Alipogene Tiparvovec

drug
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Also known as Alipogen tiparvovecGlybera

Summary

Alipogene Tiparvovec (CHEMBL2108304) is an approved gene (ATC C10AX10); indicated across 2 conditions including cardiovascular disorder and familial lipoprotein lipase deficiency.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Gene
  • ATC class: C10AX10
  • Indications: 2 conditions
  • Clinical trials: 3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108304
NameAlipogene Tiparvovec
TypeGene
Max phase4
ATCC10AX10

Also known as: Alipogen tiparvovec, Alipogene tiparvovec, Glybera, ALIPOGENE TIPARVOVEC

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
cardiovascular disorder4MONDO:0004995EFO:0000319
familial lipoprotein lipase deficiency4MONDO:0009387MONDO:0009387

Clinical trials

Total trials: 3.

Phase distribution

PhaseTrials
PHASE2/PHASE32
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00891306PHASE2/PHASE3COMPLETEDEfficacy and Safety of Human Lipoprotein Lipase (LPL)[S447X] Expressed by an Adeno-Associated Viral Vector in LPL-deficient Subjects
NCT01109498PHASE2/PHASE3UNKNOWNSafety and Efficacy in LPL-Deficient Subjects of AMT-011, an Adeno-Associated Viral Vector Expressing Human Lipoprotein Lipase [S447X]
NCT02904772PHASE2WITHDRAWNAlipogene Tiparvovec for the Treatment of LPLD Patients

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).