Less Ads, More Data, More Tools Register for FREE

Pin to quick picksAstrazeneca Regulatory News (AZN)

Share Price Information for Astrazeneca (AZN)

Share Price is delayed by 15 minutes
Get Live Data
13,234.00    80.00 (0.61%)
Bid:
13,216.00
Ask:
13,220.00
Spread: 4.00 (0.03%)
Market Cap: £205.24b
AZN Live PriceLast checked at - London Stock Exchange

Intraday Astrazeneca Share Chart

Bydureon EXSCEL trial meets T2D safety objective

23 May 2017 07:00

RNS Number : 9298F
AstraZeneca PLC
23 May 2017
 

This announcement contains inside information

 

23 May 2017 07:00 BST

 

BYDUREON EXSCEL TRIAL MEETS PRIMARY SAFETY OBJECTIVE IN TYPE-2 DIABETES PATIENTS AT WIDE RANGE OF CARDIOVASCULAR RISK

 

Based on a composite measure of major adverse CV events (MACE), Bydureon did not increase cardiovascular (CV) risk and showed a consistent safety profile

 

Fewer CV events were observed in the Bydureon arm, however, the efficacy objective of reduction in CV risk did not reach statistical significance

 

AstraZeneca today announced top-line results from the Phase IIIb/IV EXSCEL (EXenatide Study of Cardiovascular Event Lowering) trial. The trial compared the effect of once-weekly Bydureon (exenatide extended-release) versus placebo, when added to usual type-2 diabetes care, on the risk of MACE, a composite endpoint of CV death, non-fatal myocardial infarction or non-fatal stroke, in adults with type-2 diabetes (T2D) at a wide range of CV risk.

 

The EXSCEL trial met its primary safety objective of non-inferiority for MACE. These results address the US Food and Drug Administration (FDA) requirement that medicines to treat T2D are not associated with an increase in CV risk. Fewer CV events were observed in the Bydureon arm of the trial, however, the efficacy objective of a superior reduction in MACE did not reach statistical significance. Data were consistent with the known safety profile of Bydureon.

 

Elisabeth Björk, Vice President, Head of Cardiovascular and Metabolic Diseases, Global Medicines Development, AstraZeneca, said: "These top-line results from the EXSCEL trial provide robust evidence of the cardiovascular safety profile of Bydureon across a wide range of patients with type-2 diabetes. Furthermore, the trial design and broad inclusion criteria of EXSCEL offer physicians relevant data applicable to clinical practice."

 

The EXSCEL trial is the largest and most inclusive patient population of any CV outcomes trial of the glucagon-like peptide-1 (GLP-1) receptor agonist class conducted to date, having included more than 14,000 patients from 35 countries.

 

A full evaluation of the EXSCEL data is ongoing. The results will be presented at the European Association for the Study of Diabetes (EASD) annual meeting on Thursday, 14 September 2017 in Lisbon, Portugal.

 

About EXSCEL

EXSCEL is a Phase IIIb/IV, double-blind, placebo-controlled, global CV outcomes trial conducted in 35 countries and enrolled more than 14,000 patients with type-2

diabetes with or without additional CV risk factors or prior CV events. Participants were randomised to receive exenatide once-weekly 2mg or matching placebo by subcutaneous injections. EXSCEL was run jointly by two academic research organisations - the Duke Clinical Research Institute (Durham, NC, US) and the University of Oxford Diabetes Trials Unit (Oxford, UK).

 

About AstraZeneca in Diabetes

AstraZeneca is pushing the boundaries of science with the goal of developing life-changing medicines that aim to reduce the global burden and complications of diabetes. As a main therapy area for the company, we are focusing our research and development efforts on diverse populations and patients with significant co-morbidities, such as cardiovascular disease, obesity, non-alcoholic steatohepatitis (NASH), and chronic kidney disease.

Our commitment to diabetes is exemplified by the depth and breadth of our global clinical research programme. This commitment is advancing understanding of the treatment effects of our diabetes medicines in broad patient populations, as well as exploring combination products to help more patients achieve treatment success earlier in their disease.

 

About AstraZeneca in Cardiovascular & Metabolic Diseases (CVMD)

Cardiovascular, renal and metabolic diseases are key areas of focus for AstraZeneca as part of the company's strategy for achieving scientific leadership and returning to growth. By collaborating across therapeutic disciplines within the CVMD therapy area, we are addressing the underlying disorders that drive CVMD risk, with the goal of reducing morbidity, mortality and organ damage through innovative therapies. Recognising the growing unmet needs and challenges faced by the millions of people worldwide living with these interrelated diseases, we are determined to understand how they interact and impact one another - and how they can be treated together to save more patients' lives.

 

About AstraZeneca

AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of diseases in three main therapy areas - Oncology, Cardiovascular & Metabolic Diseases and Respiratory. The Company also is selectively active in the areas of Autoimmunity, Neuroscience and Infection. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information, please visit www.astrazeneca.com and follow us on Twitter @AstraZeneca.

