Tesaglitazar
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| Systematic (IUPAC) name | |
|---|---|
| (2S)-2-Ethoxy-3-[4-[2-(4-methylsulfonyloxyphenyl)ethoxy]phenyl]propanoic acid | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 251565-85-2 |
| ATC code | None |
| PubChem | CID 208901 |
| UNII | 6734037O3L |
| KEGG | D01274 |
| ChEMBL | CHEMBL521632 |
| Chemical data | |
| Formula | C20H24O7S |
| Mol. mass | 408.46 |
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Tesaglitazar (AZ 242) is a peroxisome proliferator-activated receptor agonist with affinity to PPARα and PPARγ, proposed for type 2 diabetes.1
The drug had completed several phase III clinical trials,2 however in May, 2006 AstraZeneca announced that it had discontinued further development.3
References
- ^ Wilding JP, Gause-Nilsson I, Persson A (2007). "Tesaglitazar, as add-on therapy to sulphonylurea, dose-dependently improves glucose and lipid abnormalities in patients with type 2 diabetes". Diab Vasc Dis Res 4 (3): 194–203. doi:10.3132/dvdr.2007.040. PMID 17907109.
- ^ "GALIDA (tesaglitazar) Clinical Trial Report Summaries". AstraZeneca. Retrieved 2008-03-17.dead link
- ^ "AstraZeneca Discontinues Development of GALIDA (tesaglitazar)". AstraZeneca. 2006-05-04. Retrieved 2012-07-23.
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