RECURSION PHARMACEUTICALS, INC. (RXRX): what the price assumes
In the published model solve dated 2026-Q2, anchored at $3.18, RECURSION PHARMACEUTICALS, INC. (RXRX) is priced for today's economics sustained for ~40.0 years+. boothcheck publishes no house fair value, target price, or buy/sell rating; individual model outputs and user-controlled scenarios are analytical inputs, not Boothcheck targets. Narrative composed 2026-06-28.
Generated: 2026-08-10 · Exported: 2026-08-12 · Source: https://boothcheck.com/report/RXRX
Headline
| Field | Value |
|---|---|
| Ticker | RXRX |
| Company | RECURSION PHARMACEUTICALS, INC. |
| Current price | $3.18/sh |
| Composition | United States 53% / United Kingdom 47% / Other 0% |
What The Price Assumes (Inversion)
The assumption today's price embeds, recovered by inverting the valuation.
| Field | Value |
|---|---|
| Inversion basis | revenue-multiple |
| EV / sales paid | 16.7x |
| Steady-state operating margin assumed | 9.2% |
Beyond 25%/yr sustained for 40 years; not resolvable as a revenue bet. The inversion reports a bound, not a solved point.
The company earns no operating profit yet; the inversion runs on the revenue multiple and an assumed steady-state margin.
Solve inputs: computed at a 15.6% cost of capital; growth searched up to the 25% self-funding ceiling.
Reconcile: at the x-ray's 9.3% required return this reads ~19.4 years; the models below use their own rates.
How unusual the bet is: n/a
| Reference | Value |
|---|---|
| vs own history | -0.83σ |
| sustained it ~5 years at this level | 35% |
| implied end-window share | 0% |
Valuation X-Ray
Every valuation family lands below the price. The price therefore sits beyond what those standard frames encode.
How the valuation models price the stock relative to the market price. Price/FV above 1.0 means the market pays more than that lens defends (expensive); at or below 1.0 the lens can defend the price.
| Family | Median price/FV | Models | Reads |
|---|---|---|---|
| Asset | 1.73x | 2 | expensive |
| Earnings | — | 0 | — |
| Relative | 6.36x | 2 | expensive |
| Growth | 5.26x | 2 | expensive |
Families that call it expensive: Asset, Relative, Growth
The models below discount at their own flat-beta convention rates (cost of equity 9.3%, WACC 8.9%); the inversion above states its own rate.
Per-Model Detail (n=6)
| Model | Family | FV | Price/FV | Applicable | Methodology |
|---|---|---|---|---|---|
| DCF Perpetual Growth | Growth | $0.00 | — | no | Negative/zero FCF — equity value floored at $0 |
| DCF Exit Multiple | Growth | $0.00 | — | no | Negative/zero FCF or EBITDA — equity value floored at $0 |
| Relative Valuation | Relative | $0.50 | 6.36x | yes | P/S fallback (negative EPS): Sector P/S 4.0x × TTM revenue — excluded from consensus |
| Simple DDM | Growth | — | — | no | — |
| Two-Stage DDM | Growth | — | — | no | — |
| Simple Excess Return | Asset | $1.94 | 1.64x | yes | Book value floor: BV/sh $1.94, ROE negative |
| Two-Stage Excess Return | Asset | $1.74 | 1.83x | yes | Book value with convergence: BV/sh $1.94, ROE converges to ke |
| Discounted Future Market Cap | Growth | $2.73 | 1.16x | yes | Rev $0.1B, growth 30% (input: historical growth; tapered), Terminal P/S: 10.5x / 15.0x / 19.5x (bear / base = today's held flat / bull, cap 15x) |
| Peter Lynch Fair Value | Relative | $0.00 | — | no | Negative/zero EPS — earnings-based value floored at $0 |
| Margin Trajectory | Growth | $0.34 | 9.35x | yes | Margin ramp: -50% → 12% over 7yr, rev growth 30% (input: historical growth; tapered) |
| Earnings Power Value | Earnings | — | — | no | — |
| Residual Income | Asset | — | — | no | — |
| Graham Number | Asset | — | — | no | — |
| EV/EBITDA Relative | Relative | — | — | no | — |
| FCF Yield | Earnings | — | — | no | — |
| SBC-Adj FCF Yield | Earnings | — | — | no | — |
| Ben Graham Formula | Earnings | — | — | no | — |
| ROIC-Justified P/B | Asset | — | — | no | — |
| P/Sales Sector | Relative | $0.50 | 6.36x | yes | Revenue $0.07B × sector P/S 4.0x |
| PEG Fair Value | Relative | — | — | no | — |
| Earnings Yield | Earnings | — | — | no | — |
| Funds From Operations Multiple | Relative | — | — | no | — |
| Clinical Phase NPV | Growth | — | — | no | — |
| Merton | Asset | — | — | no | — |
| V5 Mechanical | — | — | — | no | — |
Economic-Unit Decomposition (Sum Of The Parts)
Only one reportable economic unit is present in the current topology source. Consolidated operating lenses remain available, but there is no multi-unit decomposition.
