bamlanivimab

GPTKB entity

Statements (59)
Predicate Object
gptkbp:instance_of gptkb:monoclonal_antibody
gptkbp:approves gptkb:vaccine
November 2020
gptkbp:can_be_combined_with gptkb:etesevimab
gptkbp:clinical_trial gptkb:Europe
gptkb:Canada
gptkb:United_States
gptkb:National_Institutes_of_Health
gptkb:Eli_Lilly_and_Company
Phase 2
gptkbp:clinical_use combination therapy
monotherapy
gptkbp:collaborations government agencies
academic institutions
pharmaceutical companies
gptkbp:community_health improved patient outcomes
contributed to pandemic response
reduced burden on healthcare system
gptkbp:developed_by gptkb:Eli_Lilly_and_Company
gptkbp:dosage_form solution for infusion
gptkbp:duration single dose
gptkbp:funding public and private funding
https://www.w3.org/2000/01/rdf-schema#label bamlanivimab
gptkbp:indication mild to moderate COVID-19
gptkbp:invention gptkb:Eli_Lilly_and_Company
patented
gptkbp:market adverse event reporting
ongoing monitoring
safety studies
effectiveness studies
gptkbp:market_position available under EUA
gptkbp:marketed_as gptkb:Bamlanivimab
gptkbp:mechanism_of_action neutralizes virus
gptkbp:patient_population high-risk patients
gptkbp:pharmacokinetics half-life of approximately 20 days
gptkbp:provides_guidance_on gptkb:hospital
WHO recommendations
outpatient
CDC recommendations
gptkbp:received_emergency_use_authorization gptkb:FDA
gptkbp:regulatory_compliance Emergency Use Authorization
gptkbp:research_focus COVID-19 variants
gptkbp:research_output improved recovery time
reduced hospitalization
decreased viral load
reduced emergency visits
gptkbp:route_of_administration intravenous
gptkbp:safety_features generally well tolerated
gptkbp:side_effect fatigue
headache
nausea
diarrhea
infusion reactions
gptkbp:structure gptkb:Ig_G1
gptkbp:supply_chain limited availability
gptkbp:supply_status limited supply
gptkbp:targets gptkb:SARS-Co_V-2
gptkbp:bfsParent gptkb:imdevimab
gptkbp:bfsLayer 6