$RXRX earnings report

Sanofi optioned the first development candidate from its collaboration with Recursion, triggering a $10 million milestone payment to be recognized as revenue in the third quarter of 2026. AlphAI read Recursion Pharmaceuticals's third quarter of 2026 filing as solid. 2 quarters are on record below.

third quarter of 2026

AlphAI · Earnings readRXRX · third quarter of 2026

Sanofi optioned the first development candidate from its collaboration with Recursion, triggering a $10 million milestone payment to be recognized as revenue in the third quarter of 2026.

✓Solid quarter

The filing reports a meaningful collaboration milestone, revenue recognition of a $10 million payment in the third quarter of 2026, and transfer of further development and commercialization responsibility to Sanofi. It does not provide a complete quarterly financial-results release.

Revenue
$10M

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
Sanofi option milestone paymentother$10M––
Milestone payment to be recognized as revenue in the third quarter of 2026other$10M––
Total upfront and milestone payments received from Sanofi under the collaborationother$144M––
Additional potential milestones for the optioned programothermore than $300 million––
Progress-based milestones achieved across the Recursion-Sanofi collaborationothersix progress-based milestones across five programs––

2027 and over the next 12 months outlook

  • NoteThe candidate is expected to enter phase 1 clinical trials in 2027.
  • NoteOver the next 12 months, other programs in the joint portfolio have the potential to reach development candidate and other progress-based milestones.

What drove it

  • Sanofi optioned the first development candidate from the companies’ multi-program research collaboration.
  • The potential first-in-class oral small molecule was designed against a challenging dual target implicated in inflammatory disease.
  • The candidate was delivered through Recursion’s integrated AI-enabled drug design platform and small-molecule chemistry capabilities combined with Sanofi’s drug-discovery and immunology expertise.
  • Sanofi will fund and lead further development and commercialization of the optioned candidate.
  • The option ends Recursion’s operational requirements related to this candidate, with all future payments resulting in profit to Recursion.

Concerns

  • The candidate is expected to enter phase 1 clinical trials in 2027 and remains subject to clinical-development, safety, efficacy, regulatory, and commercialization risks.
  • Sanofi retains discretion over option exercises, program advancement, and funding and may delay, deprioritize, or discontinue development of the optioned candidate.
  • More than $300 million in additional milestones and royalties are contingent on future program progress and successful commercialization.
  • The filing contains no complete income statement, cash flow statement, balance sheet, or quarterly operating-expense disclosure.

What to watch

  • Recognition of the $10 million milestone payment as revenue in the third quarter of 2026.
  • Initiation of the optioned candidate’s planned phase 1 clinical study in 2027.
  • Potential development-candidate and other progress-based milestones from additional programs in the joint portfolio over the next 12 months.
  • Sanofi’s continued funding and advancement of the optioned program.

Balance sheet and cash flow

  • The $10 million milestone payment will be recognized as revenue in the third quarter of 2026.
  • Sanofi’s selection of the development candidate triggered a $10 million milestone payment to Recursion.

Analysis

This Item 2.02 filing is a collaboration-development update rather than a complete quarterly earnings release. Sanofi optioned the first development candidate from the companies’ multi-program research collaboration, triggering a $10 million milestone payment. Recursion states that this payment will be recognized as revenue in the third quarter of 2026, but the filing does not report total third-quarter revenue or any other complete quarterly financial results.

The option raises total upfront and milestone payments received from Sanofi under the collaboration to $144 million. The companies have achieved six progress-based milestones across five programs. Recursion remains eligible for more than $300 million in additional milestones for the optioned program, along with an average of low double-digit royalties on net product sales if it is successfully commercialized.

The operational structure changes favorably for Recursion on the optioned program: Sanofi will fund and lead further development and commercialization, while the option ends Recursion’s operational requirements related to this candidate. Recursion states that all future payments related to the candidate will result in profit to Recursion. The candidate has been added to Sanofi’s development pipeline and is expected to enter phase 1 clinical trials in 2027.

