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Vicarious Surgical Inc. (RBOT)·Q1 2025 Earnings Summary
Executive Summary
- Q1 2025 was execution-heavy: first patient cart and surgeon console built, instrument sets produced and moving into biocompatibility/sterility testing; dossier filing targeted for mid-2025; first human cases still expected later in 2025 .
- Cash and investments ended at $37.4M; cash burn was $11.7M; full-year 2025 cash burn guidance reiterated at approximately $50M .
- GAAP EPS of -$2.60 missed Wall Street consensus of -$2.48; adjusted EPS was -$2.58; company remains pre-revenue (no revenue reported) .
- Catalysts: mid-year technical dossier submission, first-in-human cases later in 2025, plus incremental hospital partnerships (UMass Memorial); NYSE “below criteria” notice adds listing overhang until compliance plan progresses .
What Went Well and What Went Wrong
What Went Well
- Built first patient cart and surgeon console; second set underway for first human case; instrument sets produced and entering biocompatibility/sterility testing, indicating tangible progress toward clinical readiness .
- Maintained timeline confidence: technical dossier filing targeted mid-2025; initial human cases later in 2025; endpoint aligned with pivotal trial (ventral hernia repair completion) .
- New hospital partnership with UMass Memorial to optimize perioperative workflows, education, and adoption—expands ecosystem beyond prior partners (HCA, University Hospitals, Intermountain Health, LSU Health) .
Management quote: “We are increasingly optimistic that the progress made in the first quarter will enable us to showcase the groundbreaking value of our V1.0 system in a clinical setting later this year.”
What Went Wrong
- EPS missed consensus; pre-revenue status continues with operating loss driven by R&D and G&A investments .
- NYSE continued listing standard notice (average market cap < $50M and stockholders’ equity < $50M) adds a listing risk overhang pending submission and acceptance of a compliance plan .
- Financing remains a focus: CFO acknowledged active evaluation of financing options and intent to align a raise around upcoming milestones—supportive insider base noted but still a capital-raising need .
Analyst concern: timeline queries on dossier review assumptions and supply chain stability; management indicated dossier mid-year with baked-in review cycles and supply chain challenges from last quarter have been managed without schedule changes .
Financial Results
KPIs
Versus Estimates (S&P Global)
Values retrieved from S&P Global.*
YoY and Sequential context:
- YoY: Adjusted EPS flat at -$2.58; GAAP EPS improved versus -$2.90 (Q1’24) on lower warrant liability impact and opex moderation .
- Sequential: GAAP EPS deteriorated to -$2.60 from -$2.36 (Q4’24) as operating expenses ticked up sequentially from $15.0MM to $15.7MM .
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- Strategic focus: “We anticipate 2025 will be the year Vicarious Surgical evolves into a clinical stage company... Our efforts are directed toward the precise and timely execution of all critical intermediate steps essential for our success in the clinic.”
- Clinical plan: “We expect to treat a handful of patients at a few sites... The endpoint... will align with that of our pivotal trial, focusing on the surgeon's ability to successfully complete the intended ventral hernia repair.”
- Regulatory timing: “We’re looking around mid this year at filing our technical dossier... We feel fairly confident... that does bake in some time to go back and forth.”
- Financing posture: “We’re currently evaluating all options... very supportive insider base... hoping to structure a financing around [upcoming milestones].”
- Supply chain tone: “We have not seen any further changes or adjustments in our schedule as a result of supply... we are feeling quite good about our supply chain.”
Q&A Highlights
- Financing runway and approach: CFO emphasized disciplined spend, supportive insiders, and pursuit of financing aligned to milestones—signals likely capital raise around dossier/first-patient catalysts .
- Supply chain execution: Prior quarter’s gating issues resolved; no schedule adjustments from supply; team managing complex supply chain effectively .
- Dossier review timing: Filing mid-year with baked-in Q&A cycles based on precedents; confidence in assumptions and timeline .
- Hospital partners’ role: Partnerships primarily enhance perioperative workflow design, education, and future commercial adoption; clinical value to be demonstrated later this year .
Estimates Context
- Q1 2025 EPS: Consensus -$2.48* vs GAAP actual -$2.60 (miss). Adjusted EPS -$2.58 matched adjusted actual. Revenue consensus $0.0*; company remains pre-revenue .
- Prior quarter Q4 2024 EPS: Consensus -$2.69* vs GAAP actual -$2.36 (beat) .
- With dossier mid-year and first patients later this year, near-term estimate revisions likely hinge on opex cadence and any incremental financing costs; revenue remains $0 until clinical/commercial milestones are achieved .
Values retrieved from S&P Global.*
Key Takeaways for Investors
- Near-term catalysts: mid-2025 dossier submission and first-in-human cases later in 2025—execution on these should drive stock reaction; watch for pre- and post-event financing .
- Pre-revenue profile persists; EPS volatility tied to opex and non-operating items (e.g., warrant liability fair value); adjusted metrics track core spending .
- Operational momentum: consoles built; instruments produced and entering testing; supply chain stabilized—improves confidence in clinical readiness .
- Partnership flywheel: UMass Memorial adds to ecosystem, focusing workflow and education—supports future adoption narrative once commercial .
- Listing overhang: NYSE continued listing notice introduces headline risk during cure period; compliance plan submission due within 45 days; 18-month window .
- Guidance steady: FY25 cash burn ~$50M maintained; watch quarterly burn pacing and capital planning against milestones .
- Trading setup: Shares likely sensitive to regulatory timeline confirmations, any financing announcement terms, and progress updates on initial patient cases; downside risk from slippage of dossier/clinical timing or unfavorable listing developments .