Strensiq(asfotase alfa)
Strensiq (asfotase alfa) is an enzyme pharmaceutical. Asfotase alfa was first approved as Strensiq on 2015-08-28. It is used to treat hypophosphatasia in the USA. It has been approved in Europe to treat hypophosphatasia.
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Commercial
Trade Name
FDA
EMA
Strensiq
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Asfotase alfa
Tradename | Proper name | Company | Number | Date | Products |
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Strensiq | asfotase alfa | Alexion Pharmaceuticals | N-125513 RX | 2015-10-23 | 4 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
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strensiq | Biologic Licensing Application | 2020-06-22 |
Agency Specific
FDA
EMA
Expiration | Code | ||
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asfotase alfa, Strensiq, Alexion Pharmaceuticals, Inc. | |||
2122-10-23 | Orphan excl. |
Patent Expiration
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HCPCS
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Clinical
Clinical Trials
15 clinical trials
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | ASFOTASE ALFA |
INN | asfotase alfa |
Description | Asfotase alfa, sold under the brand name Strensiq, is a medication used in the treatment of people with perinatal/infantile- and juvenile-onset hypophosphatasia.
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Classification | Enzyme |
Drug class | enzymes |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL2108311 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB09105 |
UNII ID | Z633861EIM (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
Strensiq - Alexion Pharmaceuticals
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Strensiq - AstraZeneca
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 294 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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8,134 adverse events reported
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