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Andexanet alfa
Ondexxya (andexanet alfa) is an unknown pharmaceutical. Andexanet alfa was first approved as Ondexxya on 2019-04-26. It is used to treat hemorrhage in the USA. It has been approved in Europe to treat drug-related side effects and adverse reactions.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
signs and symptoms pathological conditionsD013568
chemically-induced disordersD064419
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
Brand Name
Status
Last Update
andexxaBiologic Licensing Application2023-02-10
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
hemorrhageMP_0001914D006470R58
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
V03: All other therapeutic products
V03A: All other therapeutic products
V03AB: Antidotes
V03AB38: Andexanet alfa
HCPCS
No data
Clinical
Clinical Trials
15 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
Other
Total
HemorrhageD006470MP_0001914R581236
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients145
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 nameANDEXANET ALFA
INNandexanet alfa
Description
Andexanet alfa
Classification
Protein
Drug class
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID1262449-58-0
RxCUI
ChEMBL IDCHEMBL3301583
ChEBI ID
PubChem CID
DrugBankDB14562
UNII IDBI009E452R (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 788 documents
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Safety
Black-box Warning
Black-box warning for: Andexxa
Adverse Events
Top Adverse Reactions
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9,193 adverse events reported
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