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GLAUKOS Corp (GKOS)·Q1 2025 Earnings Summary
Executive Summary
- Record Q1 2025 net sales of $106.7M (+25% YoY; +26% constant currency) with U.S. Glaucoma $59.1M (+41% YoY) and International Glaucoma $29.0M (+15% YoY; +19% cc); non-GAAP gross margin ~82% .
- Results beat Wall Street consensus: Revenue $106.7M vs $102.8M*, and non-GAAP EPS ($0.22) vs ($0.35); EBITDA also better than consensus, driving guidance reaffirmation of FY25 net sales $475–$485M . Values retrieved from S&P Global.*
- Management highlighted strong early adoption of iDose TR, broadening MAC reimbursement, and methodical rollout to commercial/Medicare Advantage; reiterated iDose ramp as a key 2025 growth driver .
- Headwinds: MIGS LCDs continue to pressure U.S. stents (non‑iDose revenues guide to down mid‑single digits), FX and emerging competition internationally, and MDRP impact in corneal health .
- Stock reaction catalysts: iDose TR reimbursement milestones (additional MACs adding professional fees), Epioxa NDA acceptance with Oct 20, 2025 PDUFA, and PRESERFLO 510(k) pivotal study initiation .
What Went Well and What Went Wrong
What Went Well
- Strong top-line beat and broad-based growth: Q1 net sales $106.7M (+25% YoY), record U.S. Glaucoma $59.1M (+41% YoY), International Glaucoma $29.0M (+15% YoY) .
- iDose TR momentum: “We are pioneering a brand-new therapeutic category that has the potential to reshape glaucoma management” — Tom Burns; iDose J-code payment streamlining in multiple MACs and professional fee schedules expanding .
- Non-GAAP profitability trajectory improved: operating loss ($15.2M) vs ($32.8M) prior year; non-GAAP EPS ($0.22) vs ($0.70) prior year; benefited from lower amortization and absence of prior IPR&D charge .
What Went Wrong
- U.S. stent franchise impacted by LCDs: “modestly more pronounced than expected... we saw a mid-single-digit decline year-over-year” in Q1; full-year non-iDose revenues expected down mid-single digits .
- International FX and competitive trialing headwinds expected to increase through 2025, moderating growth vs 2024’s strong performance .
- Corneal Health pressured by MDRP: Q1 corneal health $18.5M (+1% YoY) but ongoing realized revenue impact; management guides to flat–low single-digit growth in 2025 .
Financial Results
Segment breakdown
KPIs
Estimates comparison (S&P Global)
Narrative: Revenue beat driven by iDose TR adoption and broader glaucoma execution; EPS beat reflects revenue leverage and lower amortization (no IPR&D charge vs prior year) while opex growth remained controlled .
Guidance Changes
Underlying assumptions include MIGS LCD headwinds, Hydrus royalty expiration on Apr 26, 2025, continued MDRP impact, and FX headwinds; iDose TR ramp and broader IG initiatives expected to offset .
Earnings Call Themes & Trends
Management Commentary
- “We are reaffirming our full year 2025 net sales guidance range of $475 million to $485 million…with strong performance driven by iDose TR adoption” — Tom Burns .
- “Professional fee schedules…Noridian first, and now Novitas and First Coast…we are seeing continued solid and expanding growth” — Joe Gilliam .
- “We successfully advanced execution of our detailed launch plans for iDose TR…growing number of trained surgeons and accounts…market access among MACs, commercial, and Medicare Advantage payors” — Prepared remarks .
- “We manufacture and source primarily within the U.S., and as such, expect minimal direct exposure to the most recently implemented tariff-related policies” — Quarterly Summary .
Q&A Highlights
- U.S. stent headwinds: mid‑single‑digit YoY decline in Q1; guide to non‑iDose down mid‑single digits for 2025 as LCD restrictions persist, offset by stand‑alone iStent infinite .
- iDose pacing: Q1 implied ~$21M run-rate; momentum supported by MACs turning on pro fees (Noridian, Novitas, First Coast), broadening J-code payment consistency; methodical rollout to commercial/Medicare Advantage .
- Guidance components: International glaucoma HSD–LDD; corneal health flat–LSD; modestly higher iDose expectations embedded; seasonality skewed to H2 .
- Readministration & next-gen: iDose PAS filed with 6‑month FDA timeline; TREX advancing as de facto reimplantation path if needed .
- OpEx: ~15% YoY growth in 2025 off 2024 base; path to margin accretion from iDose volumes by late 2025 .
Estimates Context
- Q1 2025: Revenue beat ($106.7M vs $102.8M*), non-GAAP EPS beat (($0.22) vs ($0.35)), EBITDA ahead of consensus; strength from iDose ramp and glaucoma execution. Values retrieved from S&P Global.*
- Near-term expectations: Management indicated Q2 quarter weighting ~23–24% with continued iDose progress and expanding MAC reimbursement .
Where estimates may need to adjust:
- Raise iDose trajectories modestly given expanding MAC pro fees and consistent J-code payment in more regions .
- Temper U.S. stent (non‑iDose) revenues to down mid‑single digits for 2025 given LCDs and Hydrus royalty expiration .
- Moderate international growth for FX and competitive trialing; maintain HSD–LDD .
Key Takeaways for Investors
- Q1 print demonstrated durable revenue momentum and a clear beat; reaffirmed FY25 guide anchors the iDose-led growth narrative .
- The iDose reimbursement cadence is improving across MACs; watch for additional professional fee schedules and J-code consistency—key near-term stock catalysts .
- Expect non‑iDose U.S. stent pressure through 2025 (LCDs, Hydrus royalty expiry), but stand‑alone iStent infinite utilization and combo cataract iDose use should partially offset .
- International growth normalizing from 2024 highs; FX and competitive trialing warrant conservative models (HSD–LDD) .
- Corneal health is stabilizing (flat–LSD) ahead of potential Epioxa approval; PDUFA Oct 20, 2025 provides optionality for 2026 growth and portfolio balance .
- Margin trajectory improving; management targets ~15% OpEx growth and sees iDose manufacturing scaling as the path to margin accretion late 2025 .
- Tactical: Near term, the stock is likely to trade on iDose reimbursement milestones and monthly utilization trends; medium term, pipeline events (Epioxa, PRESERFLO, TREX) expand optionality and support multiple .
Additional Relevant Press Releases (Q1 2025)
- FDA acceptance of Epioxa NDA; PDUFA Oct 20, 2025 .
- Collaboration with RadiusXR and Topcon to expand patient access to vision diagnostics (Inspire platform) .