Adcetris

GPTKB entity

Statements (58)
Predicate Object
gptkbp:instance_of gptkb:monoclonal_antibody
gptkbp:bfsLayer 6
gptkbp:bfsParent gptkb:Seagen
gptkbp:activities C D30-targeting antibody-drug conjugate
gptkbp:appointed_by healthcare professional
gptkbp:approves gptkb:2011
gptkb:U._S._Food_and_Drug_Administration
requires sterile water for injection
gptkbp:class antineoplastic agent
gptkbp:clinical_trial Phase 2
AETHERA
AVD regimen
BRIDGE study
ECHELON-1
ECHELON-2
monotherapy or in combination with chemotherapy
gptkbp:contraindication severe liver impairment
hypersensitivity to brentuximab vedotin
gptkbp:developed_by gptkb:Seattle_Genetics
gptkbp:dosage_form every 2 weeks
gptkbp:effective_date August 19, 2011
gptkbp:form injection
gptkbp:formulation lyophilized powder for reconstitution
https://www.w3.org/2000/01/rdf-schema#label Adcetris
gptkbp:indication relapsed or refractory systemic anaplastic large cell lymphoma
relapsed or refractory Hodgkin lymphoma
gptkbp:ingredients gptkb:brentuximab_vedotin
C6464 H10000 N1716 O2000 S40
gptkbp:interacts_with may interact with other immunosuppressants
gptkbp:invention patented
gptkbp:is_monitored_by liver function tests
complete blood count
neurological status
gptkbp:is_used_for treatment of Hodgkin lymphoma
treatment of systemic anaplastic large cell lymphoma
gptkbp:launch_date gptkb:2011
gptkbp:manager intravenous
gptkbp:manufacturer gptkb:Takeda_Pharmaceutical_Company
gptkbp:marketed_as gptkb:brentuximab_vedotin
gptkbp:packaging single-use vial
gptkbp:pharmacokinetics antibody-drug conjugate mechanism
half-life approximately 4 days
gptkbp:population adults and children over 2 years old
gptkbp:research_areas oncology
gptkbp:safety_features generally well tolerated
gptkbp:side_effect fatigue
nausea
liver toxicity
peripheral neuropathy
increased risk of infections
infusion reactions
neutropenia
pulmonary toxicity
tumor lysis syndrome
gptkbp:storage refrigerated
gptkbp:targets C D30
gptkbp:traded_on gptkb:Adcetris
gptkbp:weight approximately 150 k Da