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항목
ADCCurated CoreFDAstaleApproved
brentuximab vedotin (Adcetris)
Seagen / Takeda·Hodgkin Disease
180 trials
Overview
Program
Brentuximab Vedotin
Overview
Company
Seagen / Takeda
Overview
Modality
ADC
Overview
Target
Hodgkin Disease
Overview
Indication
Hodgkin's Disease
Overview
Phase
APPROVED
Overview
Status
APPROVED
Overview
Content status
Curated Core
Overview
Data Confidence
Data Confidence · High
Overview
Development Signal
Development Signal · Established
Overview
Approval status
FDA approved
Positioning
Key differentiator
Novel-Agent-Based Front-Line Therapy in Older Adults Aged ≥ 60 Years With Classic Hodgkin Lymphoma: A Systematic
Positioning
Known limitation
resistance mechanisms and improving outcomes in relapsed or refractory disease
Technology
Payload
vedotin and the anti-HER2 trastuzumab deruxteca
Technology
Linker
linker, or payload that have limited their development
MoA
Mechanism
targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigen
MoA
Biomarker
biomarker-driven treatment in NHL, including resistance mechanisms, toxicity management, optimal therapeutic
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
pharmacodynamic
Toxicology
Species
Cynomolgus monkey, Mouse, Rat
Toxicology
Animal (cat.)
Mouse, Rat, NHP
Toxicology
Major finding
Hepatotoxicity : Monitor liver enzymes and bilirubin ( 5
Clinical
Safety signal
Hepatotoxicity : Monitor liver enzymes and bilirubin ( 5
Clinical
Result source
ClinicalTrials.gov NCT01909934
Clinical
Program phase
APPROVED
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT01909934