AZ TO PRESENT NEW DATA AT ADA


ASTRAZENECA TO PRESENT NEW DATA FROM ITS BROAD PORTFOLIO IN WIDE RANGE OF
PATIENT POPULATIONS AT THE AMERICAN DIABETES ASSOCIATION 74TH SCIENTIFIC
SESSIONS®

43 abstracts on approved products and an investigational compound accepted for
presentation

First data from Phase III trial of saxagliptin/dapagliflozin combination
presented as a late-breaker

First six-year, open-extension to the DURATION-1 trial examining the efficacy
and tolerability of exenatide will be presented

AstraZeneca today announced that 43 abstracts reporting results of the company's
research and development in diabetes have been accepted for presentation at the
74th Scientific Sessions® of the American Diabetes Association (ADA) in San
Francisco, 13-17 June 2014. Clinical data from studies evaluating multiple
approved products, including Forxiga® (dapagliflozin, marketed in the US as
Farxiga™), Bydureon® (exenatide extended-release for injectable suspension) and
Onglyza® (saxagliptin), as well as the investigational combination of
saxagliptin and dapagliflozin, demonstrate AstraZeneca's continued commitment to
addressing unmet medical needs across a wide spectrum of type 2 diabetes
patients in different stages of the disease.

Pascal Soriot, Chief Executive Officer, AstraZeneca, said: "The robust
scientific data that will be presented at ADA further strengthen our broad
innovative portfolio that spans the entire spectrum of non-insulin anti-diabetic
treatments. Our continued focus on advancing scientific knowledge reinforces our
long-term commitment to diabetes, a core strategic area for us and an important
platform for returning AstraZeneca to growth."

"Diabetes is a progressive and complex disease which demands combination
approaches to further improve patient care," said Briggs Morrison, MD, Executive
Vice President, Global Medicines Development & Chief Medical Officer,
AstraZeneca. "Our data accepted for presentation at this year's ADA, including
trials evaluating our medicines in patients with significant comorbidities and
in combination with other anti-diabetic agents, reflect AstraZeneca's efforts to
provide these treatment options that address the needs of patients at different
stages of the disease."

Notable data on an AstraZeneca investigational compound at ADA include:

  · A late-breaker of the first presentation of Phase III data evaluating the
investigational combination of saxagliptin/dapagliflozin as a dual add-on
therapy in adult patients with type 2 diabetes who were inadequately controlled
on metformin,  the top-line results of which were announced in
May (http://www.astrazeneca.com/Media/Press-releases/Article/20140513-
-astrazeneca-announces-positive-results-from-phase-iii-saxagliptin-dapagliflozin
-combination). Results being presented at ADA, and published in the abstract
available in Diabetes, include secondary outcome measures on body weight and
efficacy. (#127-LB, Sunday, 15 June, 12:00 PM PDT)[i] (http://about:blank#_edn1)

Notable data on approved AstraZeneca products at ADA include:

  · An analysis from nine double-blind, placebo-controlled trials evaluating the
safety of dapagliflozin in elderly patients (#269-OR, Monday, 16 June, 9:30 AM
PDT)[ii] (http://about:blank#_edn2)
  · An analysis from three randomised controlled trials examining the effect of
exenatide extended-release for injectable suspension on daily blood glucose
variability compared with basal insulin (#997-P, Saturday, 14 June, 11:30 AM
PDT)[iii] (http://about:blank#_edn3)
  · A sub-group analysis from the SAVOR trial examining the effect of
saxagliptin on renal outcomes (#544-P, Saturday, 14 June, 11:30 AM
PDT)[iv] (http://about:blank#_edn4)
  · An analysis from two double-blind, placebo-controlled trials evaluating the
effects of dapagliflozin on systolic blood pressure (#1033-P, Sunday, 15 June,
12:00 PM PDT)[v] (http://about:blank#_edn5)
  · A sub-group analysis from the SAVOR trial examining the effect of
saxagliptin in elderly patients from the study population (#1057-P, Sunday, 15
June, 12:00 PM PDT)[vi] (http://about:blank#_edn6)
  · An open-ended extension to the DURATION-1 trial examining the efficacy and
tolerability of exenatide once-weekly over six years (#964-P, Saturday, 14 June,
11:30 AM PDT)[vii] (http://about:blank#_edn7)
  · An analysis from five placebo-controlled trials examining the effects of
saxagliptin on β-cell function in patients with latent autoimmune diabetes (#152
-OR, Sunday, 15 June, 8:45 AM PDT)[viii] (http://about:blank#_edn8)