| Unit | Role | Valuation basis | Revenue | Reported profit | Value evidence | Status |
|---|---|---|---|---|---|---|
| Recursion Pharmaceuticals (consolidated) | operating | enterprise | 0.1B reported-currency | — | withheld | unresolved no unit value |
No total common-equity value is stated. One or more material units lack a supported unit value. The displayed values are an indicative subtotal; consolidated debt and cash cannot be applied to a fraction of the company.
Solvency
| Field | Value |
|---|---|
| Net cash | $636.1m |
| Interest coverage | -354.3x |
| Share count CAGR (dilution) | 32.7% |
| Burning cash | yes |
Operating profit is negative or near zero and the company has no demonstrated through-cycle (mid-cycle) operating margin to normalize against, so years-to-repay cannot be computed honestly.
Bullet Takeaways
- Recursion is a clinical-stage company trying to industrialize drug discovery with AI and automated biology; it has no approved product, generates only partnership revenue, and runs deep operating losses.
- The merger with Exscientia extended the cash runway into early 2028 and targets about $100 million in annual synergies, which is what funds the next wave of trials.
- The watch list is clinical: roughly seven readouts over 18 months across oncology and rare diseases, with the REC-4881 TUPELO data and an FDA registration-pathway discussion in the first half of 2026 the most important.
Bull Case
No standard valuation method reaches Recursion's price, and that is the correct starting point, because this is not a company to value on trailing financials. It is a bet on a platform. Recursion is trying to do something the pharmaceutical industry has wanted for decades: turn drug discovery from artisanal trial-and-error into an engineered, repeatable process, using automated biology experiments at scale and machine learning to find drug candidates faster and cheaper. If that works even partially, the value is not in today's $70 million of partnership revenue; it is in a discovery engine that can generate candidate after candidate at lower cost than the traditional model.
The combination with Exscientia is what gives the bet more shots on goal. The merger extended the cash runway into early 2028 and targets about $100 million in annual synergies, and the company expects roughly seven clinical readouts over the following 18 months across oncology and rare diseases. Seven readouts is a portfolio, not a single binary, which is the point of an industrialized platform: spread the risk across many programs so the failure of any one does not sink the thesis. The TUPELO data for REC-4881 was framed as the first clinical validation of the latest version of the platform, the kind of proof point the bull case needs.
The balance sheet buys the time to find out. Recursion holds about $636 million of cash against almost no debt, and it cut quarterly cash operating expense to $85.1 million in Q1 2026 from $120.2 million a year earlier, extending the runway without new financing into early 2028. Partnerships with large pharmaceutical companies provide non-dilutive milestone income and external validation of the platform. The bull case is simple to state and hard to underwrite: if the AI-discovery engine produces even one or two approvable drugs from this pipeline, the platform is worth a large multiple of today's price, and the company has the cash to reach the readouts that would prove it.
Bear Case
Recursion has no approved drug, no product revenue beyond partnership payments, and it loses hundreds of millions of dollars a year. That is the structural truth, and it has to lead, because every optimistic projection runs through a pipeline of candidates that have not yet proven they work in humans at the scale required for approval. The bear case is not that the platform will fail outright; it is that meaningful commercial success is years away in even a plausible scenario, and the price is being set as if the AI-discovery thesis is closer to proven than it is. The filing is direct that the candidates "may not be successful and may not receive regulatory approval or market acceptance."
The dilution is the second hard fact. The share count has grown about 33% a year, an enormous rate, because a pre-revenue company that burns cash funds itself by issuing stock and by merging with other cash-consuming companies. Even with the runway extended into early 2028, the math of a clinical-stage biotech is that more capital will eventually be needed, and each raise dilutes existing holders further. An investor buying today is buying a slice that the company's own financing needs are likely to keep shrinking. The filing also flags dependence on others for manufacturing and distribution, which can "adversely affect our future profit margins and our ability to commercialize any products that receive marketing approval."
The valuation sits at the most demanding end of the scale. With no operating profit, the price is read against sales at roughly 25 times revenue, a bound so extreme that no standard frame supports it; the methods that anchor on assets, peers, or forward growth all land below the price, and the book-value floor is near $1.94 per share. The asset-value methods are the only ones close, which tells you the cash on the balance sheet is doing much of the work holding the price up. The seven upcoming readouts are genuine catalysts, but they are also seven chances to disappoint, and clinical data in oncology and rare disease fails far more often than it succeeds. The bear does not need to call the platform a fraud; it only needs to note that a cash-burning, heavily diluting, pre-commercial company priced for a 40-year revenue runway has to deliver clinical wins on a schedule that history says is the exception, not the rule.
