Tesaglitazar
From Wikipedia, the free encyclopedia
Tesaglitazar
|
|
Systematic (IUPAC) name | |
(2S)-2-Ethoxy-3-[4-[2-(4-methylsulfonyloxyphenyl)ethoxy]phenyl]propanoic acid | |
Identifiers | |
CAS number | |
ATC code | ? |
PubChem | |
Chemical data | |
Formula | C20H24O7S |
Mol. mass | 408.46 |
SMILES | & |
Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | ? |
Half life | ? |
Excretion | ? |
Therapeutic considerations | |
Pregnancy cat. |
? |
Legal status | |
Routes | ? |
Tesaglitazar is a proposed treatment 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]
[edit] 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: . PMID 17907109.
- ^ GALIDA™ (tesaglitazar) Clinical Trial Report Summaries. AstraZeneca. Retrieved on 2008-03-17.
- ^ AstraZeneca Discontinues Development of GALIDA (tesaglitazar). AstraZeneca (2006-05-04). Retrieved on 2008-03-17.
|