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Recursion Pharmaceuticals (RXRX) Q3 2026 Earnings Report

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MX:RXRX Q3 2026 EPS Results

Actual EPS
-MXN 4.09
Consensus EPS
-MXN 4.07
Beat/Miss
Missed by -MXN 0.02
One Year Ago EPS
-MXN 6.70

MX:RXRX Q3 2026 Revenue Results

Actual Revenue
MXN 345.12M
Expected Revenue
MXN 275.43M
Beat/Miss
Beat by +MXN 69.69M
YoY Revenue Growth
+258.49%

Earnings Announcement Details

Quarter
Q3 2026
Date
11/02/2026
Time
After Close
Conference Call
Monday, November 2, 2026
MX:RXRX Upcoming Earnings

Recursion Pharmaceuticals's next earnings date is estimated for March 3, 2027, based on past reporting schedules.

Q3 2026 Earnings Call Audio

MX:RXRX Q3 2026 Earnings Call
0:00 / 0:00

Q3 2026 Earnings Slide Deck

Q3 2026 Earnings Call Summary

Q3 2026
Earnings Call Date:Nov 02, 2026|% Change Since:-19.43%|
Earnings Call Sentiment|Positive

The call was strongly positive, led by encouraging early clinical activity for REC-4881 and REC-1245, progress across Sanofi, Roche, and Genentech partnerships, more than $535 million in partner cash inflows, substantial platform productivity gains, a $200 million financing, and runway into 2029. The main negatives were treatment-related adverse events, dose-limiting toxicities at higher REC-1245 doses, the early and investigational nature of the clinical data, and the need for further regulatory and registrational validation. Highlights significantly outweighed the lowlights.

Company Guidance

Recursion expects cash runway to extend into 2029; 2026 full-year cash operating expense guidance is less than $375 million, excluding partnership inflows and one-time expenses, and in 2027 cash operating expenses are expected to be less than $360 million. Sanofi’s optioned candidate is expected to begin phase I in 2027, with potential for additional partner milestones in 2027; for REC-4881, the company is targeting initiation of a registrational study in the second half of 2027, based on regulatory alignment, and expects to update FDA conversations and generate additional phase II data; for REC-1245, preliminary data from the endometrial expansion cohort are expected in the second half of 2027, along with additional clinical readouts from the rest of the portfolio.

