Skip to content
ESPR

Esperion Therapeutics, Inc.

Esperion Therapeutics, Inc. Q1 FY2025 earnings call

May 6, 2025 · fiscal period ended 2025-03

EPS · actual vs est

/

Revenue · actual vs est

/
Ask about this call

Summary

Generated 2025-05-06

Management highlights

  • Sales and marketing: US net product revenue up 41% y/y, script growth 2% sequentially. Expanded field reimbursement support team threefold, achieved payer access victories. Bempedoic acid added to 2025 ACC-AHA guidelines. Introduced payer/provider tactics highlighting statin intolerance.
  • International markets: Royalty revenue from Daiichi Sankyo Europe up 8% QoQ. Progress in Europe and Japan, tech transfer for NILEMDO and NUSTENDI progressing. Entered commercial partnerships in Australia/New Zealand, Neopharm Israel filed for approval, Canada submission for NEXLETOL/NEXLIZET.
  • Pipeline: Introduced pipeline targeting primary sclerosing cholangitis (PSC), R&D Day event held, goal to commercialize triple combination in 2027.
View in transcript ↓

Segment performance

Total revenue for the first quarter 2025 grew 63% year-over-year to $65 million after adjusting for a one-time milestone received in Q1 2024. US net product revenue grew 41% year-over-year to $34.9 million. Collaboration revenue was $30.1 million, a decrease of approximately 73% driven by the settlement agreement milestone with DSE, but up 97% excluding the milestone. Royalty revenue from Daiichi Sankyo Europe increased 8% from Q4 2024 to $10.5 million in Q1 2025. As of March 31, 2025, cash and cash equivalents were $114.6 million.

View in transcript ↓

Guidance

  • Full year 2025 operating expense guidance: $215 million to $235 million, including $15 million non-cash stock compensation. Reiterated previous operating expense guidance.
View in transcript ↓

Risks

  • Risks associated with forward-looking statements; actual results may differ due to business risks and uncertainties. Market dynamics, including flat lipid market and seasonal headwinds, pose risks. Regulatory uncertainties in international approvals and pipeline advancement.
View in transcript ↓

Q&A highlights

Q: On BD, when to expect new deal and cash outlook.

A: Not setting timeline for BD, not predicated on Otsuka milestones.

Q: On triple combination vs obicetrapib.

A: Triple combo offers one-pill LDL lowering >60%, focuses on convenience.

Q: Sales force size and education on statin intolerance.

A: 155 sales reps right size, 15 field reimbursement managers added. Education on statin intolerance gaining traction with NLA definition.

Q: Triple combination's place in landscape.

A: Focus on LDL efficacy, lowers hsCRP, right play for market.

Q: ACC-AHA guidelines adoption.

A: Early feedback positive, impacts physician uptake.

Q: Seasonal market dynamics for NEXLETOL/NEXLIZET.

A: Worse than prior years due to IRA and confusion, but improving trends from March.

Q: Gross margin trajectory.

A: Influenced by US vs partner sales, tech transfer to improve margins, cost adjustments in Q1 not recurring in Q2.

View in transcript ↓

Key numbers

Reported versus consensus

Earnings calendar feed

MetricReportedConsensusDeltaPrior year
EPS
Revenue

Transcript

May 6, 2025

Full transcript unavailable for redistribution

The structured summary above covers the available call sections. Full transcript text is not included on this page.

Continue exploring

Prior quarters

This page presents the stored structured earnings-call summary and deterministic earnings calendar values. How this is generated. For informational purposes only; not investment advice.