AstraZeneca's Forxiga Gets EC Approval For Type-I Diabetes

 | Mar 24, 2019 10:10PM ET

AstraZeneca plc (NYSE:AZN) announced that the European Commission (EC) has approved a label expansion of its diabetes drug, Forxiga (dapagliflozin).

Forxiga has been approved for the treatment of type-1 diabetes (T1D) as an adjunct to insulin in patients with a BMI ≥ 27 kg/m2 when insulin alone does not provide adequate glycemic control despite optimal insulin therapy.

The approval was based on encouraging data from the phase III DEPICT study for Forxiga in T1D. Short-term (24 week) and long-term (52 week) data from DEPICT-1 along with short-term data from DEPICT-2 showed that Forxiga 5mg daily resulted in significant and clinically-meaningful reductions from baseline in average blood glucose levels HbA1c (primary endpoint), weight and total daily insulin dose (secondary endpoints) at 24 and 52 weeks.

We remind investors that Forxiga, a first-in-class, oral once-daily selective inhibitor of human sodium-glucose co-transporter 2 (SGLT2), is already approved as both monotherapy and combination therapy to improve glycemic control, with additional benefits of weight loss and blood pressure reduction, as an adjunct to diet and exercise in adults with type-2 diabetes (T2D).

In the past year, AstraZeneca’s shares have rallied 26.7%, outperforming the industry ’s growth of 17.2%.