Novo Nordisk receives positive opinion on Levemir(TM) (insulin detemir) from EU committee


Following the positive opinion from CPMP, Novo Nordisk anticipates that the European Commission will issue marketing authorisation for Levemir(TM) in the European Union within the coming months. Subsequent to the marketing authorisation Novo Nordisk expects to launch Levemir(TM) in key European markets in the second half of 2004.
 
Levemir(TM) is a long-acting insulin analogue that provides more consistent day-to-day control of blood glucose levels compared to conventional insulin preparations1-6. Among the benefits for people with diabetes, it has been demonstrated that Levemir(TM) reduces fasting blood glucose and the risk of hypoglycaemia, especially at night-time1-5. In addition, studies have shown that people using Levemir(TM) do not experience the undesirable weight gain often associated with conventional insulin preparations1-5, 7.
 
The positive opinion by CPMP for Levemir(TM) does not change Novo Nordisk expectations for the financial results for 2004.
 
 
 
 
Novo Nordisk is a healthcare company and a world leader in diabetes care. The company has the broadest diabetes product portfolio in the industry, including the most advanced products within the area of insulin delivery systems. In addition, Novo Nordisk has a leading position within areas such as haemostasis management, growth hormone therapy and hormone replacement therapy. Novo Nordisk manufactures and markets pharmaceutical products and services that make a significant difference to patients, the medical profession and society. With headquarters in Denmark, Novo Nordisk employs approximately 18,800 full-time employees in 69 countries, and markets its products in 179 countries. Novo Nordisk's B shares are listed on the stock exchanges in Copenhagen and London. Its ADRs are listed on the New York Stock Exchange under the symbol 'NVO'. For more information, visit www.novonordisk.com.
 
 
 
 
For further information please contact:
Media:
Investors:
 
 
Outside North America:
Outside North America:
Mike Rulis
Peter Haahr
Tel (direct):
(+45) 4442 3573
Tel (direct):
(+45) 4442 1207
 
 
In North America:
In North America:
Susan T Jackson
Christian Kanstrup
Tel (direct):
(+1) 609 919 7776
Tel (direct):
(+1) 609 919 7937
 
 
 
 

Stock Exchange Announcement No 18 / 2003
 
 
 
References:
 
1 Home P, Bartley P, Landin-Olsson M et. al.  Insulin detemir offers superior glycaemic control compared to NPH insulin in people with type 1 diabetes.  Diabetes Care 2004;(In press)
 
2 Pieber T, Grill V, Kristensen A et. al.  Treatment with Insulin Detemir Allows Flexible Timing of Administration in Subjects with Type 1 Diabetes. Diabetologia 2003;46(Suppl.2):A7
 
3 Hermansen K, Fontaine P, Kukolja KK et al. Benefits of Insulin Analogues over Human Insulins: Lower HbA1c and less hypoglycaemia using insulin detemir and insulin aspart. Diabetologia (In press)
 
4 Russell-Jones D, BolinderJ, Simpson R et al.  Lower and more predictable fasting blood glucose and reduced risk of nocturnal hypoglycaemia with once daily insulin detemir vs. NPH in subjects with type 1 diabetes.  Diabetologia 2002; 45 (suppl. 2): A51.
 
5 De Leeuw I, Vague P, Selam JL, Skeie S, Elte JWF, Lang H, Draeger E.  Lower risk of nocturnal hypoglycaemia and favourable weight development in type 1 diabetic subjects after 12 months treatment with insulin detemir vs. NPH insulin. Diabetologia 2002; 45 (suppl. 2); A257.
 
6 Heise T, Nosek L, Draeger E, et. al. Lower within-subject variability of insulin detemir in comparison to NPH insulin and insulin glargine in subjects with type 1 diabetes.  Diabetes 2003; 52(Suppl 1): A121.
 
7 Haak T, Tiengo A, Waldhausl W, Draeger E. Treatment with Insulin Detemir is Associated with Predictable Fasting Blood Glucose Levels and Favorable Weight Development in Subjects with Type 2 Diabetes. Diabetes Care 2003, 52 (Suppl 1): A120.

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