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Drug ReportsPagibaximab
Pagibaximab
Pagibaximab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
10 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Replacement arthroplasty kneeD019645—————1—1
Postoperative painD010149—G89.18———1—1
Acute kidney injuryD058186HP_0001919N17———1—1
Wounds and injuriesD014947—T14.8———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
SepsisD018805HP_0100806A41.9121——3
Birth weightD001724EFO_0004344—111——2
Staphylococcal infectionsD013203—A49.01—11——1
BacteremiaD016470EFO_0003033R78.81—11——1
ToxemiaD014115———11——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289———1———1
Lung neoplasmsD008175HP_0100526C34.90—1———1
Neonatal sepsisD000071074HP_0040187—11———1
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Surgical woundD000072836——————11
Breast neoplasmsD001943EFO_0003869C50————11
Drug therapyD004358——————11
MindfulnessD064866——————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePagibaximab
INNpagibaximab
Description
Pagibaximab (chimeric mab)
Classification
Antibody
Drug classmonoclonal antibodies
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL2108042
ChEBI ID—
PubChem CID—
DrugBank—
UNII ID23KB56UHN9 (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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