16 November 2021 - - US-based biotechnology company Moderna, Inc. (NASDAQ: MRNA) has released positive data from the AstraZeneca-led Phase 2 (EPICCURE) study evaluating the use of an mRNA therapeutic that encodes for vascular endothelial growth factor-A (VEGF-A) (AZD8601) in patients undergoing coronary artery bypass grafting, the company said.

These data were presented TODAY at the American Heart Association's Scientific Sessions 2021 annual meeting.

The Phase 2 study met the primary endpoint of safety and tolerability of AZD8601. In the study of 11 patients, seven were treated with AZD8601 VEGF-A mRNA and four received placebo injections.

Numerical trends were observed in endpoints in the heart failure efficacy domains compared with placebo, including increase in left ventricular ejection fraction and patient reported outcomes.

In addition, all seven patients treated with AZD8601 had NT-proBNP levels below heart failure limit at six months follow-up compared to one of four patients treated with placebo.

AZD8601 is an investigational, locally administered mRNA therapy that encodes for VEGF-A.

EPICCURE is a randomized, placebo-controlled, double-blind, multicenter, six-month, Phase 2a clinical trial of the safety, tolerability, and exploratory efficacy of epicardial injections of AZD8601 in patients with stable coronary artery disease and moderately decreased LVEF who are undergoing CABG surgery.

Exploratory efficacy endpoints included left ventricular ejection fraction, NT-proBNP (a biomarker which measures the level of a hormone which is elevated in patients with heart failure), and functional patient reported outcomes.

Coronary artery disease is caused by blockages in the main coronary arteries and resulting insufficient blood flow to the myocardium is the primary cause of ischemic heart failure. More than 18.2m adults older than 20 years of age in the US have coronary disease.

And two in ten deaths from coronary disease happen in adults younger than 65 years of age.

Coronary disease can lead to myocardial infarction, which can lead to heart failure.

Additionally, chronic coronary artery disease, even without heart attack, can lead to inadequate blood supply to part of the heart and cause the muscle to not pump effectively, leading to heart failure.

Heart failure affects approximately 40 m adults globally and it is estimated that the prevalence will increase by 46% in the next decade.

The prognosis of heart failure remains poor, with mortality estimated at approximately 25-50% in patients at only five years from diagnosis.

Heart failure is also a burden on the healthcare system, representing 2% to 3% of national health expenditures in high-income countries, which is projected to double in the next 20 years.

The Phase 2 study of AZD8601 is being conducted by AstraZeneca and is evaluating safety and tolerability in patients with chronic heart failure.

Patients undergoing coronary artery bypass surgery with reduced left ventricular ejection fraction were randomized to a series of epicardial injections in ischemic but viable myocardium at the time of surgery with AZD8601 or placebo.

Study endpoints include safety and tolerability, as well as exploratory efficacy endpoints including coronary blood flow, left ventricular function, wall motion and overall cardiac function.

Clinical symptoms were evaluated through established quality of life questionnaires as well as biomarkers including NT-proBNP, markers known to be associated with cardiac prognosis. Patients were followed for six months.

In an established porcine model of myocardial infarction, a single epicardial administration of VEGF mRNA (AZD8601) ten days after induced myocardial infarction improved left ventricular ejection fraction at 2 months compared to placebo.

In addition, infarct size was significantly reduced. These and other preclinical data supported advancement into clinical trials.

The Phase 1 study of AZD8601 evaluated safety and angiogenic potential in men with Type 2 diabetes.

Participants received intradermal injections of AZD8601 or placebo at randomized sites on their forearm, acting as their own controls.

Intradermal VEGF-A mRNA was well tolerated and led to local functional VEGF-A protein expression 24 hours after administration as well as transient local enhancement of basal skin blood flow at four hours and seven days after administration.

The results supported the suggestion that AZD8601 has the potential for regenerative angiogenesis.