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Natera, Inc. (NTRA)·Q2 2025 Earnings Summary
Executive Summary
- Strong top-line outperformance and guide raise: Q2 revenue $546.6M (+32.2% y/y) materially beat S&P Global consensus $476.8M; gross margin expanded to 63.4% (+460 bps y/y). FY25 revenue guide raised by $80M at midpoint to $2.02–$2.10B; gross margin guide to 61–64%, OpEx guides held flat . Revenue consensus from S&P Global: $476.8M*.
- Mixed bottom line vs Street: GAAP EPS was ($0.74) vs S&P Global consensus ($0.607), with ~$19.8M legal accruals and
$9.2M SBC estimate change ($0.21/share headwind). CFO noted ~$30M non-cash SBC/legal accruals; ex these, loss/share ~($0.53) . - Operating momentum: Record Signatera growth (+~20k sequential clinical units) and strong ASPs; DSOs improved to a record ~57 days; positive quarterly cash flow ~$24.3M .
- Catalysts: Positive topline from IMvigor011 Phase 3 in bladder cancer (Signatera-guided) announced Aug 18; late-fall ECD PROCEED readout; launch of proprietary AI foundation models to drive diagnostics and pharma partnerships .
What Went Well and What Went Wrong
What Went Well
- Record oncology momentum: “We had a phenomenal quarter… record Signatera growth,” with ~189k oncology tests (+50.6% y/y) and ~+20k sequential growth units; strong new patient starts and broader tumor-type adoption .
- Margin and cash conversion: Gross margin up to 63.4% (vs ~59% LY); DSOs fell to ~57 days with continued revenue “true-ups,” enabling cash generation while investing for growth .
- Product innovation and clinical data: Launched Fetal Focus NIPT for inherited conditions (EXPAND trial showed ~91% sensitivity in early readout), Prospera’s PEDAL study demonstrated monitoring predicts outcomes, and broad Signatera datasets across breast and GI; management highlighted multiple upcoming randomized and guideline-influencing trials .
What Went Wrong
- EPS/EBITDA below Street: GAAP EPS ($0.74) missed S&P Global consensus ($0.607); EBITDA ($100.5M) below consensus ($79.1M). Management cited ~$30M non-cash SBC/legal accruals; ex these, loss/share ~($0.53) .
- Higher OpEx and operating loss: Operating expenses rose 59.2% y/y to $457.0M, with loss from operations widening to $110.4M (vs $43.9M LY), driven by growth investments and legal accruals .
- COGS headwind from first-time patients; sustainability caution: Ex “true-ups,” gross margin was flat q/q given significantly higher exome runs for new Signatera patients; management cautioned +20k quarterly growth units is not a “new normal” .
Financial Results
Headline P&L vs Prior Periods
Revenue and EPS vs S&P Global Consensus
EBITDA vs S&P Global Consensus
Segment/Revenue Mix (where disclosed)
KPIs
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “We had a phenomenal quarter… record Signatera growth… Gross margin ticked up again in Q2 at 63.4%… Raising the revenue guidance by $80,000,000 at the midpoint… We are not increasing our operating expenses” .
- Margin playbook: “We think about margin expansion… revenue cycle operations, expanded coverage… further COGS reductions and AI-driven efficiencies… DSOs are now down to fifty seven days, which is a record” .
- Investment versus returns: New oncology reps added in Q2; 6–12 month “slingshot effect” to productivity; OpEx held steady despite guide raise .
- Pipeline: Prospera PEDAL outcomes monitoring, DARE TOMER strategy in breast, GI publications (GEJ lead-time ~6 months; HCC outperformed AFP with up to 16.5 months lead time) .
Q&A Highlights
- Signatera growth drivers and sustainability: Growth from colorectal, breast, IO monitoring, and expanding to additional histologies; record new patient starts; management cautions 20k quarterly growth units is not the “new normal” .
- Coverage expansion: Non-covered tumor types submissions over next 12–18 months could add ~$250–$300M revenue once covered; multiple submissions planned, data-first approach .
- Early cancer detection timeline: PROCEED advanced adenoma readout late fall; FIND enrollment underway, FDA submission targeted 2027; design aligns screening protocol with FDA trial to mitigate performance degradation risk .
- Sales force expansion: Oncology reps stepped up to ~150–175+ with adds in Q2; productivity expected 6–9 months post-onboarding .
- Policy/regulatory: Proposed MolDx transplant LCD seen as neutral/positive for Prospera; capitation-like dynamics already exist in MRD; cadence largely aligns with clinical practice .
Estimates Context
- Q2 beats/misses vs S&P Global: Revenue $546.6M vs $476.8M* (beat), GAAP EPS ($0.74) vs ($0.607)* (miss), EBITDA ($100.5M) vs ($79.1M)* (miss). Management cited ~$30M non-cash SBC/legal accruals; ex these, loss/share ~($0.53) . Values from S&P Global.*
- Prior quarters: Q1 revenue $501.8M vs $446.7M* (beat); EPS ($0.50) vs ($0.618)* (better than expected). Q4’24 revenue $476.1M vs $447.9M* (beat); EPS ($0.41) vs ($0.385)* (slight miss). Values from S&P Global.* .
- Implications: Raised FY25 revenue/margin guide suggests upward estimate revisions to revenue and modest GM; however, higher first-time patient mix can dampen near-term GM progression, and legal/SBC items introduced EPS variability. Street models likely lift FY25 revenue while reassessing Opex phasing and EBITDA trajectory.*
Key Takeaways for Investors
- The growth engine is intact and broadening: record Signatera sequential units, strong women’s and organ health, and ASP support indicate durable demand drivers .
- Estimate momentum: FY25 revenue guide up to $2.02–$2.10B, with GM 61–64% and positive cash flow maintained—consensus should move higher on revenue and potentially gross margin .
- Watch the mix: First-time patient exome runs are great for future recurring volume but can pressure COGS; management’s four-vector margin plan (RCO, coverage, COGS, AI) is the offset to monitor .
- Coverage catalysts: Submissions for non-covered indications and biomarker-state payers could unlock $250–$300M revenue over time; payor wins and LCD updates are key near-term stock drivers .
- Clinical inflections: Positive IMvigor011 topline (Signatera-guided) and PROCEED advanced adenoma readout in late fall could be material sentiment catalysts for MRD and ECD narratives .
- Operating leverage building: DSOs at a record ~57 days and continued “true-ups” support cash generation while the expanded sales force ramps; OpEx guide held steady despite top-line raise .
- AI optionality: Newly launched AI foundation models could open pharma monetization and drive operational leverage; early pilots outperformed benchmarks .
Additional data and citations:
- Q2 revenue $546.6M; GM 63.4%; tests processed 853.1k; oncology tests 188.8k; cash/cash equivalents/short-term investments/restricted cash ~$1,016.0M; total debt $80.3M .
- Q1 revenue $501.8M; GM 63.1%; tests processed 855.1k; oncology tests 167.7k .
- Q4’24 revenue $476.1M; GM 62.9%; oncology tests 150.8k .
- CFO on non-recurring accruals and EPS ex items .
Values retrieved from S&P Global where marked with an asterisk (*).