| Metric | Value ($ M) | Q2 FY25 | Q3 FY24 |
|---|---|---|---|
| Revenue | 87.31 | 6.0% | 69.1% |
| Total Income | 87.31 | 6.0% | 69.1% |
| Expenditure | 97.27 | 29.2% | 43.8% |
| PBT | — | ||
| Net Profit | -31.33 | 146.1% | 6.1% |
| OPM | -11.41% | 20.02pp | 19.63pp |
| NPM | -35.89% | 20.44pp | 21.30pp |
| EPS | -0.16 | 166.7% | 6.7% |
Esperion Reports Q3 2025 Revenue Up 69% Y/Y to $87.3 Million
04 May 2026 · 4 May, 7:48 am
Summary
Esperion reported a strong Q3 2025 with total revenue increasing by 69% year-over-year to $87.3 million. The growth was driven by increased U.S. prescription volume and expanded payer coverage. The company reached a settlement agreement with Dr. Reddy’s Laboratories, ensuring market exclusivity for NEXLETOL and NEXLIZET until 2040. Bempedoic acid also received a Class I, Level A recommendation in the 2025 ESC/EAS guidelines. Esperion expects to achieve sustainable profitability beginning in the first quarter of 2026.
Key Highlights
- 1
Esperion's total revenue for Q3 2025 grew by 69% year-over-year to $87.3 million.
- 2
U.S. net product revenue for Q3 2025 increased by 31% year-over-year to $40.7 million.
- 3
Collaboration revenue for Q3 2025 increased by approximately 128% year-over-year to $46.7 million.
- 4
A settlement agreement was reached with Dr. Reddy’s Laboratories, preventing generic versions of NEXLETOL and NEXLIZET until April 2040.
- 5
Bempedoic acid received a Level 1a recommendation in the updated ESC/EAS Guidelines for Management of Dyslipidemias.
- 6
Partner Otsuka received regulatory approval and favorable preliminary pricing to market NEXLETOL in Japan, triggering significant milestone payments upon final pricing approval.
Management Comments
Sheldon Koenig
"Our third quarter performance reflects consistently strong execution across our commercial, clinical, and global expansion strategies. We delivered robust year-over-year revenue growth, driven by increased U.S. prescription volume and expanded payer coverage, now reaching over 90% of commercial lives and more than 80% of Medicare lives. The recent settlement agreement with Dr. Reddy’s, along with earlier settlements with three other ANDA filers, supports our ability to build and maintain our market leadership for many years to come. We’re seeing strong momentum in healthcare practitioner engagement and patient access, driven by innovative consumer campaigns and a strategic focus on statin intolerance. We’re building on this success through targeted investments that expand our commercial momentum." “The inclusion of bempedoic acid as a Class I, Level A recommendation in the 2025 ESC/EAS guidelines marks a pivotal moment in cardiovascular risk management. We believe this recognition will be reflected similarly in the upcoming U.S. guidelines expected in the first quarter of 2026. In anticipation of this and our extended patent runway, throughout the third quarter we invested in enhanced payer access, expanded sales and marketing initiatives, and patient access programs to ensure that we are leveraging these advantages to drive revenue growth and build a blockbuster franchise.”
Informational and educational content only. Not investment advice.