 

Media Enquiries

 

 

 

 

 

Esra Erkal-Paler

UK/Global

+44 203 749 5638

Karen Birmingham 

UK/Global 

+44 203 749 5634 

Rob Skelding 

UK/Global 

+44 203 749 5821 

Jacob Lund 

Sweden 

+46 8 553 260 20 

Michele Meixell 

US 

+1 302 885 2677 

 

 

 

Investor Relations

 

 

Thomas Kudsk Larsen

 

 

 

+44 203 749 5712

 

Craig Marks

 

Finance, Fixed Income, M&A

 

+44 7881 615 764

 

Henry Wheeler

 

Oncology

 

+44 203 749 5797

 

Mitchell Chan

 

Oncology

 

+1 240 477 3771

 

Lindsey Trickett

 

Cardiovascular & Metabolic Diseases

 

+1 240 543 7970

 

Nick Stone

 

Respiratory

 

+44 203 749 5716

 

Christer Gruvris

Autoimmunity, Neuroscience & Infection

+44 203 749 5711

US toll free

 

+1 866 381 7277

 

Adrian Kemp

Company Secretary, AstraZeneca PLC

This information is provided by RNS
The company news service from the London Stock Exchange
 
END
 
 
MSCSEUSIDFWSEFI
Date   Source Headline
15th Jun 20267:00 amRNSTruqap approved in US for prostate cancer
1st Jun 20263:05 pmRNSAdmission of Further Securities to Trading
1st Jun 20263:00 pmRNSTotal Voting Rights
29th May 20267:00 amRNSImfinzi approved in US for early bladder cancer
27th May 20267:00 amRNSUS FDA decision date on camizestrant extended
26th May 20267:00 amRNSEnhertu recommended in EU for HER2+ solid tumours
26th May 20267:00 amRNSCamizestrant recommended for breast cancer in EU
26th May 20267:00 amRNSDatroway approved in US for 1L triple-negative BC
18th May 20263:00 pmRNSDirector/PDMR Shareholding
18th May 20267:05 amRNSEnhertu approved in two HER2+ early BC settings
18th May 20267:00 amRNSBaxfendy approved in the US for hypertension
14th May 20267:00 amRNSImfinzi + EV improves EFS & OS in bladder cancer
1st May 20263:00 pmRNSTotal Voting Rights and Admission of Shares
1st May 20267:05 amRNSFDA ODAC vote on camizestrant in breast cancer
1st May 20267:00 amRNSFDA ODAC recommends Truqap in prostate cancer
29th Apr 20267:00 amRNS1st Quarter Results
28th Apr 20267:00 amRNSBreztri approved in the US for asthma
27th Apr 20267:00 amRNSSaphnelo self-administration approved in the US
23rd Apr 20267:00 amRNSDirectorate change
21st Apr 20267:00 amRNSI CAN PhIII interim analysis met primary endpoint
20th Apr 20267:00 amRNSThird tozorakimab positive Phase III in COPD
9th Apr 20265:15 pmRNSResult of AGM
2nd Apr 20267:00 amRNSImfinzi+Imjudo improves PFS in early liver cancer
1st Apr 20263:00 pmRNSTotal Voting Rights and Admission of Shares
31st Mar 20267:00 amRNSEfzimfotase alfa Ph3 program show positive results
27th Mar 20267:00 amRNSTozorakimab met OBERON/TITANIA primary endpoints
20th Mar 202611:00 amRNSNotification of Admission of Shares
16th Mar 20267:00 amRNSImfinzi approved in EU for early gastric cancer
16th Mar 20267:00 amRNSImfinzi approved in EU for early gastric cancer
10th Mar 202611:00 amRNSNotice of AGM
10th Mar 202611:00 amRNSNotice of AGM
6th Mar 202611:10 amRNSDirector/PDMR Shareholding
6th Mar 202611:05 amRNSDirector/PDMR Shareholding
6th Mar 202611:00 amRNSDirector/PDMR Shareholding
2nd Mar 20263:00 pmRNSTotal Voting Rights
26th Feb 20267:00 amRNSAstraZeneca prices a $2bn bond offering
25th Feb 20267:00 amRNSFiling of Form 20-F with SEC
24th Feb 202611:00 amRNSAnnual Financial Report
24th Feb 20267:00 amRNSDirectorate change
20th Feb 20267:00 amRNSFixed-duration Calquence combo approved in US
10th Feb 20267:00 amRNSFinal Results
3rd Feb 20267:00 amRNSUpdate on Saphnelo subcutaneous administration
2nd Feb 20263:00 pmRNSTotal Voting Rights
2nd Feb 20267:05 amRNSImfinzi recommended in EU for early gastric cancer
2nd Feb 20267:00 amRNSAstraZeneca begins trading on NYSE
30th Jan 20267:00 amRNSAstraZeneca agrees obesity and T2D deal with CSPC
29th Jan 20269:51 amRNSAstraZeneca invests $15bn in China through 2030
20th Jan 20267:00 amRNSAstraZeneca to complete direct listing on NYSE
8th Jan 20267:00 amRNSAZN new Head of Investor Relations Joris Silon
2nd Jan 20263:00 pmRNSTotal Voting Rights

Due to London Stock Exchange licensing terms, we stipulate that you must be a private investor. We apologise for the inconvenience.

To access our Live RNS you must confirm you are a private investor by using the button below.