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프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-8 · 마지막 7월 21일

현재 선택: 5 · 임상 갱신 필요 3 · Data Tier에서 열림

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

API CSV25행 · 5개 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 100%·t½ 12.2 h
AntibodystalePhase 3
Zanubrutinib (Zanubrutinib)
Juan P. Alderuccio, MD·CNS Lymphoma
ORR 95.2%
AntibodystalePhase 3
lymphodepleting chemotherapy (lymphodepleting chemotherapy)
Hemogenyx Pharmaceuticals LLC·Non-Hodgkin Lymphoma
ORR 80.3%
ADCstalePhase 2
Acalabrutinib (Acalabrutinib)
Epizyme, Inc.·Diffuse Large B-Cell Lymphoma
ORR 82.4%
Overview
Program
Brentuximab VedotinPolatuzumab VedotinZanubrutiniblymphodepleting chemotherapyAcalabrutinib
Overview
Company
Seagen / TakedaRoche / GenentechJuan P. Alderuccio, MDHemogenyx Pharmaceuticals LLCEpizyme, Inc.
Overview
Modality
ADCADCANTIBODYANTIBODYADC
Overview
Target
Hodgkin DiseaseFRαCNS LymphomaNon-Hodgkin LymphomaDiffuse Large B-Cell Lymphoma
Overview
Indication
Hodgkin LymphomaRelapsed or Refractory Follicular Lymphoma, Relapsed or Refractory Diffuse Large B-Cell LymphomaCNS LymphomaClear Cell Carcinoma; Phase 1Relapsed Hematologic Malignancy; Refractory Hematologic Malignancy
Overview
Phase
APPROVEDPHASE_3PHASE_3PHASE_3PHASE_2
Overview
Status
ACTIVERECRUITINGRECRUITINGACTIVERECRUITING
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 signalingCAR-T cell therapy for GAD65 antibody-mediated cerebellar ataxiainhibits B-cell receptor signaling
MoA
Biomarker
biomarker-driven treatment in NHL, including resistance mechanisms, toxicity management, optimal therapeuticCD20 expressionbiomarker to guide treatment duration in two prospective trials of venetoclax- and sonrotoclax-based tripletsbiomarkers exist to predict toxicity risk, underscoring the need for further researchbiomarkers 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
MouseRatRatMouseMouse
PK/PD
Animal (cat.)
Mouse, In vitroRat, In vitroRatMouseMouse, In vitro
PK/PD
Experiment
pdpharmacokineticPKPDPharmacokinetic
Toxicology
Species
Cynomolgus monkey, Mouse, RatCynomolgus monkey, Mouse, RatRatMouseMouse, Rat
Toxicology
Animal (cat.)
Mouse, Rat, NHPMouse, Rat, NHPRatMouseRat
Toxicology
Major finding
Hepatotoxicity : Monitor liver enzymes and bilirubin ( 5Hepatotoxicity: Monitor liver enzymes and bilirubinHepatotoxicity, Including Drug-Induced Liver Injury : Monitor hepatic function throughout tthrombocytopenia) but achieved a best response of morphologic leukemia-free state on day 14 follHepatotoxicity, Including Drug Induced Liver Injury: Monitor hepatic function throughout tr
Toxicology
CRS
Reported
Clinical
Primary efficacy
ORR 86%ORR 100%ORR 95.2%ORR 80.3%ORR 82.4%
Clinical
ORR
86%100.0%95.2%80.3%82.4%
Clinical
PFS
61.49.03NA
Clinical
OS
NANANA
Clinical
Result source
ClinicalTrials.gov NCT01712490ClinicalTrials.gov NCT02611323ClinicalTrials.gov NCT02343120ClinicalTrials.gov NCT03483103ClinicalTrials.gov NCT03932331
Clinical
Data Tier / Score
A · 89S · 92B · 78C · 75C · 71
Clinical
Program phase
APPROVEDPHASE_3PHASE_3PHASE_3PHASE_2
Clinical
Clinical sync
2026년 7월 18일 (8일 전)2026년 7월 18일 (8일 전)2026년 7월 8일 (19일 전 · 갱신 권장)2026년 7월 9일 (18일 전 · 갱신 권장)2026년 7월 8일 (19일 전 · 갱신 권장)