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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

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

API CSV26행 · 3개 프로그램

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항목
ADCFDAApproved
trastuzumab deruxtecan (Enhertu, T-DXd, DS-8201)
Daiichi Sankyo / AstraZeneca·HER2
ORR 79.7%·t½ ~5.8 days (ADC)
ADCFDAApproved
disitamab vedotin (Disitamab Vedotin, RC48)
RemeGen·HER2
ORR 50%·t½ ~5 days
Overview
Program
Enhertu (trastuzumab deruxtecan)Disitamab Vedotin (RC48)5-FU, leucovorin, docetaxel, oxaliplatin (FLOT)
Overview
Company
Daiichi Sankyo / AstraZenecaRemeGenYu jiren
Overview
Modality
ADCADCANTIBODY
Overview
Target
HER2HER2HER2
Overview
Indication
HER2+ breast cancer, HER2-low, gastricHER2+ urothelial, gastric, breastAdenocarcinoma of the Stomach; Adenocarcinoma of Esophagogastric Junction
Overview
Phase
APPROVEDAPPROVEDPHASE_2
Overview
Status
APPROVEDACTIVERECRUITING
MoA
Mechanism
HER2-mediated internalization → DXd release → DNA damageHER2-mediated delivery of MMAE
MoA
Biomarker
HER2 IHC/ISHHER2 expression
PK/PD
Half-life
~5.8 days (ADC)~5 days
PK/PD
Species
Mouse, Human, Tumor shrinkage, HER2 pathway suppressionMouseMouse, Toxicity is manageable across all arms
PK/PD
Animal (cat.)
Human, Mouse, In vitroMouse, In vitroMouse
PK/PD
Experiment
PDPDPD
Toxicology
Species
Cynomolgus monkey, Mouse, Rat, Hamster, HumanMouseMouse, Toxicity is manageable across all arms
Toxicology
Animal (cat.)
NHPMouse, In vitroMouse
Toxicology
Major finding
ILD-like lung findings at high exposurethrombocytopenia, demonstrated for Kadcyla and EnhertuPerioperative FLOT Chemotherapy in Resectable Gastric Adenocarcinoma: A Single-center Retrospective Observational Study.. Gastric cancer (GC) is a leading cause of cancer-related mortality worldwide. Perioperative chemotherapy improves tumor downstaging and survival rates. The FLOT regimen was proven superior in the FLOT4-AIO trial, establishing it as the standard care for resectable gastric adeno…
Toxicology
CRS
Minimal
Clinical
Primary efficacy
ORR 79.7%ORR 50%ORR 23.1%
Clinical
ORR
79.7%~50% in HER2+ UC23.1%
Clinical
PFS
NA6.9 mo
Clinical
OS
NA8.97
Clinical
Result source
ClinicalTrials.gov NCT03529110RC48-C009ClinicalTrials.gov NCT00382720
Clinical
Data Tier / Score
S · 100B · 89C · 46
Clinical
Program phase
APPROVEDAPPROVEDPHASE_2
Clinical
Dose / schedule
q3wq2w
Clinical
Clinical sync
2026년 7월 8일 (6일 전)2026년 7월 8일 (6일 전)2026년 7월 6일 (8일 전)