| Literature DB >> 20427244 |
Daniel Gaudet1, Janneke de Wal, Karine Tremblay, Stéphane Déry, Sander van Deventer, Andreas Freidig, Diane Brisson, Julie Méthot.
Abstract
Alipogene tiparvovec (AAV1-LPL(S447X)) gene therapy is developed to prevent complications and decrease the clinical morbidity of lipoprotein lipase deficiency (LPLD). LPLD is an autosomal recessive disease associated with severe hypertriglyceridemia (hyperTG), severe chylomicronaemia, and low HDL. Acute pancreatitis, the most frequent serious clinical LPLD complication, is a complex and heterogeneous inflammatory condition having many causes including hyperTG and chylomicronaemia. In many patients, low fat diet and currently available lipid lowering drugs are ineffective to prevent hyperTG or pancreatitis in LPLD. The clinical development program of alipogene tiparvovec includes observational studies as well as phase I/II and II/III clinical trials. Pooled data are collected on safety and efficacy issues, including the incidence of pancreatitis.Entities:
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Year: 2010 PMID: 20427244 DOI: 10.1016/j.atherosclerosissup.2010.03.004
Source DB: PubMed Journal: Atheroscler Suppl ISSN: 1567-5688 Impact factor: 3.235