Key result
Balaglitazone 10 mg and 20 mg provided robust glycemic control, significantly reducing HbA1c compared to pioglitazone 45 mg, with a lower incidence of fluid retention and fat accumulation.
Why the study?
Does balaglitazone improve glycemic control and safety compared to pioglitazone in patients on insulin therapy?
Does balaglitazone improve glycemic control and safety compared to pioglitazone in patients on insulin therapy?
Balaglitazone is a novel partial PPAR-gamma agonist that provides robust glycemic control comparable to pioglitazone but with a potentially better safety profile regarding fluid retention and cardiovascular events.
May support balaglitazone for insulin-treated diabetes with fewer side effects; hypothesis-generating pending dedicated RCTs.
Balaglitazone (DRF-2593) is a novel partial agonist of PPAR-gamma (γ), which is developed by Dr. Reddy's laboratories India. Balaglitazone is a second generation peroxisome proliferator-activated receptor (PPAR) gamma agonist with only partial agonistic properties. Balaglitazone is currently being evaluated in phase III clinical trial in United States and Europe. Selective PPAR-γ modulators bind in distinct manners to the ligand-binding pocket of PPAR-γ, leading to alternative receptor conformations, differential cofactor recruitment/displacement, differential gene expression, and ultimately differential biological responses. Based on this concept, new and improved novel antidiabetic agents are in current development. Clinical studies conducted with 409 subjects of randomized, double blind, parallel-group placebo and active comparator-controlled subject groups to determine the efficacy and safety of Balaglitazone. The study showed that the trial met its primary endpoint. Balaglitazone treated groups shown significantly reduce of HbA1c (%), FSG (mmol/L), postprandial glucose as comparison to pioglitazone. Phase III clinical studies data clearly shows that Balaglitazone provides robust glycemic control as an add-on to insulin therapy. Balaglitazone 10 mg and 20 mg show the similar magnitudes of the effects which comparable to the effects seen in the pioglitazone 45 mg group. The incidence of fluid retention and fat accumulation fewer than those observed with pioglitazone 45 mg. Hence, Balaglitazone is prominent candidate of new glitazone which requires fewer doses as comparison pioglitazone and shows better safety profile less incidence of special adverse effect like heart failure, peripheral oedema, and myocardial infarction. Unlike other marketed PPAR gamma agonists, Balaglitazone shows less fluid retention, less heart enlargement and no reduction of bone formation than full PPAR gamma agonists in preclinical studies. In present review, we have tried to cover classification PPARs various ligands, chemistry, physical properties, commercial synthesis, current patent status, polymorphic information, receptor interaction, pharmacophore rational, mechanism, adverse effect and clinical status of Balaglitazone, giving emphasis on medicinal chemistry aspect.
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Agrawal et al. (2012) conducted a review in Diabetes (n=409). Balaglitazone vs. Placebo and pioglitazone 45 mg was evaluated on HbA1c (%), FSG (mmol/L), and postprandial glucose. Balaglitazone 10 mg and 20 mg provided robust glycemic control, significantly reducing HbA1c compared to pioglitazone 45 mg, with a lower incidence of fluid retention and fat accumulation.
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