The milestone supports the stated utility of Recursion’s platform in progressing a complex dual-target small-molecule design program. The company attributes delivery of the candidate to iterative computational prediction, chemical design, synthesis, and experimental validation, combined with Sanofi’s drug-discovery and immunology expertise. The filing also identifies further potential milestone activity, stating that other joint-portfolio programs could reach development-candidate and other progress-based milestones over the next 12 months.

The principal limitation is that the filing provides no total revenue, expenses, profitability, cash balance, cash flow, or balance-sheet data for the third quarter of 2026. The future economic value remains contingent on development progress, clinical outcomes, regulatory approval, commercialization, and Sanofi’s decisions on funding and program prioritization.

Management, verbatim

The most important test of any technology platform in drug discovery is whether it can translate into differentiated medicines. Together with Sanofi, we tackled a difficult design problem against a dual target product profile with high potential and delivered a molecule that Sanofi has now selected for its development pipeline. With additional programs advancing across our collaboration, this milestone is another important demonstration of how our platform can translate computational capabilities into differentiated medicines — and do so repeatedly.

Najat Khan, Ph.D., President and Chief Executive Officer of Recursion

By combining Sanofi's drug discovery and clinical and translational knowledge in Immunology with Recursion's AI-driven platform, we were able to move with speed and precision in a space where that balance is notoriously hard to achieve. This new development candidate has potential to deliver a differentiated oral medicine with highly selective dual targeting that could be a meaningful advance for people living with inflammatory diseases who still lack adequate treatment options.

Alyssa Johnsen, Therapeutic Area Head, Development, Immunology & Inflammation, Sanofi

Not in the filing

stated, not guessed
  • Period-end date for the third quarter of 2026
  • Total revenue for the third quarter of 2026
  • Revenue comparison with the prior-year period
  • Revenue comparison with the prior quarter
  • Gross profit and gross margin
  • Operating expenses
  • Operating income or loss
  • Net income or loss
  • GAAP earnings or loss per share
  • Non-GAAP earnings or loss per share
  • Operating cash flow
  • Free cash flow
  • Cash and cash equivalents
  • Debt
  • Share repurchases
  • Dividends
  • Revenue, margin, operating-expense, or tax-rate financial guidance
  • Prior guidance for comparison

AlphAI analysis generated from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure was cross-checked against the filing text; consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

Second Quarter 2026

AlphAI · Earnings readRXRX · Second Quarter 2026 · ended June 30, 2026

Recursion Reports Second Quarter Financial Results; Genentech Options First Neuroscience Target into Early Discovery Program

→Mixed quarter

Revenue was $7.7 million versus $19.2 million in the prior-year quarter, while research and development expenses decreased to $89.6 million from $128.6 million and 2026 cash operating expense guidance was reduced to <$375 million.

Revenue
$7.7M

Key metrics

shortened, hover for the filing’s print
MetricValueq/qy/y
Total revenueGAAP$7.7M––
Research and development expensesGAAP$89.6M––
Cash, cash equivalents and restricted cashother$556.8M––
Roche and Genentech collaboration upfront and milestone payments to dateother$216M––
Sanofi collaboration upfront and milestone payments to dateother$134M––

2026 outlook

  • Operating expenses<$375 million
  • NoteBased on current operating plans with no additional financing, the Company continues to expect its cash runway to extend into early 2028.

What drove it

  • Roche and Genentech revenue recognized was less in the current period due to the successful completion of certain project phases in the prior period.
  • Research and development expenses decreased primarily due to lower platform costs resulting from the timing of Tempus record purchases.
  • Genentech exercised the first Validated Target Option under the companies' neuroscience collaboration, advancing a previously unexplored neuroscience target into a small molecule early discovery program.
  • REC-7735 was precision designed to show >100-fold selectivity for the H1047R mutant over wild type.
  • The REC-7735 development candidate was delivered in 10 months and 242 compounds from first novel hit through Recursion's AI-native design platform.
  • Agent-supported enrollment strategies contributed to a 1.3 to 1.6x increase in enrollment rates versus historical benchmarks.

