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BeOne Medicines (49BA) Q3 2026 Earnings Report

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DE:49BA Q3 2026 EPS Results

Actual EPS
EUR 2.95
Consensus EPS
EUR 1.72
Beat/Miss
Beat by +EUR 1.22
One Year Ago EPS
EUR 0.99

DE:49BA Q3 2026 Revenue Results

Actual Revenue
EUR 1.72B
Expected Revenue
EUR 1.59B
Beat/Miss
Beat by +EUR 127.06M
YoY Revenue Growth
+33.99%

Earnings Announcement Details

Quarter
Q3 2026
Date
11/05/2026
Time
Before Open
Conference Call
Thursday, November 5, 2026
DE:49BA Upcoming Earnings

BeOne Medicines's next earnings date is estimated for March 31, 2027, based on past reporting schedules.

Q3 2026 Earnings Call Audio

DE:49BA Q3 2026 Earnings Call
0:00 / 0:00

Q3 2026 Earnings Slide Deck

Q3 2026 Earnings Call Summary

Q3 2026
Earnings Call Date:Nov 05, 2026|% Change Since:12.57%|
Earnings Call Sentiment|Positive

The call was strongly positive, characterized by 33% product revenue growth, substantially higher operating income and free cash flow, raised 2026 guidance, sustained BRUKINSA momentum, and broad progress across hematology and solid tumor programs. The main challenges were the approximately $50 million order-timing benefit, future revenue pressure from biosimilars and potential VBP inclusion, a statutory Medicare Part D headwind, a PHESGO impairment charge, a more modest pace of future margin expansion, and the delayed tacabrutideg filing. Highlights significantly outweighed lowlights.

Company Guidance

For 2026, BeOne Medicines raised and narrowed guidance to total revenue of $6.9 billion-$7 billion, gross margin in the high 80% range, operating expenses of $4.9 billion-$5 billion, GAAP operating income of $1.2 billion-$1.3 billion, and non-GAAP operating income of $1.9 billion-$2 billion; it expects a modest net pricing benefit in the U.S. for BRUKINSA for the balance of the year, while looking ahead to 2027, it expects relatively stable net pricing and a flat to modest headwind from the increase in Medicare Part D manufacturer liability, operating expenses growth to be at least consistent with where we have been over the past several years, operating income to continue to grow meaningfully, and the pace of margin expansion to be modest as compared to 2025 and 2026; the current expectation is that the income tax valuation allowance reversal will occur in the fourth quarter and result in a material tax benefit.

