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Recursion Pharmaceuticals, Inc.
NASDAQ: RXRX Healthcare Pharma 🔎 Screen
$1.6B
Market Cap
P/E
PEG
-127.8%
ROCE
-59.5%
ROE
0.06
D/E
-867.9%
OPM
-48.6%
% from 52W High
21
α RS
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🌏 Global Investor Returns
Currency-adjusted total returns for RXRX including FX impact
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About

Recursion Pharmaceuticals, Inc., a clinical-stage biotechnology company, engages in the decoding biology and chemistry by integrating technological innovations across biology, chemistry, automation, data science, and engineering to industrialize drug discovery in the United States and the United Kingdom.

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📈 Growth Pattern
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⭐ Superinvestors Holding RXRX
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Manager Shares Value % of Fund Period
Cathie Wood ARK Investment Management 40.21M $123.5M 0.96% Mar 2026
Jim Simons Renaissance Technologies LLC 2.40M $7.4M 0.01% Mar 2026

SEC Form 13F data. 45-day lag from quarter end.

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🎙 Management Tone Confident Specific → Stable 4 quarters Full tone analysis in Intelligence →
📊 MIXED Recursion advances AI-driven drug pipeline with $665M cash runway through early 2028.
Revenue & Profitability
Recursion reported a 30% year-over-year reduction in cash operating expenses and ended Q1 2026 with $665 million in cash equivalents. Cash OpEx guidance for 2026 remains less than $390 million. The company expects operating runway through early 2028 without additional financing. No revenue, net income, or operating income figures were disclosed in the transcript.
Outlook
Management focused on translating AI platform advantages into clinical proof points, emphasizing that only about 10% of biology is understood by the industry. They view the potential to unlock intractable diseases through foundation models and large-scale multimodal maps. No explicit macroeconomic tailwinds or headwinds were discussed; the call centered on internal milestones and platform progress.
Growth Drivers
Key growth drivers include the wholly owned pipeline with five programs (REC-4881 for FAP, REC-1245 for solid tumors/lymphoma, REC-4539 for small-cell lung cancer/AML) each having clear catalysts over the next 12-18 months. Partner programs with Sanofi (chemistry AI for difficult targets) and Roche (biology maps for novel targets) are advancing toward opt-in decisions and development candidate milestones. Clinical development AI tools are shown to accelerate trial enrollment by 30-60% and expand eligible patient populations by up to 40%.
Balance Sheet & CapEx
Not discussed in detail. The call noted continued investment in the platform (compute, data generation, models) but without specific CapEx figures. Management stated they invest 'surgically' in areas that differentiate the platform, such as clinical AI, chemistry design models, and biology foundation models (TxPert, TxFM).
Margins
Not discussed explicitly. The company highlighted a 30% year-over-year reduction in cash operating expenses achieved through operational discipline and infrastructure simplification. No gross margin or operating margin figures were provided, but the focus on capital allocation and efficiency suggests a trajectory toward improved operating leverage as programs advance.
Key Risks
Key risks flagged include regulatory uncertainty for first-in-disease programs (e.g., REC-4881 in FAP) where no clear precedent exists, requiring close FDA alignment on endpoints. For REC-1245, potential hematotoxicity is a concern, though no Grade 3 heme tox has been seen to date. The company's ability to achieve opt-ins from partners remains an execution risk, though progress is being made.
Generated by AI · Q1 2026 results · Not investment advice
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✓ 📞 Earnings Call Transcripts (5 quarters) submit a missing quarter
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📞 Earnings Call Transcripts (5)
Q2 2026 Q2 2026 2026-08-05
Reached a pivotal stage with five clinical programs and over $500M in partnership inflows. Lowered 2026 OpEx guidance by 40% and maintained a $557M cash runway. Advanced key assets in FAP and oncology, while partnerships validated the AI-native engine's ability to discover novel targets.
Q1 2026 Q1 2026 2026-05-06
AI-driven platform advances have led to clinical proof in multiple programs, strong partner inflows, and a 30% reduction in operating expenses. Cash runway extends into early 2028, with multiple clinical milestones and regulatory engagements expected in the next 12-18 months.
Q4 2025 Q4 2025 2026-02-25
First AI-enabled clinical proof of concept achieved in FAP, with strong progress across a diversified pipeline and $500M+ in partnership inflows. Operating expenses reduced 35% year-over-year, extending cash runway to early 2028.
Q3 2025 Q3 2025 2025-11-05
Leadership transition and strong financial discipline position the company for sustained growth, with $785M in cash and a runway through 2027. Key milestones include a $30M Roche/Genentech payment, robust pipeline progress, and continued AI-driven innovation.
Q2 2025 Q2 2025 2025-08-05
Integrated Exscientia and Recursion platforms have accelerated drug discovery, with strong cash reserves and multiple clinical and partnership milestones achieved. Guidance remains unchanged, with a cash runway through Q4 2027 and several key readouts expected in the next 18 months.
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Financial Model
Projections are built from each company's audited annual financials (Income Statement, Balance Sheet, Cash Flow) over the last 5 fiscal years. Forward assumptions — revenue growth %, EBITDA margin, D&A (USD millions), interest expense, tax rate, and capex — are AI-generated using historical context and refreshed twice a year: after the December results season and after the September/Q4 results season.

DCF Valuation
Fair Value = Σ(FCFt / (1+WACC)t) + Terminal Value. Terminal Value uses the Gordon Growth Model: FCF5 × (1+g) / (WACC−g). Default WACC: 10% (US risk-free ~4.5%, equity risk premium ~5.5%). Default terminal growth: 3% (long-run US nominal GDP proxy).

CAGR Tracker
Expected 5-year CAGR = (DCF Fair Value / Current Price)1/5 − 1. Assumes fair value is reached in exactly 5 years — a mechanical estimate only.

Data Sources & Limitations
Financial statements sourced from public filings. Prices updated daily. Forward assumptions are AI-generated. All monetary values in USD millions. Non-US ADR companies may have currency conversion inaccuracies. Models are point-in-time and do not update intra-quarter or account for M&A, macro shocks, or extraordinary items.

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Investment Risk:
Investing in securities, including US equities and ETFs, involves inherent risks including the potential loss of principal. All investments are subject to market fluctuations, economic conditions, regulatory changes, and other factors that may affect their value. Past performance is not indicative of future results. This analysis is provided for informational and educational purposes only and should not be construed as investment advice under any circumstances.

No Investment Recommendation:
This analysis does not constitute, nor should it be interpreted as, an offer, solicitation, or recommendation to buy, sell, or hold any securities or financial products. Investors are strongly advised to conduct their own independent research and due diligence and to consult with a licensed financial advisor or an SEC-registered investment adviser before making any investment decisions, taking into account their individual financial situation, risk tolerance, and investment objectives.

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Conflict of Interest Disclosure:
The author and/or analyst may currently hold or have previously held positions in the securities discussed. Any such positions are not intended to influence the objectivity or independence of the analysis. This research is produced independently and is not sponsored, endorsed, or commissioned by any company or institution.

Information Sources:
The analysis is based on publicly available information including SEC filings (10-K, 10-Q), annual reports, management commentary, and publicly available financial data. Information is believed to be accurate as of the date of publication but may be subject to change without notice. Readers are encouraged to independently verify all information before acting upon it.

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