Recursion Pharmaceuticals, Inc. (RXRX) SEC Filings & Earnings Calls
EquiReason read 18 Recursion Pharmaceuticals, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-15 — Recursion entered an underwriting agreement to sell 61.54M shares at $3.25/share, raising ~$200M gross. Dilution of ~20% based on prior shares outstanding. Cash balance ~$561M post.
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
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- Next earnings
- 11 Nov, in 18 days
Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
15 Oct 20268-K · 1.01, 2.02, 7.01, 8.01Recursion entered an underwriting agreement to sell 61.54M shares at $3.25/share, raising ~$200M gross. Dilution of ~20% based on prior shares outstanding. Cash balance ~$561M post-ATM sales. Sanofi optioned a development candidate.open
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and restricted cash · Q3-2026 | $561M |
Risks flagged
Dilution from equity offering
“61.54M shares at $3.25/share; ~20% dilution”
21 Sep 20268-K · 1.01Recursion amended its Master Agreement with Tempus AI, extending term to 6 years, revising annual fees to $14M, and entered a TxFM License Agreement granting Tempus a non-exclusive license for $12M.open
Figures in the filing · each found in the filing text
| Annual License Fee · FY2026 | $14M | |
| License Fee · FY2026 | $12M |
Risks flagged
Elimination of termination for convenience reduces flexibility.
“eliminate the Company’s right to terminate the Agreement for convenience” · word for word
5 Aug 20268-K · 2.02, 7.01Q2 2026 revenue $7.67M vs $19.22M prior year; net loss $131M; Genentech advanced first neuroscience target; reduced 2026 cash operating expense guidance to <$375M from <$390M.earningsopen
Figures in the filing · each found in the filing text
| Total revenue · Q2-2026 | $8M | -60% y/y |
| Net loss · Q2-2026 | $-131M | -24% y/y |
| Cash and cash equivalents · Q2-2026 | $546M | |
| Research and development expense · Q2-2026 | $90M | -30% y/y |
| General and administrative expense · Q2-2026 | $42M | -11% y/y |
Guidance
FY26 cash operating expense guidance reduced to <$375M from <$390M
Reduced 2026 cash operating expense guidance by $15 million to <$375 million based on identified operating efficiencies.
Risks flagged
Revenue decline and continued operating losses raise cash burn concerns.
“Total revenue decreased from $19.2M to $7.7M year-over-year; net loss of $131M in Q2 2026.”
Dependence on partnership milestones for non-dilutive funding; any delay could pressure cash runway.
“Partnership milestones from Roche/Genentech and Sanofi are key revenue sources; guidance cut suggests cost control.”
5 Aug 202610-QRecursion reported Q2 2026 results with net loss improving 24% YoY to $131M, driven by significant cost reductions across R&D and G&A.earningsopen
Figures in the filing · each found in the filing text
| Total revenue · Q2-2026 | $8M | -60% y/y |
| Net loss · Q2-2026 | $-131M | +24% y/y |
| Net loss per share · Q2-2026 | $-0.25 | +39% y/y |
| Cash and cash equivalents · 2026-06-30 | $546M | |
| Research and development expense · Q2-2026 | $90M | -30% y/y |
| General and administrative expense · Q2-2026 | $42M | -11% y/y |
| Operating cash flow · H1-2026 | $-187M | +10% y/y |
| Free cash flow · H1-2026 | $-187M |
Risks flagged
Cash runway uncertainty
“The Company expects to incur substantial operating losses in future periods and will require additional capital to advance its drug candidates.” · word for word
Revenue concentration on partnerships
“Operating revenue is generated through research and development agreements derived from strategic alliances.” · word for word
Material weakness in internal controls
“Our disclosure controls and procedures were ineffective due to the material weaknesses in internal control over financial reporting disclosed in Part II, Item 9A of our Annual Report on Form 10-K for the year ended December 31, 2025.” · word for word
6 May 202610-QQ1 2026 results: revenue down 56% YoY, net loss improved 42% YoY, cash burn reduced; pipeline progress with positive data for REC-4881 and REC-1245.earningsopen
Figures in the filing · each found in the filing text
| Total revenue · Q1-2026 | $6M | -56% y/y |
| Net loss · Q1-2026 | $-118M | +42% y/y |
| Cash used in operating activities · Q1-2026 | $-81M | -39% y/y |
| Cash, cash equivalents and restricted cash · 2026-03-31 | $665M | |
| Research and development expense · Q1-2026 | $88M | -32% y/y |
| General and administrative expense · Q1-2026 | $35M | -37% y/y |
Risks flagged
No approved products; reliance on partnerships and equity financing
“We do not have any products approved for commercial sale and have not generated any revenues from product sales.” · word for word
Accumulated deficit of $2.2 billion
