Print ISSN:-2394-2789
Online ISSN:-2394-2797
CODEN : IJPCN9
Review Article
Author Details :
Volume : 11, Issue : 2, Year : 2024
Article Page : 136-140
https://doi.org/10.18231/j.ijpca.2024.018
Abstract
Alogliptin was initially approved to treat T2DM in Japan in 2010 and then approved by FDA and by EMA in 2013. Alogliptin, a highly potent and selective, noncovalent inhibitor of DPP-4. Inhibition of DPP-4 activity, alogliptin slows the inactivation of incretin hormones, glucagon-like peptide-1 (GLP-1). In terms of drug safety alogliptin is generally well-tolerated, with a low risk of hypoglycemia, weight gain, acute pancreatitis, and hepatotoxicity. Alogliptin has been effectively combined with Metformin or Pioglitazone to provide better glycaemic control. The drug can be used in mild hepatic or renal impairment with appropriate dosage adjustment. Treatment with alogliptin has shown less weight gain compared with sulfonylureas. Alogliptin and FDC of Alogliptin + Metformin approved and available in India with brand name Aloja & Aloja M/Forte, with well documented safety and efficacy through phase IV study conducted in India.
Keywords: DPP4i, T2DM, GLP1, GIP, atherogenic, lipids/adipose, tissue insulin resistance
How to cite : Tailokya A, Chaudhry S, Wawde G, Bhide Y, Inamdar K, Steps in discovery of alogliptin. Int J Pharm Chem Anal 2024;11(2):136-140
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