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Press Release

Pooled analysis in adults with type 2 diabetes

Eli Lilly and Company
Posted on: 02 Oct 12

Pooled analysis in adults with type 2 diabetes presented at the 48th European Association for the Study of Diabetes (EASD) Annual Meeting

RIDGEFIELD, Conn. and INDIANAPOLIS, Oct. 2, 2012 /PRNewswire/ -- Boehringer Ingelheim Pharmaceuticals, Inc. and Eli Lilly and Company (NYSE: LLY) today announce data from a pooled analysis of two phase IIb trials in adults with type 2 diabetes (T2D) for an investigational SGLT-2 inhibitor, empagliflozin, at the 48th European Association for the Study of Diabetes (EASD) Annual Meeting in Berlin. The new analysis showed a reduction in systolic blood pressure with empagliflozin, which, in the study, was independent of the reductions observed in blood glucose or weight, based on a statistical measure called the Pearson correlation coefficient.1

Empagliflozin is part of a class of drugs being investigated for the reduction of blood glucose levels in adults with T2D. SGLT-2 inhibitors have been shown to reduce blood glucose, measured as hemoglobin A1c (HbA1c or A1C), by acting independently of insulin action. A1C is measured in people with diabetes to provide an index of blood glucose control for the previous two to three months.

"Most classes of currently available oral T2D treatments depend on the actions of the hormone insulin to lower elevated blood glucose. The emerging SGLT-2 inhibitor class removes glucose through the urine by blocking glucose re-absorption in the kidney," said Christophe Arbet-Engels, MD, PhD, MBA, vice president, metabolic-clinical development and medical affairs, Boehringer Ingelheim Pharmaceuticals, Inc. "Through the Boehringer Ingelheim and Lilly Diabetes Alliance, we are using our collective scientific expertise to address patient needs arising from the growing global diabetes epidemic. Together, we are committed to developing new medicines to address patients with this disease."

The pooled analysis includes data from two randomized, double-blind, placebo-controlled trials with treatment durations of 12 weeks (poster #770), assessing the safety and efficacy of empagliflozin alone (n=408) or as add-on to metformin (n=495) in adult patients with T2D. Patients were treated with either empagliflozin 10 mg or 25 mg.1 At week 12, the investigators assessed changes in both systolic and diastolic blood pressure, as well as calculated the Pearson correlation coefficients to measure whether changes in A1C or weight were related to changes in systolic blood pressure (SBP). Researchers also analyzed a subgroup of patients with an SBP > 140 mmHg at baseline.

At week 12, reductions in mean SBP of 3.8 mmHg and 4.5 mmHg were observed with empagliflozin 10 mg and 25 mg, respectively, versus 1.2 mmHg for placebo. Mean SBP at baseline of 131.3 mmHg and 132.5 mmHg were observed with empagliflozin 10 mg and 25 mg, respectively, versus 134.3 mmHg with placebo. For both dosages, this reduction in SBP was statistically significant compared to placebo. In patients with higher SBP at baseline ( > 140 mmHg), mean reductions of 17.0 mmHg and 13.4 mmHg were observed with empagliflozin 10 mg and 25 mg, respectively, and 10.4 mmHg with placebo.1

Reductions in diastolic blood pressure (DBP) were numerically greater with both empagliflozin doses compared to placebo, but the differences did not reach statistical significance. For the entire cohort, the reductions in DBP were 2.3 mmHg and 2.7 mmHg for empagliflozin 10mg and 25mg, respectively, and 1.8 mmHg for placebo.1 For patients with high DBP ( > 85 mmHg), reductions were 8.1 mmHg and 7.6 mmHg for empagliflozin 10mg and 25mg, respectively, and 6.1 mmHg for placebo.2

Overall, changes in systolic and diastolic blood pressure did not correlate with changes in pulse rate or A1C.1 The Pearson correlation coefficients between weight and SBP changes were 0.10 and 0.04 for empagliflozin 10 mg and 25 mg, respectively, and 0.12 for placebo. Between A1C and SBP changes, the coefficients were -0.09 and -0.02 for empagliflozin 10 mg and 25 mg, respectively, and 0.11 for placebo. None of these correlations reached statistical significance.1

"As many as two of three adults with diabetes have high blood pressure, which can raise the risk of other health complications in this population," said Carol Wysham, MD, Clinical Associate Professor of Medicine at the University of Washington School of Medicine. "It is important that we continue researching potential treatments that may help patients with type 2 diabetes control their blood glucose levels."

Adverse events (AEs) at week 12 were experienced by 34.2% and 31.6% of patients who received empagliflozin 10 mg and 25 mg, respectively, and by 34.6% who received placebo.1 The most commonly observed AEs included urinary tract and genital infections, generally categorized as mild, as seen in all clinical trials to date.2

Empagliflozin is being investigated in a phase III clinical trial program in adults with T2D with over 14,500 patients planned to be enrolled.2 There are 12 ongoing multinational phase III clinical trials, including a large cardiovascular outcome trial. Empagliflozin pivotal studies could complete in late 2012, with filing planned in the U.S. and Europe in 2013.

References
1.Hach T, Lambers Heerspink HJ, Pfarr E, et al. The sodium glucose cotransporter-2 (SGLT-2) inhibitor empagliflozin lowers blood pressure independent of weight or HbA1c changes. [Abstract #770]. Presented at the 48th European Association for the Study of Diabetes (EASD) Annual Meeting. October 1-5, Berlin.
2.Data on file, Boehringer Ingelheim Pharmaceuticals, Inc.

For more information:
http://newsroom.lilly.com/releasedetail.cfm?ReleaseID=710578

Editor's Details

Eli Lilly and Company
Eli Lilly and Company
http://newsroom.lilly.com/

Last updated on: 02/10/2012

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