Conference Coverage

Canagliflozin effects include weight loss in phase III placebo-controlled trial


 

FROM AACE 2014

Treatment with canagliflozin was associated with significant weight loss as well as improvements in glycemic control, when compared with placebo in a 26-week, phase III study of nearly 600 patients.

Dr. William Canovatchel of Janssen Pharmaceuticals, the manufacturer of canagliflozin, is presenting these results on May 16 at the annual meeting of the American Association of Clinical Endocrinologists.

In phase III clinical trials, canagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, has been associated with significant weight loss in a variety of patients, he noted. In the phase III randomized, placebo-controlled study, 584 patients with type 2 diabetes who were inadequately treated with diet and exercise were randomized to placebo or canagliflozin (300 mg or 100 mg once a day). The mean age was 55 years, and the patients’ mean hemoglobin A1c was 8%. Their mean body weight was 191 pounds (86.8 kg).

At 26 weeks, the mean reductions in HbA1c from baseline (the primary endpoint) among patients on the 100-mg and 300-mg doses of canagliflozin were 0.77% and 1.03%, respectively, compared with an increase of 0.14% among those on placebo. Differences between the drug and placebo were statistically significant.

In addition, those on the 100-mg and 300-mg canagliflozin doses lost a mean of 5.5 pounds (2.5 kg), and 7.5 pounds (3.4 kg), respectively, compared with a mean of 1 pound (0.5 kg) among those on placebo.

Moreover, 71% of those on 100 mg and 84% of those on 300 mg had reductions in both weight and HbA1c, compared with 28% of those on placebo, according to Dr. Canovatchel.

Genital mycotic infections, urinary tract infections, and those related to osmotic diuresis were among the adverse events associated with canagliflozin, which was generally well tolerated, he said. The drug was associated with a low rate of hypoglycemia.

Canagliflozin (Invokana) was the first SGLT2 inhibitor to be approved in the United States, in March 2013. These agents, taken orally, work by inhibiting SGLT2 that is expressed in the kidney, reducing renal glucose reabsorption, increasing urinary excretion of glucose, and reducing plasma glucose levels.

The study was published last year (Diabetes Obes. Metab. 2013;15:372-82).

Dr. Canovatchel is an employee of Janssen, the manufacturer of canagliflozin.

emechcatie@frontlinemedcom.com

Recommended Reading

Diabetes prevalence increases, but so does diabetes control
MDedge Endocrinology
FDA approves GLP-1 receptor agonist albiglutide for type 2 diabetes
MDedge Endocrinology
Complication rates decline among diabetes patients
MDedge Endocrinology
Asymptomatic stenosis could cause cognitive impairment
MDedge Endocrinology
Better blood pressure, glycemic control in patients with type 2 diabetes on CPAP for apnea
MDedge Endocrinology
LDL particle number advantageous in managing cardiovascular risk
MDedge Endocrinology
High animal protein intake linked to later diabetes
MDedge Endocrinology
Adding empagliflozin to metformin improved glycemic control in type 2 diabetes
MDedge Endocrinology
RM-131 makes headway against diabetic gastroparesis
MDedge Endocrinology
Walking disability raises red flag in diabetics with OA
MDedge Endocrinology