Crysvita

GPTKB entity

Statements (61)
Predicate Object
gptkbp:instance_of gptkb:drug
gptkbp:bfsLayer 5
gptkbp:bfsParent gptkb:ALXN
gptkbp:activities anti-FG F23 monoclonal antibody
gptkbp:approves gptkb:2018
gptkb:FDA
gptkbp:clinical_trial Phase 3
pediatric patients
adult patients
NC T02915739
NC T02915753
NC T02915766
NC T02915780
NC T02915793
gptkbp:contraindication severe renal impairment
active infection
hypersensitivity to burosumab
gptkbp:current_use osteomalacia
hypophosphatemic rickets
renal phosphate wasting
gptkbp:developed_by gptkb:Ultragenyx_Pharmaceutical
gptkbp:dosage_form solution for injection
gptkbp:education recognizing side effects
proper injection technique
importance of regular monitoring
gptkbp:formulation sterile solution
gptkbp:frequency once a month
once every two weeks
https://www.w3.org/2000/01/rdf-schema#label Crysvita
gptkbp:indication X-linked hypophosphatemia in children
gptkbp:ingredients gptkb:burosumab
gptkbp:interacts_with no significant drug interactions reported
gptkbp:invention patented
gptkbp:is_monitored_by kidney function
calcium levels
serum phosphate levels
gptkbp:is_used_for treatment of X-linked hypophosphatemia
gptkbp:manager subcutaneous injection
gptkbp:marketed_as gptkb:legislation
gptkb:Japan
gptkb:United_States
gptkb:Native_American_tribe
gptkbp:packaging single-use prefilled syringe
gptkbp:pharmacokinetics half-life of approximately 19 days
elimination primarily through the reticuloendothelial system
peak plasma concentration at 1-3 days after injection
gptkbp:population adults
children aged 1 year and older
gptkbp:price varies by region
gptkbp:receives_funding_from covered by some insurance plans
gptkbp:side_effect gptkb:fandom
headache
injection site reactions
thrombocytopenia
serious allergic reactions
elevated liver enzymes
nasopharyngitis
hyperphosphatemia
gptkbp:status ongoing studies
gptkbp:storage refrigerated
gptkbp:type_of_care important for treatment efficacy