IT
iRhythm Technologies, Inc. (IRTC)·Q1 2025 Earnings Summary
Executive Summary
- Q1 2025 revenue was $158.7M, up 20.3% YoY, with gross margin of 68.8% (+250 bps YoY). GAAP EPS was $(0.97) vs $(1.47) a year ago; adjusted EBITDA was $(2.6)M, an improvement from $(12.1)M in Q1 2024 .
- Versus S&P Global consensus, revenue beat ($158.7M vs $153.4M*), while EPS was roughly in line/slightly below (($(0.95) vs $(0.94)* on an adjusted/consensus basis) .
- FY25 guidance raised: revenue to $690–$700M (from $675–$685M) and adjusted EBITDA margin to 7.5%–8.5% (from 7.0%–8.0%). Q2 EBITDA margin guided to 6%–7%; full-year gross margin expected flat due to tariff headwinds of ~50–75 bps .
- Key drivers: sustained Zio AT momentum (now ~14% of revenue) and upstream primary care adoption (>1/3 of LTCM volumes); catalysts include Zio MCT FDA submission targeted for Q3 2025 and Epic Aura rollouts showing early 20–40% prescribing uplift at integrated accounts .
What Went Well and What Went Wrong
What Went Well
- Strong top-line and margin expansion: Revenue +20.3% YoY to $158.7M; gross margin 68.8% (+250 bps YoY). CEO: “revenue growth exceeding 20% year-over-year” driven by demand for Zio monitor and Zio AT, with record demand in the UK .
- Product/Channel momentum: Zio AT delivered the strongest quarter ever; management tied Q1 outperformance primarily to Zio AT growth. Primary care channels now account for over one-third of LTCM volumes, expanding the total addressable pool .
- International and clinical evidence catalysts: Commercial launch in Japan (PMDA-cleared AI) and AVALON real-world evidence in >428k commercially insured patients reaffirming diagnostic yield and reduced retesting/CV events for Zio LTCM vs other modalities/providers .
What Went Wrong
- Profitability still negative: GAAP net loss $(30.7)M and adjusted EBITDA $(2.6)M; incremental costs include FDA remediation/DOJ-related expenses (~$15M expected for FY25) and IP litigation costs (excluded from non-GAAP beginning Q1) .
- Tariff headwinds and FCF: Tariffs expected to be a ~50–75 bps annual GM headwind; inventory builds to mitigate supply risk create slight FY25 FCF headwind; FCF positive targeted for FY26 .
- Japan reimbursement: Initial rate aligned to Holter (not differentiated), reducing FY25 contribution below the prior ~$2M plan; company will generate local evidence to pursue improved reimbursement .
Financial Results
Quarterly trend (last three quarters)
Year-over-year comparison (Q1 2024 vs Q1 2025)
Estimates vs Actuals (Q1 2025)
*Values retrieved from S&P Global.
KPIs and Mix (selected)
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “The first quarter of 2025 demonstrated continued commercial momentum, with revenue growth exceeding 20% year-over-year, driven by… our Zio AT business” — Quentin Blackford, CEO .
- “Adjusted EBITDA… negative 1.7% of revenue… 750 basis-point improvement… result of… sustainable efficiency at scale” — Dan Wilson, CFO .
- “Our commercial launch in Japan… first ambulatory cardiac monitoring solution to utilize a 14-day PMDA-cleared artificial intelligence in arrhythmia detection… initial reimbursement… Holter monitoring rate… we intend to generate additional clinical evidence… to support future reimbursement applications” — CEO .
- “In a handful of [Epic-integrated] accounts… high 20% increase… some… almost 40%… our guide does not anticipate any incremental benefit” — CEO .
Q&A Highlights
- Guidance raise above the beat reflects durable Zio AT momentum; upside from innovative channels remains less predictable and mostly not embedded yet .
- Japan FY25 contribution now below prior ~$2M expectation given Holter-level reimbursement; local head-to-head evidence planned to pursue higher rates .
- Zio AT share gains appear driven by product advantages and ease of trial in existing monitor accounts, not only competitor disruptions; 14-day continuous wear differentiates vs competitors .
- Epic Aura: Early evidence of prescribing uplift (high 20% avg, up to ~40%); not included in guidance until more data accumulated .
- Regulatory: MCT submission still targeted for Q3; FDA leadership consistent at senior levels; remediation on track .
- Tariffs: 50–75 bps GM headwind contemplated; supply-chain strategies prioritized over price increases; inventory build to ensure continuity .
Estimates Context
- Q1 2025 revenue beat consensus ($158.7M vs $153.4M*) while EPS was in line/slightly below (($(0.95) vs $(0.94)*). Management raised FY25 revenue guidance to $690–$700M from $675–$685M and lifted EBITDA margin range to 7.5%–8.5% from 7.0%–8.0%, implying upward bias to revenue and margin models from here .
- Q2 color: ~25% of full-year revenue expected in Q2 and adjusted EBITDA margin of 6%–7%; full-year GM flat due to tariffs suggests consensus gross margin should remain near current levels despite mix improvements .
- FY25 FCF slightly negative (inventory builds and platform investments); FY26 FCF positive target noted for long-term models .
*Values retrieved from S&P Global.
Key Takeaways for Investors
- Zio AT is the incremental growth engine now; management attributes Q1 outperformance primarily to AT, with share gains likely continuing into 2H if momentum persists .
- Upstream primary care penetration (>1/3 of LTCM volumes) and innovative risk-bearing channels (early stage) expand the TAM and support durable double-digit growth beyond cardiology/EP .
- Epic Aura integration is a potential 2H tailwind; early 20–40% prescribing uplift in integrated accounts is not in guidance, setting up optionality for upside if rollout scales .
- Guidance upgrade and Q2 phasing (25% of FY) improve near-term visibility; full-year GM flat outlook and tariffs (50–75 bps) temper margin expansion near term .
- Japan launch is strategically important; near-term revenue tempered by Holter-rate reimbursement, but evidence-building plan targets future pricing improvement .
- Regulatory de-risking continues: remediation on track; senior FDA continuity; MCT filing remains a 2H catalyst .
- Liquidity remains strong ($520.6M cash/securities); FCF slightly negative in FY25 on inventory build and platform investments, turning positive in FY26, supporting continued execution .
Appendix: Additional Press Releases (Q1 2025 window)
- Japan commercial launch of Zio LTCM (PMDA-cleared AI, 14-day monitoring); nationwide availability targeted by July 2025 via Senko .
- AVALON real-world analysis (>428k patients) showed higher diagnostic yield, fewer retests, and fewer CV events for Zio LTCM vs other modalities/providers in a commercially insured population .