Valuation
Pinning a value on a pre-commercial company is inherently speculative, and this report does not try. The company is not earning a normal operating profit, so the price is read against sales, and at roughly 25 times revenue the implied path is extreme: it would require revenue growth beyond 25% a year sustained for decades and an eventual operating margin in the high single digits. That is a bound, not a solved number, and the engine flags the read as the most demanding end of the scale. The honest framing is that standard valuation arithmetic against trailing fundamentals is the wrong tool here; the price is an option on a platform, not a multiple of a business.
The methods confirm there is no value-method support near the price. No family reaches it: the relative and growth lenses land well below, and only the asset-value methods come close, anchored on a book value near $1.94 per share that is mostly the cash on the balance sheet. In other words, the part of the price the methods can justify is roughly the cash; the rest is the market paying for the discovery platform and the pipeline, which no standard frame can value because the candidates have not been approved. That is the correct way to read it, not as the model failing, but as the model isolating how much of the price is demonstrated value and how much is the bet.
Solvency here is about runway, not leverage. Recursion holds about $636 million of cash against almost no debt, but it is burning cash, with quarterly cash operating expense of $85.1 million in Q1 2026. On the current plan that funds the company into early 2028, which is the window in which the pipeline has to produce convincing clinical data. The share count growing about 33% a year is the cost of that runway. What a buyer underwrites at this price is not a discounted stream of profits; it is the probability-weighted value of an AI-discovery platform reaching commercial drugs before the cash and the patience run out.
Catalysts
The catalyst calendar is dense and clinical. Recursion expects roughly seven clinical readouts over 18 months following the Exscientia merger, spanning oncology and rare diseases, which turns the next year and a half into a series of binary events. The most advanced is REC-4881: the TUPELO trial data was presented as the first clinical validation of the latest platform version, the company plans to engage the FDA in the first half of 2026 on a registration pathway, and additional data is expected in early 2027. Earlier-stage assets including RBM39, CDK7, ENPP1, MALT1, and LSD1 carry safety, pharmacokinetic, or go/no-go decisions over the next 18 to 24 months.
The corporate catalyst already in hand is the Exscientia integration. The merger extended the cash runway into early 2028 and targets about $100 million in annual synergies, and Recursion cut quarterly cash operating expense to $85.1 million in Q1 2026 from $120.2 million a year earlier. Partnerships with large pharmaceutical companies remain a source of non-dilutive milestone income and validation.
What to watch is each clinical readout and the FDA interaction on REC-4881, because positive data on even one or two programs would reprice the platform thesis, while failures would erode it. Given the cash-burn profile, the runway into early 2028 is itself a clock: the pipeline has to produce convincing results inside that window. The next readout and the FDA pathway discussion are the near-term events that move the story.
Peer Cohorts (Per Segment, With Filing Citations)
Recursion Pharmaceuticals (consolidated) (reported)
- EDIT (Editas Medicine, Inc.)
- FY2025 10-K: …and development services, option payments, milestone payments, and royalty payments to or from the Company. Collaboration Revenue As of December 31, 2025, the Company's contract liabilities were primarily related to the Company's collaboration with BMS. The following table presents changes in the Company's accounts…
- FY2025 10-K: …government regulations, development by competitors of technological innovations and ability to transition from pilot-scale manufacturing to large-scale production of products. Liquidity As of December 31, 2025, the Company has raised an aggregate of $ 1.1 billion in net proceeds through the sale of shares of its…
- BEAM (Beam Therapeutics Inc.)
- FY2025 10-K: $ ( 1,626 ) $ 3,852 Contingent consideration liabilities assumed in acquisition $ 7,715 $ - $ - Fair value of equity instruments issued in connection with acquisition $ 6,715 $ - $ - The accompanying notes are an integral part of these consolidated financial statements F- 8 Beam Therapeutics Inc. Notes to consolidated…
- FY2025 10-K: …business planning, raising capital and providing general and administrative support for these operations. The Company is subject to risks and uncertainties common to early-stage companies in the biotechnology industry including, but not limited to, technical risks associated with the successful research, development…
- VIR (Vir Biotechnology, Inc.)