The complete list of AstraZeneca data presentations can be accessed on the ADA
website here (http://www.abstractsonline.com/plan/start.aspx?mkey=%7b40FC5C61
-819A-4D1B-AABA-3705F7D0EA76%7d).

CONTACTS

Media Enquiries
Esra Erkal-Paler                          +44 20 7604 8030 (UK/Global)
Vanessa Rhodes                         +44 20 7604 8037 (UK/Global)
Ayesha Bharmal                          +44 20 7604 8034 (UK/Global)
Jacob Lund                                  +46 8 553 260 20 (Sweden)
Michele Meixell                            + 1 302 885 6351 (US)

Investor Enquiries
Karl Hård                                     +44 20 7604 8123  mob: +44 7789
654364
Colleen Proctor                            + 1 302 886 1842     mob:  +1 302 357
4882
Anthony Brown                            +44 20 7604 8067     mob: +44 7585
404943
Jens Lindberg                              +44 20 7604 8414     mob: +44 7557
319729

----------------------------------------------------------------------

[i] (http://about:blank#_ednref1) Rosenstock, J., et al. "Dual Add-On Therapy in
Poorly Controlled Type 2 Diabetes on Metformin: Randomized, Double-Blind Trial
of Saxagliptin+Dapagliflozin vs Saxagliptin and Dapagliflozin Alone." American
Diabetes Association Scientific Sessions 2014. Abstract #127-LB.

[ii] (http://about:blank#_ednref2) Mansfield, T., et al. "Dapagliflozin is Safe
and Well-tolerated in Older patients with T2DM." American Diabetes Association
Scientific Sessions 2014. Abstract #269-OR.

[iii] (http://about:blank#_ednref3) Vora, J., et al. "Daily Blood Glucose
Variability With Exenatide Once-Weekly Vs Basal Insulin in 3 RCTs." American
Diabetes Association Scientific Sessions 2014. Abstract #997-P.

[iv] (http://about:blank#_ednref4) Mosenzon, O., et al. "Effect of Saxagliptin
on Renal Outcomes." American Diabetes Association Scientific Sessions 2014.
Abstract #544-P.

[v] (http://about:blank#_ednref5) Weber, M., et al. "Dapagliflozin Lowered
Ambulatory Blood Pressure in Patients With T2DM and Hypertension Inadequately
Controlled by a Renin-Angiotensin System Blocker With or Without Another Agent."
American Diabetes Association Scientific Sessions 2014. Abstract #1033-P.

[vi] (http://about:blank#_ednref6) Leiter, L., et al. "Efficacy and Safety of
Saxagliptin in Older Participants in the SAVOR-TIMI 53 Trial." American Diabetes
Association Scientific Sessions 2014. Abstract #1057-P.

[vii] (http://about:blank#_ednref7) Henry, R., et al. "An open-ended extension
to the DURATION-1 trial examining the efficacy and tolerability of exenatide
once-weekly over six years." American Diabetes Association Scientific Sessions
2014. Abstract #964-P.

[viii] (http://about:blank#_ednref8) Pozzilli P., et al. "Saxagliptin Increases
β-Cell Function and Improves HOMA Index in Patients with Latent Autoimmune
Diabetes in Adults." American Diabetes Association Scientific Sessions 2014.
Abstract #152-OR.



11 June 2014

-ENDS-
GlobeNewswire