New Phase 3a findings show IDegLira, the investigational once-daily single injection combination of insulin degludec and liraglutide, for the treatment of people with type 2 diabetes, maintained its glucose-lowering effect and confirmed safety evaluations for up to one year.1 Findings from the 26-week extension of the DUALTM I clinical trial programme were presented at the 74th Annual Scientific Sessions of the American Diabetes Association (ADA) in San Francisco, CA.
The DUALTM I extension trial compared the efficacy and safety of IDegLira with insulin degludec and liraglutide 1.8 mg alone in insulin-naïve adults with type 2 diabetes uncontrolled on metformin with or without pioglitazone. At 52 weeks, IDegLira demonstrated a statistically significant and sustained HbA1c (blood glucose) reduction of 1.8% from baseline versus 1.4% for insulin degludec and 1.2% for liraglutide (p1
"Maintaining glycaemic control as diabetes progresses is an ongoing problem as patients fear initiating new therapies that may increase the risk of side effects such as weight gain and hypoglycaemia," said Professor John Buse, University of North Carolina School of Medicine, Chapel Hill, North Carolina, U.S. "All of the IDegLira data presented here at ADA indicate that this treatment can address these patient concerns."
At the end of the trial, the IDegLira treatment group observed a mean weight reduction of 0.4 kg (0.9 lbs), which was consistent with the first 26 weeks of treatment. Patients taking insulin degludec had a weight gain of 2.3 kg (5.1 lbs) and patients on liraglutide had a weight reduction of 3.0 kg (6.6 lbs). The estimated treatment difference between IDegLira and insulin degludec was -2.8 kg (-6.1 lbs) and the relative treatment difference between IDegLira and liraglutide was 2.7 kg (5.9 lbs).1
The daily insulin dose for patients on IDegLira remained stable throughout the extension phase (39 units) compared with insulin degludec (62 units). Patients treated with IDegLira had a 37% lower rate of hypoglycaemia versus insulin degludec (p1
Also during the scientific meeting, additional findings from two analyses based on the 52- week DUALTM I and 26-week DUALTM II trials were presented:
1. Impact of BMI on HbA1c Reduction, Hypoglycemia Rates and Insulin Requirements in Response to IDegLira in Patients With Type 2 Diabetes (Abstract #0066-OR; presented by John Buse)2
2. IDegLira Efficacy Across the Range of Disease Progression in Type 2 Diabetes (Abstract #0067-OR; presented by Helena Rodbard)3
The most frequently occurring adverse events (≥5%) seen at the conclusion of the DUALTM I extension trial for IDegLira, insulin degludec and liraglutide were diarrhoea (10.2%, 6.8%, 16.3%); nausea (10.3%, 3.9%, 22.3%); vomiting (5%, 2.4%, 9.2%); headache (12.8%, 10.9%, 14.6%); nasopharyngitis, usually referred to as the common cold (13.9%, 12.6%, 13.3%); increased lipase (5.8%, 4.4%, 8.5%); and decreased appetite (2.7%, 0.5%, 7.3%), respectively.4
About the DUALTM clinical programme
DUALTM (DUal Action of Liraglutide and Insulin Degludec in Type 2 Diabetes) consists of two phase 3a trials encompassing more than 2,000 people with type 2 diabetes.
DUALTM I (1,663 people) - a 26-week, randomised, parallel, three-arm, open-label, multicentre, trial conducted at 271 sites across 19 countries. The trial compared the efficacy and safety of IDegLira versus insulin degludec and liraglutide alone, in insulin- naïve adults with type 2 diabetes uncontrolled with metformin with or without pioglitazone. A 26-week extension phase of the main trial was conducted to generate longer-term safety and efficacy data. The topline results from the main period were reported in 2012.
DUALTM II (398 people) - a 26-week, randomised, parallel, two-arm, double-blinded, multicentre, trial conducted at 75 sites across seven countries. The trial compared the efficacy and safety of IDegLira and insulin degludec once daily, both added on to metformin in adults with type 2 diabetes uncontrolled on basal insulin (20-40 units) in combination with metformin with or without sulfonylurea/glinides. Sulfonylureas and glinides were discontinued at randomisation. In this trial, the allowed maximum dose of insulin degludec in the treatment arms was 50 units so as to be able to demonstrate the contribution of the liraglutide component of IDegLira on glycaemic control. The topline results were reported in 2012.
IDegLira, which is being developed for the treatment of type 2 diabetes, is a combination of insulin degludec, a once-daily basal insulin analogue with an ultralong duration of action, and liraglutide, a once-daily human GLP-1 analogue for the treatment of type 2 diabetes. IDegLira is being investigated in the Phase 3 DUALTM clinical trial programme. Novo Nordisk submitted the regulatory filing for IDegLira in the EU on 31 May 2013.
Insulin degludec has received regulatory approval and is marketed as Tresiba® in many countries including Argentina, Aruba, Bangladesh, Brazil, Chile, El Salvador, the EU, Iceland, India, Japan, Lebanon, Liechtenstein, Macedonia, Mexico, Norway, Russia and Switzerland. Insulin degludec is currently under review by the U.S. Food and Drug Administration.
About Victoza® (liraglutide [rDNA origin] injection)
Victoza® is a human glucagon-like peptide-1 (GLP-1) analogue that was approved by the U.S. Food and Drug Administration on January 25, 2010, as an adjunct to diet and exercise to improve blood sugar control in adults with type 2 diabetes.
As of January 2014, Victoza® has been commercially launched in 68 countries globally including the U.S., Canada, Japan, U.K., Germany, France, Italy, Denmark, Hungary, Russia, India, Brazil, Mexico, Argentina, Malaysia and China as well as a number of other countries, and will be available in other markets throughout 2014.