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Drug ReportsCosfroviximab
Cosfroviximab
Cosfroviximab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
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FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
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Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
16 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
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Total
Ebola hemorrhagic feverD019142EFO_0007243A98.41212
Virus diseasesD014777B34111
EbolavirusD029043111
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
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Total
InfectionsD007239EFO_0000544111
Communicable diseasesD003141111
Indications Phases 1
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MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
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Total
Healthy volunteers/patients44
Alzheimer diseaseD000544EFO_0000249F03112
InflammationD007249MP_000184511
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
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Total
TauopathiesD02480122
Frontotemporal dementiaD057180HP_0002145G31.011
Progressive supranuclear palsyD013494EFO_0002512G23.111
Primary progressive aphasiaD018888EFO_0009053G31.0111
Pick disease of the brainD020774EFO_0003096G31.0111
Corticobasal degenerationD00008828211
MalnutritionD044342EFO_0008572E40-E4611
Protein-energy malnutritionD011502EFO_0009563E4111
Central nervous system diseasesD002493HP_0002011G96.911
Brain diseasesD001927HP_0001298G93.4011
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCosfroviximab
INNcosfroviximab
Description
ZMapp is an experimental biopharmaceutical drug comprising three chimeric monoclonal antibodies under development as a treatment for Ebola virus disease. Two of the three components were originally developed at the Public Health Agency of Canada's National Microbiology Laboratory (NML), and the third at the U.S. Army Medical Research Institute of Infectious Diseases; the cocktail was optimized by Gary Kobinger, a research scientist at the NML and underwent further development under license by Mapp Biopharmaceutical. ZMapp was first used on humans during the Western African Ebola virus epidemic, having only been previously tested on animals and not yet subjected to a randomized controlled trial. The National Institutes of Health (NIH) ran a clinical trial starting in January 2015 with subjects from Sierra Leone, Guinea, and Liberia aiming to enroll 200 people, but the epidemic waned and the trial closed early, leaving it too statistically underpowered to give a meaningful result about whether ZMapp worked.
Classification
Antibody
Drug classmonoclonal antibodies
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Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL3990001
ChEBI ID
PubChem CID
DrugBank
UNII ID820CI2BHRP (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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