Lomitapide
| Clinical data | |
|---|---|
| Trade names | Juxtapid (US), Lojuxta (EU) | 
| Other names | AEGR-773, BMS-201038 | 
| License data | 
  | 
| Routes of administration  | By mouth | 
| ATC code | |
| Legal status | |
| Legal status | 
  | 
| Identifiers | |
  | |
| CAS Number | 
  | 
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | 
  | 
| ChemSpider | |
| UNII | 
  | 
| KEGG | |
| ChEBI | 
  | 
| ChEMBL | 
  | 
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C39H37F6N3O2 | 
| Molar mass | 693.734 g·mol−1 | 
| 3D model (JSmol) | |
  | |
  | |
| (what is this?) (verify) | |
Lomitapide , sold under the brand name Juxtapid in the US and Lojuxta in the EU, is a medication used as a lipid-lowering agent for the treatment of familial hypercholesterolemia, developed by Aegerion Pharmaceuticals. It has been tested in clinical trials as single treatment and in combinations with atorvastatin, ezetimibe and fenofibrate.
The US Food and Drug Administration (FDA) approved lomitapide in December 2012, as an orphan drug to reduce LDL cholesterol, total cholesterol, apolipoprotein B, and non-high-density lipoprotein (non-HDL) cholesterol in people with homozygous familial hypercholesterolemia (HoFH).
In July 2013, the European Commission approved lomitapide as an adjunct to a low-fat diet and other lipid-lowering medicinal products with or without low density lipoprotein (LDL) apheresis in adults with HoFH.