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항목
ADCStandard DatabasestalePreclinical
Genetical Recombination (Brentuximab Vedotin, Brentuximab Vedotin (Genetical Recombination))
Seagen / Takeda·Peripheral T Cell Lymphoma
93 trials
Overview
Program
Brentuximab Vedotin (Genetical Recombination)
Overview
Company
Seagen / Takeda
Overview
Modality
ADC
Overview
Target
Peripheral T Cell Lymphoma
Overview
Indication
Untreated CD30-Positive Hodgkin's Lymphoma
Overview
Phase
PRECLINICAL
Overview
Status
ACTIVE
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Watch
Overview
Approval status
Investigational
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
biomarkers for HBsAg clearance and responses to Peg-IFN-α in HBeAg-negative chronic hepatitis B patient
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
pd
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Effectiveness and safety of brentuximab vedotin-containing regimen versus standard chemotherapy in relapsed or refractory Hodgkin lymphoma: a multicenter cohort study.. Hodgkin lymphoma (HL) constitutes 3.4% of all cancers in Saudi Arabia, with advanced-stage relapse rates reaching 40%. While the anti-CD30 agent brentuximab vedotin (BV) has established efficacy, local data are limited. This study …
Clinical
Safety signal
Effectiveness and safety of brentuximab vedotin-containing regimen versus standard chemotherapy in relapsed or refractory Hodgkin lymphoma: a multicenter cohort study.. Hodgkin lymphoma (HL) constitutes 3.4% of all cancers in Saudi Arabia, with advanced-stage relapse rates reaching 40%. While the anti-CD30 agent brentuximab vedotin (BV) has established efficacy, local data are limited. This study …
Clinical
Selected reported efficacy
ORR 89.5%
Clinical
Reported ORR
89.5%
Clinical
Result source
ClinicalTrials.gov NCT02588651
Clinical
Program phase
PRECLINICAL
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT02588651