7월 8일 (6일 전)