Concerns

  • Total revenue was $7.7 million for the second quarter of 2026, compared to $19.2 million for the second quarter of 2025.
  • Cash, cash equivalents and restricted cash were $556.8 million as of June 30, 2026 compared to $753.9 million as of December 31, 2025.
  • The supplied filing text ends during the explanation of research and development expenses, before the complete financial-results disclosure and financial statements.

What to watch

  • An update to define the registrational path for REC-4881 is expected in 2H26.
  • Additional Phase 2 safety and efficacy data from the TUPELO clinical trial will be presented in November 2026.
  • The Phase 1/2 ZINNIA clinical study for REC-7735 is expected to be initiated in the second half of 2026.
  • Additional Phase 1 dose escalation data for REC-1245 are expected in 2H26.
  • Potential differentiated AI-enabled oral molecules could reach development candidate and late-stage discovery milestones with Sanofi over the next 6-12 months.

Balance sheet and cash flow

  • Cash, cash equivalents and restricted cash were $556.8 million as of June 30, 2026 compared to $753.9 million as of December 31, 2025.
  • Based on current operating plans with no additional financing, the Company continues to expect its cash runway to extend into early 2028.

Analysis

Second-quarter revenue was $7.7 million, compared to $19.2 million in the second quarter of 2025. The company attributed lower Roche and Genentech revenue recognition to successful completion of certain project phases in the prior period. The result underscores that reported collaboration revenue can vary with the timing of project milestones and completion phases.

Research and development expenses decreased to $89.6 million from $128.6 million. Recursion cited lower platform costs resulting from the timing of Tempus record purchases as a primary driver. The company also reduced 2026 cash operating expense guidance to <$375 million from <$390 million, placing expense control alongside continued pipeline development.

Cash, cash equivalents and restricted cash were $556.8 million as of June 30, 2026, compared with $753.9 million as of December 31, 2025. Management stated that, based on current operating plans with no additional financing, its cash runway is expected to extend into early 2028. No operating cash flow, free cash flow, debt, repurchase, or dividend data were included in the supplied text.

Operationally, Genentech exercised the first Validated Target Option in the neuroscience collaboration and advanced a previously unexplored target into a small molecule early discovery program. Recursion also reported an IND clearance for REC-7735 and expects to initiate its Phase 1/2 ZINNIA study in the second half of 2026. Near-term execution points include the expected REC-4881 registrational-path update in 2H26, additional REC-4881 Phase 2 data in November 2026, REC-7735 trial initiation, and additional REC-1245 Phase 1 data in 2H26.

Management, verbatim

Recursion has reached a pivotal point where our AI-native platform is translating unique data into potential first-in-class therapeutic opportunities.

Najat Khan, Ph.D., Chief Executive Officer of Recursion

Not in the filing

stated, not guessed
  • Gross profit and gross margin
  • Selling, general and administrative expenses
  • Total operating expenses
  • GAAP operating income or loss
  • Non-GAAP operating income or loss
  • GAAP net income or loss
  • Non-GAAP net income or loss
  • GAAP earnings or loss per share
  • Non-GAAP earnings or loss per share
  • Weighted-average shares outstanding
  • Operating cash flow
  • Free cash flow
  • Debt balances
  • Share repurchases
  • Dividends
  • Revenue, gross margin, tax rate, and other financial guidance beyond 2026 cash operating expense guidance
  • Prior outlook document for guidance comparison
  • Complete remaining financial-results disclosure, as the supplied filing text ends mid-sentence

AlphAI analysis generated from the company’s SEC earnings filing (Form 8-K Item 2.02, or Form 6-K for a foreign private issuer). Every figure was cross-checked against the filing text; consensus estimates, price targets and share-price reactions are not shown because they are not in the filing. AI-generated research, not investment advice.

Questions about RXRX earnings dates

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