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Drug ReportsAlipogene tiparvovec
Alipogene tiparvovec
Glybera (alipogene tiparvovec) is a gene pharmaceutical. Alipogene tiparvovec was first approved as Glybera on 2012-10-25. It has been approved in Europe to treat hyperlipoproteinemia type i.
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Therapeutic Areas
Therapeutic Area
MeSH
hereditary congenital and neonatal diseases and abnormalitiesD009358
nutritional and metabolic diseasesD009750
Trade Name
FDA
EMA
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Drug Products
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
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Agency Specific
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ATC Codes
C: Cardiovascular system drugs
— C10: Lipid modifying agents
— C10A: Lipid modifying agents, plain
— C10AX: Other lipid modifying agents in atc
— C10AX10: Alipogene tiparvovec
HCPCS
No data
Clinical
Clinical Trials
3 clinical trials
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Indications Phases 4
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Indication
MeSH
Ontology
ICD-10
Ph 1
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Total
Hyperlipoproteinemia type iD008072Orphanet_411E78.3—32——3
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 nameAlipogene tiparvovec
INNalipogene tiparvovec
Description
Alipogene tiparvovec, sold under the brand name Glybera, is a gene therapy treatment designed to reverse lipoprotein lipase deficiency (LPLD), a rare recessive disorder, due to mutations in LPL, which can cause severe pancreatitis. It was recommended for approval by the European Medicines Agency in July 2012, and approved by the European Commission in November of the same year. It was the first marketing authorisation for a gene therapy treatment in either the European Union or the United States.
Classification
Gene
Drug class—
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID929881-05-0
RxCUI—
ChEMBL IDCHEMBL2108304
ChEBI ID—
PubChem CID—
DrugBankDB13521
UNII ID20OK4AFR4Y (ChemIDplus, GSRS)
Target
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Variants
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Financial
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Trends
PubMed Central
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Safety
Black-box Warning
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Adverse Events
0 adverse events reported
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