AstraZeneca to present new cardiovascular data on Farxiga in type-2 diabetes at ACC 2019

Report this content

First sub-analyses from Phase III DECLARE-TIMI 58 trial selected for late-breaking clinical trial and oral presentations

Data evaluating the cardiovascular (CV) effects of Farxiga (dapagliflozin), including hospitalisation for heart failure (hHF) in adults with type-2 diabetes (T2D) have been selected for late-breaking clinical trial and oral presentations at the American College of Cardiology’s (ACC) 68th Annual Scientific Session on 16-18 March. The data are the first sub-analyses from the Phase III DECLARE-TIMI 58 trial for Farxiga.

AstraZeneca will also present the latest results from the Brilinta (ticagrelor) Phase III TREAT trial in patients with the most dangerous form of heart attack, ST-segment elevation myocardial infarction (STEMI), and a new heart failure analysis from CVD-REAL, the first large real-world evidence study of its kind evaluating the risk of all-cause death and hHF in patients with T2D receiving treatment with a SGLT2 inhibitor (SGLT2i), including Farxiga.

Joris Silon, Senior Vice President, Cardiovascular, Renal and Metabolism, BioPharmaceuticals, said: “AstraZeneca is committed to addressing some of the most pressing health problems faced by patients with cardiovascular and metabolic diseases, by identifying and mitigating specific risks. This is particularly important in reducing the prevalence and burden of heart failure. This disease affects nearly 64 million people globally, and is an early and frequent complication in patients with type-2 diabetes.”

AstraZeneca will present 21 abstracts at ACC 2019. Highlights include (all times are Central):

Farxiga Phase III DECLARE-TIMI 58

  • Dapagliflozin and Cardiovascular Outcomes in Patients With Type 2 Diabetes and Prior Myocardial Infarction: A Sub-Analysis From DECLARE TIMI-58 Trial (Oral Presentation: #906-04. Monday 18 March, 8:12– 8:22 AM, Room 211).
  • Effect of Dapagliflozin on Heart Failure and Mortality in Type 2 Diabetes Mellitus Based on Ejection Fraction (Late-Breaking Clinical Trial Presentation: #409-14. Monday 18 March, 8:45–8:55 AM, Main Tent, Great Hall).

Brilinta Phase III TREAT

TREAT was designed to evaluate the safety and efficacy of Brilinta compared with clopidogrel in patients who were diagnosed with STEMI treated with pharmacological thrombolysis.

  • Efficacy of Ticagrelor vs Clopidogrel After Fibrinolytic Therapy in Patients With ST-Elevation Myocardial Infarction (Late-Breaking Clinical Trial Presentation: #410-12. Monday 18 March, 11:15–11:25 AM, Main Tent, Great Hall).

Real-world evidence

New data on the increased and persistent risk of recurrent CV events in patients with CV disease and additional risk factors, and outcomes of patients with T2D with reduced or preserved ejection fraction.

  • Novel Approach to Quantifying Risk of Major Cardiovascular Events in Patients 1-3 Years PostMyocardial Infarction: Insights From the Global Prospective TIGRIS Registry (Poster Presentation: #1131-407. Saturday 16 March, 10:00–10:45 AM, Poster Hall, Hall F).
  • Use of Evidence-Based Preventive Medical Therapies 1-3 Years Post-Myocardial Infarction in the Prospective Global TIGRIS Registry (Poster Presentation: #1231-391. Sunday 17 March, 9:45–10:30 PM, Poster Hall, Hall F).
  • US Burden of Illness in a Commercially-Insured Population and Assessment of The High risk and unmEt Need in patients with CAD and type 2 diabetes (ATHENA): US Burden of Illness in the Diabetes Collaborative Registry (Poster Presentation: #1129-361 and #1129-362. Saturday 16 March, 10:00–10:45 PM, Poster Hall, Hall F).
  • Initiation of Sodium Glucose Cotransporter-2 Inhibitors Versus Other Glucose Lowering Drugs and Risk of Hospitalization For Heart Failure and Death in Patients With Type 2 Diabetes With Reduced and Preserved Left Ventricular Ejection Fraction (Moderated Poster Presentation: #1024-07. Sunday 17 March, 10:15–10:25 AM, Poster Hall, Hall F).

For a complete list of AstraZeneca data presentations at ACC 2019, please access the ACC website here.

-ENDS-

NOTES TO EDITORS

About AstraZeneca in Cardiovascular, Renal & Metabolism (CVRM)

Cardiovascular, renal and metabolic diseases together form one of AstraZeneca’s main therapy areas and a key growth driver for the Company. By following the science to understand more clearly the underlying links between the heart, kidney and pancreas, AstraZeneca is investing in a portfolio of medicines to protect organs and improve outcomes by slowing disease progression, reducing risks and tackling co-morbidities. Our ambition is to modify or halt the natural course of CVRM diseases and potentially regenerate organs and restore function, by continuing to deliver transformative science that improves treatment practices and cardiovascular health for millions of patients worldwide.

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 therapy areas - Oncology, Cardiovascular, Renal & Metabolism and Respiratory. 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 Relations
Gonzalo Viña UK/Global +44 203 749 5916
Rob Skelding UK/Global +44 203 749 5821
Matt Kent UK/Global +44 203 749 5906 
Jennifer Hursit UK/Global +44 203 749 5762
Christina Malmberg Hägerstrand Sweden +46 8 552 53 106 
Michele Meixell  US +1 302 885 2677
Investor Relations 
Thomas Kudsk Larsen +44 203 749 5712
Henry Wheeler Oncology +44 203 749 5797
Christer Gruvris BioPharma - Cardiovascular; Metabolism +44 203 749 5711
Nick Stone BioPharma - Respiratory; Renal +44 203 749 5716
Josie Afolabi Other +44 203 749 5631
Craig Marks Finance; Fixed Income +44 7881 615 764
Jennifer Kretzmann Retail Investors; Corporate Access +44 203 749 5824
US toll-free +1 866 381 72 77

Prenumerera