Tafasitamab

GPTKB entity

Statements (57)
Predicate Object
gptkbp:instanceOf monoclonal antibody
gptkbp:administrativeDivision once weekly for the first 8 weeks
gptkbp:approves gptkb:FDA
gptkbp:associatedWith oncology
hematology
immunotherapy
monoclonal antibody therapy
gptkbp:availableIn gptkb:Australia
gptkb:Canada
gptkb:Japan
gptkb:United_States
gptkbp:chemicalFormula IgG1 subclass
gptkbp:clinicalTrials Phase 2
multiple centers worldwide
Phase 3 ongoing
monotherapy or in combination therapy
increased progression-free survival
L-MIND trial
improved overall response rate
gptkbp:contraindication hypersensitivity to tafasitamab
gptkbp:culturalEvents not_yet_approved_in_Europe
gptkbp:developedBy gptkb:MorphoSys_AG
gptkbp:dosageForm solution for infusion
gptkbp:drugInterdiction antibody-dependent cellular cytotoxicity
half-life of approximately 12 days
gptkbp:followedBy once every 2 weeks
gptkbp:hasPopulation adults
gptkbp:healthcare relapsed or refractory DLBCL
gptkbp:historical_analysis ongoing studies for other cancers
https://www.w3.org/2000/01/rdf-schema#label Tafasitamab
gptkbp:impact until disease progression or unacceptable toxicity
gptkbp:interactsWith live vaccines
gptkbp:is_monitored_by complete blood counts
gptkbp:issuedBy intravenous infusion
gptkbp:isTaskedWith other immunosuppressive agents
gptkbp:lastProduced 2020
gptkbp:mandates B-cell malignancies
gptkbp:marketedAs gptkb:Incyte_Corporation
brand_name_Monjuvi
gptkbp:origin humanized
gptkbp:partnerships gptkb:Incyte_Corporation
gptkbp:patentStatus patented
gptkbp:patentType June 2020
gptkbp:regulatoryCompliance approved
gptkbp:researchFocus B-cell lymphomas
CD19 targeting therapies
gptkbp:route IV
gptkbp:safetyFeatures generally well tolerated
gptkbp:sideEffect fatigue
nausea
diarrhea
infections
cytopenia
gptkbp:targets CD19
gptkbp:triggerType targets CD19
gptkbp:usedFor treatment of relapsed or refractory diffuse large B-cell lymphoma
gptkbp:variant lenalidomide