SI
Schrodinger, Inc. (SDGR)·Q2 2025 Earnings Summary
Executive Summary
- Q2 2025 delivered a revenue and EPS beat vs consensus: total revenue of $54.8M vs ~$52.0M consensus and non-GAAP EPS of -$0.65 vs -$0.77 consensus; GAAP EPS was -$0.59. Management reaffirmed FY25 revenue guidance and lowered full-year OpEx outlook, citing May cost actions and disciplined spend . Values retrieved from S&P Global.*
- Software revenue grew 15% YoY to $40.5M; drug discovery revenue grew 19% YoY to $14.2M. Software gross margin fell to 68% (from 80% YoY) due to predictive toxicology initiative costs and revenue mix .
- Q3 2025 software revenue guidance was set at $36–$40M; FY25 guidance maintained: software growth +10–15%, drug discovery $45–$50M, software gross margin 74–75%, and 2025 OpEx now expected to be lower than 2024 (previously <5% growth) .
- Liquidity strong at ~$462M cash, restricted cash, and marketable securities as of June 30, 2025, supporting runway through pipeline and platform investments; other income swung to +$10.0M on equity marks and interest .
- Post-quarter development risk emerged: SDGR discontinued SGR-2921 (CDC7) after two treatment-related deaths in Phase 1 AML, despite early activity—an overhang for therapeutics narrative near term .
What Went Well and What Went Wrong
What Went Well
- Strong top-line and segment growth: total revenue +16% YoY to $54.8M; software +15% to $40.5M; drug discovery +19% to $14.2M, driven by hosted contracts and contribution revenue, plus collaboration execution (including Novartis amortization) .
- Management reiterated confidence in 2025 outlook and customer demand for validated computational approaches: “our ability to deliver solid second quarter results and maintain our 2025 revenue growth guidance is a testament to our strong customer relationships and the demand for proven computational technologies” — CEO Ramy Farid .
- Pipeline momentum: encouraging initial Phase 1 data for MALT1 inhibitor SGR-1505 with Fast Track for Waldenström macroglobulinemia; plans to complete Phase 1 package and meet FDA for Phase 2 dose; initial data for SGR-3515 and SGR-2921 was expected in Q4 (timing clarity) .
What Went Wrong
- Margin compression: software gross margin fell to 68% (vs 80% YoY, 72% in Q1) due to predictive toxicology costs and revenue mix; margin headwind expected to persist through the grant schedule (roughly two-year cadence starting Q3’24) .
- Continued GAAP losses albeit improved YoY: net loss -$43.2M (vs -$54.0M YoY); operating expenses still high at $79.1M despite sequential reduction from Q1, indicating ongoing investment intensity .
- Macro and cohort headwinds: biotech demand remains challenging; on-prem revenue down YoY due to timing/size of renewals; growth driven by expansions in large pharma while SMID-biotech churn and industry restructuring temper broader uptake .
Financial Results
Headline P&L Comparison (oldest → newest)
Segment Revenue Breakdown
EPS (GAAP and Non-GAAP)
Selected KPIs and Balance Items
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- CEO: “our ability to deliver solid second quarter results and maintain our 2025 revenue growth guidance is a testament to our strong customer relationships and the demand for proven computational technologies to accelerate molecular discovery” .
- CFO: “Broadly, the industry is navigating a complex macroeconomic landscape… Notwithstanding this backdrop, we are very pleased to deliver strong results… We remain well capitalized with $462,000,000 in cash and equivalents as of June 30” .
- Therapeutics lead: “We are very pleased with the initial Phase 1 SGR-1505 data… we plan to complete the Phase 1 package and meet with the FDA later this year to discuss the recommended Phase 2 dose” . “We expect to report initial Phase I data from our other two clinical programs, SGR2921 and SGR3515 in the fourth quarter” .
Q&A Highlights
- Demand and renewals: Large pharma conversations constructive; Q4 is key renewal/scale-up season; biotech cohort remains challenged by macro/regulatory backdrop .
- Predictive tox beta: High interest; collaborators using it; separately priced add-on; feedback cycle ongoing; margin impact tied to grant timing (~2 years from Q3’24) .
- Cost discipline and OpEx: May RIF and expense initiatives driving lower 2025 OpEx vs 2024; sequential OpEx reductions visible in Q2 .
- Pipeline timing: Initial data for SGR-2921 and SGR-3515 clarified as Q4; exploration of strategic opportunities likely for mid/late-stage development across programs .
- Retention: “100% retention rate with customers greater than half a million dollars” reinforcing stickiness at scaled accounts .
Estimates Context
- Beat/miss assessment: Bold revenue and EPS beats vs consensus. The beat was driven by hosted/software contribution revenues and collaboration execution; EPS benefited from reduced R&D OpEx and a swing to other income (equity marks, interest) . Values retrieved from S&P Global.*
- Q3 2025: Consensus total revenue ~$49.62M*; company guided software revenue $36–$40M and expects remaining drug discovery to be roughly evenly split between Q3 and Q4 (definitions differ; total revenue consensus is not directly comparable to software-only guidance) . Values retrieved from S&P Global.*
Guidance Changes
(see table above)
Key Takeaways for Investors
- SDGR delivered a clean beat on revenue and non-GAAP EPS; reaffirmed FY software/drug discovery guidance and lowered OpEx outlook, a positive setup into Q4 renewal season where scale-up discussions are ongoing .
- Expect continued near-term software margin pressure (68% in Q2) as predictive tox contribution revenue carries higher COGS; margin drag should persist through the grant period (~two years from Q3’24) .
- Liquidity (~$462M) provides ample runway for platform and pipeline; other income turned positive on equity marks/interest, partially offsetting operating losses .
- Pipeline narrative bifurcated: SGR-1505 looks promising with Fast Track and initial efficacy signals; however, post-quarter discontinuation of SGR-2921 introduces therapeutics risk and may weigh on sentiment until clarity on 3515 and broader pipeline emerges .
- Trading implications: Near-term, stock likely reacts to the beat and improved OpEx outlook; watch for any pressure from SGR-2921 discontinuation headlines. Q3 software guide ($36–$40M) aligns with seasonal cadence; the stock could hinge on Q4 renewal scale-ups and 3515 data timing .
- Medium-term thesis: Hosted adoption and enterprise-scale deployments at large pharma should structurally reduce Q4 concentration over time; predictive tox monetization and biologics/formulation enhancements broaden TAM despite SMID-biotech headwinds .
- Monitor catalysts: Strategic transaction(s) around SGR-1505, Q4 initial data for SGR-3515, progress in predictive tox commercialization, and late-year renewal outcomes at top accounts .
Disclaimer: Consensus estimates marked with an asterisk (*) are Values retrieved from S&P Global.