Country for PR: United Kingdom
Contributor: PR Newswire Europe
Tuesday, September 17 2019 - 23:09
AsiaNet
Oral semaglutide improves glycaemic control in people with type 2 diabetes across baseline blood sugar levels
BARCELONA, Spain, Sept. 17, 2019, /PRNewswire-AsiaNet/ --

Novo Nordisk today announced findings from an exploratory analysis of the 
PIONEER trial programme, showing oral semaglutide (3, 7 and 14 mg) improved 
glycaemic control in people with type 2 diabetes across baseline HbA1c levels. 
Greater reductions in HbA1c were demonstrated with 7 mg and 14 mg oral 
semaglutide vs all comparators including placebo, Jardiance® (empagliflozin 25 
mg), Januvia® (sitagliptin 100 mg) or Victoza® (liraglutide 1.8 mg). The 
results were presented today at the 55th Annual Meeting of the European 
Association for the Study of Diabetes (EASD)[1]. Oral semaglutide is an 
investigational once-daily glucagon-like peptide-1 (GLP-1) analogue in a pill.

In the analysis, data from 5,657 participants in PIONEER 1–5, 7 and 8 were 
grouped by trial according to baseline HbA1c (less than or equal to 8.0%, 
greater than 8.0 – less than or equal to 9.0% and greater than 9.0%). The 
proportion of people with type 2 diabetes achieving an HbA1c target of less 
than 7% was greater with oral semaglutide 7 and 14 mg vs comparators in all 
trials and across all HbA1c baseline subgroups. 

"People with type 2 diabetes have individual treatment goals related to 
glycaemic control," said Dr Juris Meier, professor of medicine and head of the 
division of diabetology and GI endocrinology at the St. Josef-Hospital of the 
Ruhr-University of Bochum, Germany. "The findings from this analysis are 
particularly meaningful as they show that oral semaglutide improves glycaemic 
control in a wide spectrum of people with type 2 diabetes." 

The safety profile of oral semaglutide across the PIONEER programme was 
consistent with that of the GLP-1 receptor agonist class and similar to those 
seen with subcutaneous semaglutide.

"This analysis reinforces the findings seen throughout the PIONEER trial 
programme, demonstrating oral semaglutide's efficacy in HbA1c reductions 
compared to commonly used type 2 diabetes treatments," said Mads Krogsgaard 
Thomsen, executive vice president and chief science officer of Novo Nordisk. 
"If approved, oral semaglutide will become the first and only oral GLP-1 
receptor agonist with the potential to help people with uncontrolled type 2 
diabetes better manage their condition." 

About the exploratory analysis and the PIONEER clinical trial programme

The PIONEER 1-5, 7 and 8 trials, included in this analysis, investigated oral 
semaglutide against diet and exercise (PIONEER 1), empagliflozin 25 mg (PIONEER 
2), sitagliptin 100 mg (PIONEER 3 and 7), liraglutide 1.8 mg (PIONEER 4) and as 
an add-on to insulin (PIONEER 8). PIONEER 5 evaluated oral semaglutide compared 
to placebo in patients with moderate renal impairment. 

The PIONEER phase 3a clinical development programme for oral semaglutide was a 
global development programme that enrolled 9,543 people with type 2 diabetes 
across 10 clinical trials. 

Novo Nordisk is a global healthcare company with more than 95 years of 
innovation and leadership in diabetes care. This heritage has given us 
experience and capabilities that also enable us to help people defeat obesity, 
haemophilia, growth disorders and other serious chronic diseases. Headquartered 
in Denmark, Novo Nordisk employs approximately 41,600 people in 80 countries 
and markets its products in more than 170 countries. For more information, 
visit novonordisk.com, Facebook (https://www.facebook.com/novonordisk), Twitter 
(https://twitter.com/novonordisk), LinkedIn 
(https://www.linkedin.com/company/novo-nordisk), 
YouTube(https://www.youtube.com/user/novonordisk/custom?app=desktop). 

References
1. Meier JJ, Bauer R, Blicher TM, et al. Efficacy of oral semaglutide according 
to baseline HbA1c: an exploratory subgroup analysis of the PIONEER trial 
programme. 55th Annual Meeting of the European Association for the Study of 
Diabetes. Barcelona, September 2019. 

Further information:

Media: 
Mette Kruse Danielsen: +45 3079 3883, mkd@novonordisk.com  
Ken Inchausti (US): +1 609 240 9429, kiau@novonordisk.com 

Investors: 
Peter Hugreffe Ankersen: +45 3075 9085, phak@novonordisk.com  
Valdemar Borum Svarrer: +45 3079 0301, jvls@novonordisk.com  
Ann Søndermølle Rendbæk: +45 3075 2253, arnd@novonordisk.com  
Kristoffer Due Berg (US): +1 609 235 2989, krdb@novonordisk.com  

Source: Novo Nordisk