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AVITA Medical, Inc. (RCEL)·Q1 2025 Earnings Summary
Executive Summary
- Q1 2025 commercial revenue was $18.5M, up 67% year over year, with gross margin 84.7%; net loss improved to $13.9M (-$0.53 per share) versus -$18.7M (-$0.73) in Q1 2024 .
- Versus Street, revenue missed consensus by ~$2.17M and EPS missed by ~$0.19; management reaffirmed FY25 revenue guidance of $100–$106M, FCF in H2, and GAAP profitability in Q4 2025. The misses were driven by product mix (Cohealyx/PermeaDerm revenue share), volume discounts, and inventory reserve, partially offset by opex actions (>$2.5M/qtr reduction) . Revenue/EPS consensus values marked with an asterisk and sourced from S&P Global.*
- Strategic catalysts: full commercial launch of Cohealyx (Apr 1), RECELL GO mini rollout (Feb), PermeaDerm manufacturing insourced and revenue-share improved (60% to AVITA), plus proposed CMS NTAP for RECELL (potential Oct 1) .
- Liquidity and covenants: cash and marketable securities declined to $25.8M (from $35.9M at FY-end). AVITA obtained a waiver of the Q1 TTM revenue covenant ($73M) and reset future covenant levels, keeping FY25 guidance unchanged .
What Went Well and What Went Wrong
What Went Well
- Portfolio expansion and adoption: “We are no longer a single product burn-only company… fully integrated multiproduct platform” with RECELL GO mini and Cohealyx launched; addressable market expanded to >$3.5B .
- Opex discipline and path to profitability: management expects opex reductions of ~$2.5M per quarter and reiterated FCF in H2 and GAAP profitability in Q4 2025 .
- Clinical/operational validation: early Cohealyx cases showed 7-day graft readiness and reduced length of stay; PermeaDerm manufacturing moved in-house; distribution terms improved (AVITA now retains 60% of ASP) .
What Went Wrong
- Consensus miss: Q1 revenue (
$18.5M) below consensus ($20.7M*) and EPS (-$0.53) below consensus (-$0.32*), reflecting product mix shifts, volume discounts, and inventory reserves; overall gross margin fell to 84.7% vs 86.4% prior-year . Revenue/EPS consensus values marked with an asterisk and sourced from S&P Global.* - Cash usage was higher than anticipated in Q1 due to bonuses/commissions and payroll resets; cash & marketable securities decreased by ~$10.1M q/q to $25.8M .
- Vitiligo commercialization paused amid reimbursement uncertainty; management guided to no revenue dependence from vitiligo near term .
Financial Results
Quarterly Performance vs Prior Periods and Consensus
Q1 2025 vs Q1 2024 (YoY)
Q1 2025 Actual vs Wall Street Consensus (S&P Global)
Values retrieved from S&P Global.*
Segment/Breakdown
- Reported mix commentary (not numerical): Cohealyx (50% ASP share) and PermeaDerm (60% ASP share) reduce overall gross margin %, while RECELL-only gross margin remained ~86.4% in Q1 2025 .
KPIs and Operating Metrics
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “We are no longer a single product burn-only company… fully integrated multiproduct platform positioned to lead in therapeutic acute wound care… U.S. addressable market… more than $3.5 billion annually.” — CEO Jim Corbett .
- “Overall, we expect to save $2.5 million per quarter in operating expenses and improve operating margin, all while increasing our selling capacity.” — CEO Jim Corbett .
- “Gross margin for RECELL products only was 86.4% for the quarter… overall gross margin percentage will decrease… as the percentage of our revenue derived from new products increases.” — CFO David O’Toole .
- “We reiterate our full year 2025 commercial revenue guidance of $100 million to $106 million… expect to generate free cash flow in the second half… achieve GAAP profitability during Q4.” — CFO David O’Toole .
Q&A Highlights
- Cohealyx rollout: limited Q1 release validated 7-day graft readiness; full SKU set available since Apr 1; post-market Cohealyx I enrolling to provide outcomes and cost-effectiveness data .
- RECELL GO mini adoption: early inventory placement at trauma accounts; sized for <480 cm² wounds (~2.5% TBSA); multi-product portfolio improves trauma surgeon engagement .
- Sales coverage: reconfigured to ~70 selling roles with market development specialists; aim to be present in both stages of the two-stage procedure to sell dermal matrix, RECELL and PermeaDerm .
- Revenue cadence: management models “even sequential growth” with some back-half weighting as VAC approvals for Cohealyx ramp .
- Vitiligo: spending paused; continue discussions with payers but no revenue dependence in forecasts until a reimbursement path is defined .
Estimates Context
- Q1 2025 revenue missed consensus ($20.67M*) by ~$2.15M; EPS missed consensus (-$0.321*) by ~$0.194, driven by lower overall gross margin from mix (Cohealyx/PermeaDerm revenue share), volume discounts, and higher inventory reserve . Values retrieved from S&P Global.*
- With FY25 revenue guidance reaffirmed ($100–$106M) and the opex run-rate reduction (~$2.5M/qtr), Street models may need to rebalance quarterly cadence to reflect sequential growth with greater back-half weighting (VAC-driven Cohealyx contributions) .
Key Takeaways for Investors
- Near-term setup: Despite Q1 misses vs consensus, portfolio breadth (RECELL GO mini, Cohealyx, PermeaDerm) plus opex cuts and proposed NTAP support a back-half inflection; FY25 guidance maintained .
- Margin dynamics: Expect RECELL-only GM to remain mid-80s while overall GM stays lower on mix; operating margin should benefit as distribution revenues scale without proportional opex increases .
- Cash/covenants: Liquidity declined in Q1, but covenant relief secured; monitor cash burn trajectory and execution of opex reductions into H2 .
- Adoption catalysts: Cohealyx consignment/RFID, clinical data read-through (Cohealyx I), and RECELL GO mini address trauma use-cases (<480 cm²), supporting sequential growth .
- Reimbursement optionality: CMS NTAP (if approved) could enhance RECELL economics from Oct 1; EU CE mark for RECELL GO expected mid-2025 .
- Execution watchpoints: Sales model transition and VAC throughput are critical to ramp non-RECELL revenues; management indicated potential breakout of non-RECELL sales by Q3, implying meaningful mix shift .
- Medium-term thesis: Integrated acute wound care platform increases ASP per case and TAM (> $3.5B U.S.); if AVITA delivers on adoption and efficiency plan, pathway to sustained profitability strengthens .
Values retrieved from S&P Global.*