“As of March 31, 2026, our accumulated deficit was $2.2 billion.” · word for word
Need for additional financing
“We anticipate that we will need to raise additional financing in the future to fund our operations, including the potential commercialization of any approved product candidates.” · word for word
30 Apr 20268-K · 5.02, 7.01Reported the departure of a director or principal officer (CEO/CFO change); issued a Regulation FD disclosure (forward guidance or material update)open
Risks flagged
Founder departure from Board could signal strategic shift, but remains as advisor
“Chris Gibson will not stand for re-election to the Board”
30 Apr 2026DEF 14AProxy statement filed for 2026 annual meeting; includes CEO transition, compensation details, and director compensation policy updates.open
Figures in the filing · each found in the filing text
| Total Shareholder Return (Cumulative, $100 invested at IPO) · FY2025 | $13.07 | |
| Net Income (Loss) · FY2025 | $-645M | |
| Compensation Actually Paid to PEO · FY2025 | $3M | |
| Average Compensation Actually Paid to Non-PEO NEOs · FY2025 | $-518662.00 |
25 Feb 202610-KRisks named: Supply Chain Disruption, Regulatory Compliance Costopen
Risks flagged
Supply Chain Disruption
“certain of our specialized equipment, as well as the API used in our drug candidates, are obtained from single-source suppliers” · word for word
Regulatory Compliance Cost
“We are subject to numerous environmental, health and safety, and other laws and regulations” · word for word
Clinical Development Failure
“Our business is dependent on the successful development of our current and future product candidates”
25 Feb 20268-K · 2.02, 7.01Cash, cash equivalents and restricted cash $754Mearningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and restricted cash · FY2025 | $754M |
Risks flagged
No revenue, net loss, cash burn typical for clinical-stage biotech
“No revenue or net income figures provided; company is pre-revenue”
Clinical trial risk: pipeline failure could impair value
“Dependence on clinical trial outcomes; no approved products”
12 Jan 20268-K · 7.01Issued a Regulation FD disclosure (forward guidance or material update); filed financial statements and exhibits with this reportopen
Risks flagged
Forward-looking statements; no specific risk signals in excerpt
“Boilerplate safe harbor language.”
8 Dec 20258-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Clinical trial risk; early-stage data may not support regulatory approval or commercial success.
“Phase 1b/2 trial; no specific results disclosed in filing; typical biotech development risk.”
26 Nov 20258-K · 8.01Shares registered for resale 7,088,742open
Figures in the filing · each found in the filing text
| shares registered for resale · Q4-2025 | 7,088,742 |
Risks flagged
Potential dilution from share issuance for license fees; no cash raised
“7,088,742 shares...issued to Tempus AI, Inc. in payment for annual license fees”
5 Nov 202510-QRecursion reported Q3 2025 revenue of $5.2M (down 80% YoY) and net loss of $162.3M (widened 69% YoY), reflecting milestone timing and higher costs from Exscientia acquisition.earningsopen
Figures in the filing · each found in the filing text
| Total Revenue · Q3-2025 | $5M | -80% y/y |
| Net Loss · Q3-2025 | $-162M | +69% y/y |
| Cash and Cash Equivalents · 2025-09-30 | $660M | |
| Operating Cash Flow · 9M-2025 | $-326M | +34% y/y |
Risks flagged
No approved products; ongoing losses
“We do not have any products approved for commercial sale and have not generated any revenues from product sales.” · word for word
Dependence on future financing
“We anticipate that we will need to raise additional financing in the future to fund our operations.” · word for word
Revenue volatility from milestone timing
“The timing of revenue recognition is not directly correlated to the timing of cash receipts.” · word for word
5 Nov 20258-K · 2.02, 5.02, 7.01Released earnings results and quarterly financials; reported the departure of a director or principal officer (CEO/CFO change)earningsopen
Risks flagged
Leadership transition risk; new CEO may shift strategy.
“CEO change announced; no financial impact quantified.”
29 Oct 20258-K · 8.01Acceptance Fee $30Mopen
Figures in the filing · each found in the filing text
| Acceptance Fee | $30M |
Recursion Pharmaceuticals, Inc. — questions
- What did Recursion Pharmaceuticals, Inc. file recently?
- 18 SEC filings in the last 12 months. Latest: 8-K on 2026-10-15 — Recursion entered an underwriting agreement to sell 61.54M shares at $3.25/share, raising ~$200M gross. Dilution of ~20% based on prior shares outstanding. Cash balance ~$561M post-ATM sales. Sanofi optioned a development candidate.
Every figure on this page comes from Recursion Pharmaceuticals, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.