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Early identification and treatment can reduce the chance of permanent joint damage and the number and severity of attacks

Reducing this risk is a key part of our commitment to driving change for this community, as we work to increase manufacturing capacity to responsibly supply this important medicine. The FDA decision is based on the results of the landmark SELECT phase 3 cardiovascular outcomes trial that examined the effect of adding Wegovy 2.4 mg or placebo to cardiovascular standard of care in adults with overweight and obesity with established CVD and without diabetes

Supplied as a sterile lyophilised powder in 20mg, 30mg and 40mg vials, each batch is verified to 98% purity by RP-HPLC and mass spectrometry

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