  • Positive Clinical Data for REC-4881 in FAPIn the TUPELO study, 13 of 15 evaluable patients, or 87%, had a reduction in total polyp burden after 12 weeks of treatment. About one in three patients had a greater than or equal to 65% reduction in total polyp burden in 12 weeks.
  • Durable REC-4881 Response After Treatment CessationAfter approximately 12 weeks off treatment, about 85% of patients still had a lower total polyp burden than at baseline. In the upper GI tract, 11 of 12 evaluable patients, or about 92%, remained below baseline after 12 weeks off treatment.
  • REC-4881 Activity Across the GI TractREC-4881 reduced polyp burden in both the upper and lower GI tract, with median reductions of about 55% and 50%, respectively. After 12 weeks of treatment, 92% of evaluable patients had a reduction in upper GI polyp burden, while 82% had a reduction in lower GI polyp burden.
  • Reduction in Larger High-Risk PolypsAmong eight patients with polyps larger than 5 mm at baseline, six had fewer such polyps at week 13 and four had reductions of at least 80%. Two patients each went from more than 90 larger polyps to one, and another went from five to none.
  • REC-4881 Improvements in Spigelman StageAt week 13, six of 12 evaluable patients, or about 50%, improved by at least one Spigelman stage. Four moved from stage 3 to 2, one moved from stage 4 to 2, and one moved from stage 2 to 0; four patients assessed at week 25 remained at least one stage below baseline.
  • Deep Individual REC-4881 ResponseOne patient experienced a 98% reduction in total polyp burden, from 1,344 millimeters to 32 millimeters after 12 weeks of treatment. Of 96 polyps larger than 5 mm at baseline, only one remained above that threshold.
  • REC-1245 Demonstrates Early Clinical ActivityIn heavily pretreated solid-tumor patients, REC-1245 produced three partial responses: two confirmed responses in endometrial cancer and one unconfirmed response in hepatocellular carcinoma. The confirmed endometrial cancer responses were reductions of 38.2% and 48.9%, while the unconfirmed HCC response was a 55.9% reduction.
  • REC-1245 Disease Control and Expansion Dose SelectedAt doses of 45 milligrams and above, 11 of 12 response-evaluable patients, or 91.7%, had disease control at eight weeks. The company selected 45 milligrams once daily for expansion, with no serious treatment-related adverse events or dose reductions reported at that dose.
  • Efficient REC-1245 Candidate DevelopmentThe company screened 204 compounds to achieve a development candidate in 18 months, compared with an industry benchmark of roughly 2,500 compounds over four years for small molecules.
  • Sanofi Optioned Potential First-in-Class Oral I&I CandidateSanofi optioned a potential first-in-class oral small molecule designed to inhibit two inflammatory-disease targets. Sanofi will lead and fund further development, with Phase I expected to begin in 2027. The option triggered a $10 million payment, bringing total upfront and milestone payments from Sanofi to $144 million.
  • Progress Across Roche and Genentech PartnershipsGenentech optioned the first unexplored neuroscience target from Recursion's proprietary biological maps, and small-molecule discovery is underway. With Roche in oncology, the company's biology engine identified a new mechanism for acting on a pathway long considered undruggable, with in vivo confirmation of activity on the intended pathway.
  • Significant Partnership Cash Inflows and MilestonesRecursion has received more than $535 million in cash inflows from partners. Since 2024, Roche and Sanofi partnerships have generated more than $100 million from nine progress-based milestones, including six milestones across five Sanofi programs. The partnered programs include more than $300 million in milestones each with high single to double-digit royalties, while Sanofi programs carry up to $343 million in potential milestones plus double-digit royalties on net sales.
  • AI Platform and Proprietary Data ScaleThe company's platform draws on more than 50 petabytes of proprietary multimodal biological data and connects biology, chemistry, and clinical development through a closed-loop learning system. The company stated that its platform has generated tangible proof points in discovery, molecule design, and clinical development.
  • Platform Productivity GainsRecursion is synthesizing 80%-90% fewer compounds across its portfolio relative to industry benchmarks. ClinAgent can screen thousands of trial sites in minutes, and clinical enrollment is running about 30%-60% faster than industry benchmarks.
  • Stronger Balance Sheet and Extended RunwayThe company completed an oversubscribed $200 million follow-on offering, with more than 90% of the financing coming from healthcare-dedicated specialists and mutual funds that did not previously own Recursion. Pro forma cash and equivalents were $749 million as of September 30, excluding the recent $10 million Sanofi milestone, and cash runway is expected to extend into 2029.
  • Lower Operating Expense Guidance2026 cash operating expense guidance was lowered from $390 million to less than $375 million, excluding partnership inflows and one-time expenses. The company expects 2027 cash operating expenses to be less than $360 million, with 2026 guidance representing a nearly 40% reduction from comparable 2024 pro forma expenses.
  • Capital Focus on Higher-Conviction ProgramsManagement stated that it is fully funding and accelerating REC-4881 and REC-1245 while concentrating capital on the highest-value operations. The company also plans to continue investing in its AI engine, partnerships, proprietary maps, and wholly owned programs.
  • Leadership and Pipeline CatalystsThe board unanimously appointed Fred Hassan as non-executive chair. Looking ahead, the company expects the Sanofi candidate to enter Phase I in 2027, additional partnership milestones in 2027, preliminary REC-1245 expansion data in the second half of 2027, additional clinical readouts, and, subject to regulatory alignment, initiation of a REC-4881 registrational study in the second half of 2027.

MX:RXRX Earnings History

MX:RXRX earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Mar 03, 20272026 (Q4)-3.79--3.91――
Nov 02, 20262026 (Q3)-4.07-4.09-6.738.89% (+2.60)
Aug 05, 20262026 (Q2)-4.46-4.65-7.6339.02% (+2.98)
May 06, 20262026 (Q1)-4.93-4.09-9.356.00% (+5.21)
Feb 25, 20262025 (Q4)-5.60-3.91-9.8660.38% (+5.95)
Nov 05, 20252025 (Q3)-7.01-6.70-6.32-5.88% (-0.37)
Aug 05, 20252025 (Q2)-6.57-7.63-7.44-2.50% (-0.19)
May 05, 20252025 (Q1)-9.60-9.30-7.26-28.21% (-2.05)
Feb 28, 20252024 (Q4)-7.65-9.86-7.81-26.19% (-2.05)
Nov 06, 20242024 (Q3)-6.19-6.32-820.93% (+1.67)

The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.

Beat Missed