- FY2025 10-K: …Early adoption permitted. The Company early adopted ASU 2025-07 on a prospective basis in 2025. Reclassification Certain reclassifications have been made to prior period amounts on the Company's consolidated balance sheet to conform to the current period presentation and enhance comparability. As a result, certain…
- FY2025 10-K: …Company and Amunix Pharmaceuticals, Inc., dated July 31, 2024 10-Q 001-39083 10.1 11/04/2024 10.66† F irst Amendment to the License Agreement between the Company and Amunix Phar maceuticals, Inc., date d April 14, 2025 10-Q 001-39083 10.1 11/05/2025 10.67† License Agreement between the Company and Norgine Pharma UK…
- IMCR (Immunocore Holdings plc)
- FY2025 10-K: …net, chargebacks are recorded as a reduction in accounts receivable. Other chargebacks, rebates and deductions are recognized in Accrued expenses and other current liabilities in the Consolidated Balance Sheets. F-10 Table of Contents In certain countries, the Company's customers are hospitals and healthcare…
- FY2025 10-K: …was also required in the assessment of rebates payable. We applied judgement to assess internal targets, pricing information of other therapies approved for sale in France, information obtained from price negotiations of KIMMTRAK in other countries, and information connected with KIMMTRAK's safety profile when…
- NUVB (Nuvation Bio Inc.)
- FY2025 10-K: …broad, we may not be able to compete effectively in our market. • Our reliance on third parties requires us to share our trade secrets, which increases the possibility that a competitor will discover them or that our trade secrets will be misappropriated or disclosed. • We may become involved in lawsuits to protect…
- FY2025 10-K: 741 ( 145 ) Comprehensive loss $ ( 205,387 ) $ ( 567,547 ) The accompanying notes are an integral part of the consolidated financial statements. F- 5 NUVATION BIO INC. and Subsidiaries CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY (In thousands, except share data) Convertible Preferred Stock Common Stock and…
- STOK (Stoke Therapeutics, Inc.)
- FY2025 10-K: (k) of the Internal Revenue Code (the "401(k) Plan"). The 401(k) Plan covers all employees who meet defined minimum age and service requirements 120 and allows participants to defer a portion of their annual compensation on a pretax basis. The Company matches contributions up to 4 % of annual salary for those…
- FY2025 10-K: …and capital expenditure requirements through at least twelve months from the issuance date of these consolidated financial statements. 2. Summary of significant accounting policies and recent accounting pronouncements Basis of presentation and consolidation The accompanying consolidated financial statements have been…
- OCUL (Ocular Therapeutix, Inc.)
- FY2025 10-K: 1,016 851 Payments of debt refinancing costs - - ( 5,184 ) Proceeds from issuance of common stock upon public offering, net of issuance costs 539,585 - 117,261 Repayment of MidCap notes payable - - ( 26,125 ) Repayment from issuance of short-term bridge loan - - …
- FY2025 10-K: …financial statements. F-4 Table of Contents OCULAR THERAPEUTIX, INC. CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (In thousands, except share and per share data) Year Ended December 31, 2025 2024 2023 Revenue: Product revenue, net $…
- RYTM (RHYTHM PHARMACEUTICALS, INC.)
- FY2025 10-K: …from those estimates. Principles of Consolidation The consolidated financial statements include the accounts of Rhythm Pharmaceuticals, Inc. and its wholly-owned subsidiaries. All significant intercompany balances and transactions have been eliminated in consolidation. Segment Information Operating segments are…
- FY2025 10-K: …Drug Rebate Program, the assumptions related to the inputs utilized as well as management's review of the application of the government pricing regulations. Our audit procedures to test the allowances for rebates owed pursuant to the Medicaid Drug Rebate Program included, among others, procedures to assess the…
Methodology Note
- Priced-in inversion: the valuation is inverted on the current price to recover the operating-income growth, duration, and steady-state margin the price embeds (ROE for financials, FFO growth for REITs).
- Valuation x-ray: the valuation models, grouped into four families (asset, earnings, relative, growth). Each model is expressed as a price/FV ratio (distance from price), not a point fair-value estimate. The spread across families is the disagreement.
- Economic-unit decomposition (SOTP): each disclosed business unit is assigned its native valuation basis before any multiple is applied. Operating units are valued on enterprise value; funded financial units are valued on their own common equity, because their borrowings fund earning assets rather than levering the parent. A company total is stated only once every material unit carries a supported value and the parent capital bridge reconciles.
- Solvency: net cash/debt, net-debt-to-NOPAT, interest coverage, and share-count CAGR from EDGAR financials (net debt / FFO and fixed-charge coverage for REITs; regulatory-capital framing for financials).
- Peer cohorts: per-segment comparables with deep-linkable SEC filing citations.
Fundamentals sourced from SEC EDGAR filings. Current price from Databento. The priced-in inversion and valuation x-ray are computed by the boothcheck engine; narrative composed by AI from the structured data.
Sources
Recursion Q1 2026 update, March 2026 · Recursion 2025 results, March 2026