
FDA Approves Semaglutide Injection for Cardiovascular Risk Reduction
The GLP-1 agonist now has indications for the reduction of MACE and the management of A1C in patients with type 2 diabetes.
The US Food and Drug Administration (FDA) has approved a new indication for semaglutide (Ozempic) injection 0.5 mg or 1 mg for the reduction of
The indication is based on the results of the SUSTAIN 6 cardiovascular outcomes trials which examined the GLP-1 agonist’s safety when added to standard of care in adults with T2D and cardiovascular disease, versus placebo.
The Novo Nordisk drug was shown to significantly reduce the risk of a three-component MACE endpoint occurrence which included cardiovascular death, non-fatal heart attack, or non-fatal stroke. Over a median 2.1 years, patients treated with semaglutide reported a MACE relative risk reduction of 26% versus placebo (HR, .74; 95% CI, 0.58-0.95; P <.001).
The primary composite outcome occurred in just 6.6% of patients treated with the GLP-1 agonist plus standard of care, versus 8.9% of patients on placebo.
Gastrointestinal adverse events were more frequently reported among treated patients in the SUSTAIN 6 trial, the majority of which occurred in the first 30 weeks of treatment.
The FDA also announced the addition of Prescribing Information details to the label of oral semaglutide tablets (Rybelsus) 7 mg or 14 mg, regarding the primary analysis for PIONEER 6, showing the hazard ratio for time to first three-component MACE (HR, .79; 95% CI, 0.57-1.11).
The oral form of the therapy was originally approved for the improvement of glucose in patients with T2D unable to achieve A1C goals with current antidiabetic therapy
Regarding the Ozempic approval, Todd Hobbs, vice president and US chief medical officer of Novo Nordisk said the indication establishes the therapy as an option for the 2 critical aspects of T2D management: blood sugar control and cardiovascular risk reduction.
"There is a well-established link between cardiovascular disease and type 2 diabetes,” Hobbs said in a











































































