Ultomiris

GPTKB entity

Statements (61)
Predicate Object
gptkbp:instance_of gptkb:monoclonal_antibody
gptkbp:activities complement inhibition
gptkbp:approves gptkb:FDA
gptkbp:availability consistent
gptkbp:class gptkb:drug
gptkbp:clinical_trial ongoing
Phase 3
immunosuppressive therapy
gptkbp:contraindication hypersensitivity to components
gptkbp:developed_by gptkb:Alexion_Pharmaceuticals
gptkbp:dosage_form none required
solution for infusion
gptkbp:duration ongoing
gptkbp:education important
gptkbp:effective_date December 2019
gptkbp:feedback generally favorable
gptkbp:formulation sterile liquid
gptkbp:frequency every 8 weeks
gptkbp:healthcare gptkb:battle
improving
necessary
https://www.w3.org/2000/01/rdf-schema#label Ultomiris
gptkbp:indication chronic kidney disease
gptkbp:ingredients gptkb:ravulizumab
gptkbp:interacts_with none significant known
gptkbp:invention patented
gptkbp:is_effective_against demonstrated
gptkbp:is_monitored_by complement levels
gptkbp:is_used_for treatment of paroxysmal nocturnal hemoglobinuria
treatment of atypical hemolytic uremic syndrome
gptkbp:lifespan approximately 15 days
gptkbp:manager intravenous
gptkbp:market global
gptkbp:marketed_as gptkb:Ultomiris
gptkbp:pharmacokinetics linear
complement inhibition
gptkbp:population adults and children over 1 year
gptkbp:price high
gptkbp:provides_information_on included
followed
gptkbp:receives_funding_from gptkb:stock_market_index
gptkbp:regulatory_compliance approved
gptkbp:research published
gptkbp:research_areas hematology
gptkbp:research_focus complement system
gptkbp:safety_features generally well tolerated
gptkbp:scholarships gptkb:stock_market_index
gptkbp:side_effect fatigue
headache
nausea
injection site reactions
serious infections
gptkbp:social_structure Ig G1 monoclonal antibody
gptkbp:storage refrigerated
gptkbp:supply_chain managed
gptkbp:treatment positive
gptkbp:type_of_care monitored
gptkbp:type_of_insurance varies
gptkbp:website vein
gptkbp:bfsParent gptkb:Alexion_Pharmaceuticals
gptkbp:bfsLayer 4