Bamlanivimab

GPTKB entity

Statements (64)
Predicate Object
gptkbp:instance_of gptkb:monoclonal_antibody
gptkbp:administration_duration 1 hour
gptkbp:approves gptkb:FDA
November 2020
gptkbp:associated_with COVID-19 variants
gptkbp:average_temperature 2 to 8 degrees Celsius
gptkbp:can_be_combined_with gptkb:Etesevimab
gptkbp:clinical_trial gptkb:Europe
gptkb:Canada
gptkb:United_States
gptkb:Eli_Lilly_and_Company
Phase 2
Phase 3
improved recovery
reduced hospitalization
reduced emergency visits
gptkbp:clinical_use combination therapy
monotherapy
gptkbp:contraindication severe allergic reactions
hypersensitivity
gptkbp:developed_by gptkb:Eli_Lilly_and_Company
gptkbp:dosage_form gptkb:Software_Solutions
solution for infusion
700 mg
https://www.w3.org/2000/01/rdf-schema#label Bamlanivimab
gptkbp:indication mild to moderate COVID-19
gptkbp:invention patented
gptkbp:market_position hospital settings
available in pharmacies
gptkbp:marketed_as gptkb:Bamlanivimab_injection
gptkbp:mechanism_of_action neutralizes virus
neutralizes SARS-Co V-2
gptkbp:patient_population adults
high-risk patients
pediatric patients
gptkbp:pharmacokinetics Ig G1 monoclonal antibody
half-life 15 days
gptkbp:provides_guidance_on WHO recommendations
CDC guidelines
gptkbp:publication peer-reviewed journals
scientific articles
clinical trial reports
gptkbp:research_areas pharmacology
infectious diseases
immunology
gptkbp:route_of_administration intravenous
gptkbp:safety_measures post-marketing surveillance
adverse event tracking
clinical safety assessments
gptkbp:shelf_life 24 months
gptkbp:side_effect fatigue
headache
nausea
diarrhea
mandatory reporting
infusion reactions
gptkbp:storage 2 to 8 degrees Celsius
gptkbp:suitable_for severe COVID-19
gptkbp:targets gptkb:SARS-Co_V-2
gptkbp:trade gptkb:Bamlanivimab
gptkbp:used_for gptkb:vaccine
treatment of COVID-19
gptkbp:bfsParent gptkb:Lilly's_COVID-19_antibody_therapy
gptkbp:bfsLayer 5