Now that AstraZeneca PLC’s diabetes drug Farxiga has got a game-changing approval for heart failure in the US, the company believes indication-based pricing makes sense for the SGLT2 inhibitor given its potential for keeping thousands of patients out of hospital.
The US Food and Drug Administration approved Farxiga (dapagliflozin) to reduce the risk of cardiovascular death and hospitalization in adults with heart failure with reduced ejection fraction (HFrEF) regardless of whether they have type 2 diabetes or not. The approval, which was issued late on 5 May and followed a priority review that was only granted by the agency in January this year, was based on stellar results from the landmark Phase III DAPA-HF trial
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