UNITED STATES
                       SECURITIES AND EXCHANGE COMMISSION
                             Washington, D.C. 20549

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                                    FORM 6-K

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                            REPORT OF FOREIGN ISSUER

                       Pursuant to Rule 13a-16 or 15d-16
                     of the Securities Exchange Act of 1934


                                  June 29, 2009


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                                NOVO NORDISK A/S
             (Exact name of Registrant as specified in its charter)


                                    NOVO ALLE
                               DK-2880, BAGSVAERD
                                     DENMARK
                    (Address of principal executive offices)

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Indicate by check mark whether the registrant files or will file annual reports
under cover of Form 20-F or Form 40-F

                       Form 20-F [X]     Form 40-F [ ]


Indicate by check mark whether the registrant by furnishing the information
contained in this Form is also thereby furnishing the information to the
Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934.

                             Yes [ ]     No [X]


If "Yes" is marked, indicate below the file number assigned to the registrant in
connection with Rule 12g-32(b):82-_____________________



RESEARCH UPDATE

NOVO NORDISK INSULIN ANALOGUES HAVE PROVEN SAFETY PROFILES

On Friday 26 June, Diabetologia, the journal of the European Association for the
Study of Diabetes (EASD) published online data from four studies relating to a
possible link between a long-acting insulin analogue, insulin glargine, and
cancer1. As a basis for such a possible link, an accompanying editorial explains
that certain insulin analogues have a structure making them more likely to bind
to the IGF-1 receptor which is known to be involved in promoting tumour growth2.

Novo Nordisk markets three insulin analogues, Levemir(R) (insulin detemir), a
long-acting basal insulin analogue, NovoRapid(R)/NovoLog(R) (insulin aspart), a
short-acting insulin analogue, and NovoMix(R)/NovoLog(R) Mix 70/30 (biphasic
insulin aspart). To avoid unnecessary speculation about whether Novo Nordisk
insulin analogues may be associated with an increased risk of cancer, the
company wishes to highlight the following:

o    For the past 20 years, all Novo Nordisk insulin analogues have been tested
     for IGF-1 receptor binding in the early research phase and only insulins
     with a binding ratio between the insulin and IGF-1 receptors similar to, or
     better than, that of human insulin have been accepted for further
     development3.

o    Studies on receptor binding and cell growth together show that insulin
     aspart, the insulin analogue present in NovoRapid(R)/NovoLog(R) and
     NovoMix(R)/NovoLog(R) Mix 70/30 has an in vitro safety profile that is
     identical to that of human insulin3,4.

o    Studies on receptor binding have shown that Levemir(R) in comparison to
     human insulin has a relative affinity to the IGF-1 receptor which is equal
     to or slightly lower than to the insulin receptor.4,5. Levemir(R)
     distinguishes itself from insulin glargine, which has been shown to have
     increased affinity for the IGF-1 receptor compared to human insulin4,5,6 .

o    All Novo Nordisk insulin analogues on the market have been studied in many
     randomised, controlled trials, in observational studies and are furthermore
     monitored for any safety signals through rigorous post-marketing safety
     surveillance. Novo Nordisk has not identified any cancer signals for any of
     the three insulin analogues.

o    Novo Nordisk has over the last 20 years discovered and developed insulin
     analogues to improve the treatment success rate for people with diabetes.
     Extensive clinical testing has provided evidence that Levemir(R),
     NovoRapid(R)/NovoLog(R) and NovoMix(R)/NovoLog(R) Mix 70/30 possess
     clinical advantages for many patients with diabetes compared to human
     insulin.

Mads Krogsgaard Thomsen, executive vice president and chief science officer of
Novo Nordisk, says: "Our science-driven approach to the discovery and
development of safe, improved insulin analogues, together with the existence of
comprehensive insulin safety databases, convinces us that our insulin analogues
improve treatment outcomes in diabetes patients relative to human insulin."

CONFERENCE CALL

On 29 June at 8 am CET, corresponding to 2 am EDT, a conference call for
investors will be held. Investors will be able to listen in via a link on the
investor section of novonordisk.com. Presentation material for the conference
call will be made available approximately one hour before on the same page.

ABOUT INSULIN AND IGF-1 RECEPTORS

Insulin can bind to two different receptors: insulin and IGF-1 (insulin-like
growth factor-1) receptors. The former mainly causes glucose lowering whereas
the latter mainly induces cell proliferation. Insulin binds much stronger (more
than 500-fold) to the insulin receptor than to the IGF-1 receptor and it is if
this binding profile is unfavourably changed due to alterations in the insulin
molecule that an insulin analogue can increase the risk of cell proliferation
via the IGF-1 receptor.


Novo Nordisk is a healthcare company and a world leader in diabetes care. 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 more than 27,900 employees in 81
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 novonordisk.com.

CONTACTS FOR FURTHER INFORMATION

Media:                           Investors:

Mike Rulis                       Mads Veggerby Lausten
Tel: (+45) 4442 3573             Tel: (+45) 4443 7919
mike@novonordisk.com             mlau@novonordisk.com

                                 Kasper Roseeuw Poulsen
                                 Tel: (+45) 4442 4471
                                 krop@novonordisk.com

In North America:                In North America:
Sean Clements                    Hans Rommer
Tel: (+1 609-514-8316            Tel: (+1) 609 919 7937
secl@novonordisk.com             hrmm@novonordisk.com

References:
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1 www.diabetologia-journal.org/
2 Baserga R, Peruzzi F, Reiss K (2003): The IGF-1 receptor in cancer biology.
Int J Cancer 107: 873-877
3 Gammeltoft S, Hansen BF, Dideriksen L, Lindholm A, Schaffer L, Trub T, Dayan
A, Kurtzhals P (1999): Insulin aspart, a novel rapid-acting human insulin
analogue. Exp Opin Invest Drugs 8 (9): 1431-1442
4 Kurtzhals P, Schaffer L, Sorensen A, Kristensen C, Jonassen I, Schmid C,
Trub T (2000): Correlations of receptor binding and metabolic and mitogenic
potenticies of insulin analogs designed for clinical use. Diabetes 49: 999-1005
5 Center for Drug Evaluation and Research, FDA. Application number 21-536:
Pharmacology review of insulin detemir
6 Shukla A, Grisouard J, Ehemann V, Hermani A, Ensmann H, Mayer D (2009)
Analysis of signalling pathways related to cell proliferation stimulated by
insulin analogs in human mammary epithelial cell lines. Endocrine-Related Cancer
16: 429-441

Company Announcement no 36 / 2009



                                   SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the
Registrant  has duly  caused  this  report  to be  signed  on its  behalf of the
undersigned, thereunto duly authorized.

Date: June 29, 2009                          NOVO NORDISK A/S
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                                            Lars Rebien Sorensen,
                                     President and Chief Executive Officer