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Osocimab
Osocimab is an antibody pharmaceutical. It is currently being investigated in clinical studies. It is known to target coagulation factor XI.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
3 clinical trials
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Mock data
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Renal dialysisD006435EFO_0010690Z99.2112
Replacement arthroplasty kneeD01964511
Chronic kidney failureD007676EFO_0003884N18.611
ThromboembolismD013923HP_000190711
HemodiafiltrationD01758311
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameOSOCIMAB
INNosocimab
Description
Osocimab is an antibody pharmaceutical. It is currently being investigated in clinical studies. It is known to target coagulation factor XI.
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4297905
ChEBI ID
PubChem CID
DrugBank
UNII IDEK5V9UL3WL (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
F11
F11
Organism
Homo sapiens
Gene name
F11
Gene synonyms
NCBI Gene ID
Protein name
coagulation factor XI
Protein synonyms
coagualtion factor XI, Plasma thromboplastin antecedent, PTA
Uniprot ID
Mouse ortholog
F11 (109821)
coagulation factor XI (Q9DAT3)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
Mock data
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Additional graphs summarizing 53 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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