Boehringer Ingelheim and Eli Lilly’s Jardiance (empagliflozin) Receive the US FDA’s Breakthrough Therapy Designation for the Treatment of Heart Failure with Preserved Ejection Fraction
Shots:
- The designation is based on the P-III EMPEROR-Preserved trial evaluates the safety and efficacy of empagliflozin (10mg, qd) vs PBO in 5,988 patients with chronic HFpEF with/out diabetes
- The results demonstrated a 21% reduction in risk for the composite 1EPs of CV death or hospitalization for adults with HF. The results were presented at ESC 2021 & published in NEJM
- Empagliflozin has previously received FTD from FDA to reduce the risk of CV death and hospitalization for HF & is approved for HFrEF with/out diabetes in the EU & US. Additionally, the companies plan for global regulatory submissions for HFpEF in 2021
Click here to read full press release/ article | Ref: Lilly | Image: Reuters