FDA Approves Wegovy Weight-Loss Drug to Lower Heart Disease Risks

Wegovy: FDA Approves Weight-Loss Drug to Reduce Cardiovascular Risk

Wegovy: FDA Approves Weight-Loss Drug to Reduce Cardiovascular Risk


The U.S. Food and Drug Administration has granted approval for Wegovy, a weight-loss drug, as a way to decrease cardiovascular risk in overweight adults. This milestone approval marks a significant expansion of the drug’s market potential.

Wegovy Overview

Wegovy, containing the same active ingredient as the popular diabetes drug Ozempic, initially received FDA approval for treating obese or overweight patients. Its success has made it a cultural sensation and a revenue-generating blockbuster for Novo Nordisk, the manufacturer.

Expert Statements

According to John Sharretts, M.D., from the FDA’s Center for Drug Evaluation and Research, Wegovy is the first weight loss medication to be approved for preventing cardiovascular events in adults with obesity or overweight and cardiovascular disease. Similarly, Novo Nordisk’s executive vice president, Martin Holst Lange, expressed satisfaction in Wegovy being the first therapy in the U.S. to help individuals manage weight and reduce cardiovascular risks.

Clinical Trial Results

A pivotal clinical trial conducted last year demonstrated a significant reduction in heart problems risk for overweight individuals using Wegovy. The high demand for the drug has caused supply shortages, prompting Novo Nordisk to implement aggressive production measures, including acquiring a contract manufacturer.


This is a developing story and will be updated as more information becomes available.

Read More of this Story at www.washingtonpost.com – 2024-03-08 22:26:00

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