  • Strong Q3 Revenue Growth and ProfitabilityProduct revenue grew 33% year-over-year to approximately $1.9 billion, while total revenue increased to $1.9 billion from $1.4 billion in the prior year. Income from operations grew 157% to $419 million, net income was $385 million, and GAAP diluted earnings per ADS rose to $3.28 from $1.09.
  • Adjusted Earnings and Cash Flow ExpansionAdjusted operating income increased more than 79% to $612 million, adjusted net income reached $539 million, and adjusted diluted earnings per ADS increased to $4.59 from $2.65. Free cash flow grew 34% year-over-year to $474 million.
  • BRUKINSA Reached $1.4 Billion in Quarterly SalesBRUKINSA global sales totaled approximately $1.4 billion, growing 34% year-over-year, with growth in all regions. U.S. sales exceeded $1 billion for the first time and grew 36%.
  • Broad Drivers of BRUKINSA DemandBRUKINSA growth was supported by sustained high levels of new patient starts, growth across all approved indications, improved patient adherence, longer treatment duration, and continued strength in indications beyond CLL, particularly Waldenstrom's.
  • BRUKINSA Real-World Evidence Continued to Favor the ProductAcross six independent real-world data sets covering overall survival, time to discontinuation, and time to next treatment, all 21 hazard ratios favored BRUKINSA. Versus acalabrutinib, four large U.S. claims data sets showed a 16%-25% lower risk of death, while versus ibrutinib the reduction was 27%-36%.
  • TEVIMBRA and the Broader Commercial Portfolio GrewTEVIMBRA generated approximately $243 million in revenue, up 28% year-over-year, with continued leadership in China and increasing contributions from other markets. The Amgen in-license portfolio generated approximately $167 million, up 26%, and the HERIZON regimen received encouraging early prescriber reception following its August U.S. approval and launch.
  • Growth Was Broad-Based Across RegionsChina contributed approximately $527 million, growing 21% in the seasonally high third quarter, with continued leadership for TEVIMBRA and BRUKINSA and contributions from BEQALZI and ZIIHERA. Europe generated approximately $234 million, up 41%, while rest-of-world markets contributed approximately $80 million, up 58%, with Japan and Brazil becoming increasingly meaningful.
  • Raised and Narrowed 2026 Financial GuidanceThe company raised and narrowed its 2026 total revenue outlook to $6.9 billion-$7 billion from $6.6 billion-$6.8 billion. GAAP operating income guidance increased by $200 million across the range to $1.2 billion-$1.3 billion, and non-GAAP operating income guidance increased by $200 million to $1.9 billion-$2 billion.
  • Expected Tax Benefit from Valuation Allowance ReversalThe company expects a portion of its deferred tax assets to be recognized in the fourth quarter, resulting in a material tax benefit to the income tax provision and correspondingly to full-year GAAP net income.
  • Strong Pipeline Productivity in Solid TumorsThe company has shared differentiated data for five solid tumor programs: a GPC3 x 4-1BB bispecific antibody, a brain-penetrant PRMT5 inhibitor, a CEA ADC, a CDK4 inhibitor, and a B7-H4 ADC. All five are advancing toward registration-enabling development.
  • Rapid Advancement of Late-Stage ProgramsThe CDK4 inhibitor and B7-H4 ADC moved from first-in-human studies to pivotal development in two and a half years. The B7-H4 ADC achieved first subject enrollment in the Starstone-301 phase III study, the second solid tumor phase III start of the year, while the CDK4 inhibitor KANDELA-302 is being upsized to accelerate the readout.
  • Positive GPC3 x 4-1BB HCC DataIn heavily pretreated second-line-plus hepatocellular carcinoma, BGB-B2033 monotherapy demonstrated a 36% confirmed response rate, with a six-month duration-of-response rate of approximately 79%, strong durability, and a favorable safety profile without cytokine release syndrome. The potential pivotal third-line-plus China and Korea cohort is fully enrolled.
  • GPC3 x 4-1BB Development ExpansionThe company plans to initiate a second-line-plus single-arm study before year-end to support a potential U.S. accelerated approval pathway, a second-line-plus phase III confirmatory trial, and a global phase III first-line HCC study with TEVIMBRA and Avastin in the first half of 2027.
  • Encouraging PRMT5 Inhibitor ResultsThe brain-penetrant PRMT5 inhibitor produced a 38.5% confirmed response rate and median progression-free survival of 8.1 months in previously treated MTAP-deficient EGFR wild-type non-small cell lung cancer. The company also observed intracranial responses, including a 30.8% confirmed intracranial response rate in patients with active brain metastases and a 16% intracranial progression rate.
  • PRMT5 Development and Collaboration ExpansionThe company plans to evaluate PRMT5 combinations with RAS inhibitors from its Revolution Medicines collaboration in pancreatic cancer before year-end and is already evaluating combinations with PD-1 and chemotherapy in first-line non-small cell lung cancer. Preclinical modeling showed no significant concern around potential drug-drug interaction with the Revolution Medicines assets, subject to clinical validation.
  • Strong Early CEA ADC ActivityThe CEA ADC produced a 60% confirmed response rate in heavily pretreated CEA non-small cell lung cancer, with a six-month duration-of-response rate of 73%. No grade 3 or higher interstitial lung disease or ocular events were observed in the presented phase I-A dataset, and the six-month PFS rate was 76.2% with median PFS not reached at the data cutoff.
  • Hematology Pipeline MilestonesFor BRUKINSA in treatment-naive mantle cell lymphoma, submissions were completed in the U.S., Europe, and China, and the FDA granted priority review. MANGROVE will be presented in an ASH plenary session. For BEQALZI, CELESTIAL-304 remains on track to complete enrollment before year-end.
  • Tacabrutideg Phase II Success and Program ExpansionThe phase II CaDAnCe-101 study in relapsed/refractory CLL met its primary overall response rate endpoint, with encouraging duration of response, progression-free survival, and safety. The company increased CaDAnCe-304 enrollment from 500 to 600 patients to accelerate the readout, remains on track to complete enrollment in early 2027, and plans to begin a phase III tacabrutideg-plus-sonrotoclax study in the first half of 2027.
  • Potential Tacabrutideg Indication ExpansionThe company is planning a potential FDA submission for tacabrutideg in mid-2027 and is on pace to initiate a chronic spontaneous urticaria trial in early 2027. Management stated that the broader opportunity extends beyond the accelerated approval setting, including head-to-head, combination, and future development programs.
  • Upcoming ASH Data and MCL OpportunityBeOne has 45 accepted ASH abstracts and five oral presentations across BRUKINSA, BEQALZI, and tacabrutideg. MANGROVE is described as the first and only chemo-free regimen in previously untreated mantle cell lymphoma to show superiority over a chemo regimen. The U.S. mantle cell lymphoma population is approximately 4,000 patients annually, with an additional opportunity in Europe and China.
  • KANDELA-302 Enrollment and Readout AccelerationThe phase III KANDELA-302 study is recruiting slightly ahead of internal projections. The study is being increased by approximately 10%, from a little over 1,000 patients to 1,200 patients, with management stating that the larger sample size increases statistical power and should bring the readout earlier without changing the overall event-rate assumptions.
  • Continued Investment in Innovation and InfrastructureManagement emphasized continued investment in the pipeline, commercial growth, and the company's global development superhighway. The company stated that it has brought more new oncology medicines into the clinic over the last three years than any other company in the industry and intends to continue investing with discipline to maximize patient impact and shareholder value.
  • Revolution Medicines Collaboration ExpandedBeOne is conducting the phase III RASonate 312 colorectal cancer study of RASONQUE in combination with standard care. The companies are also exploring combinations involving BeOne's PRMT5 inhibitor and EGFR x MET x MET trispecific antibody with Revolution Medicines assets, including zoldonrasib.

DE:49BA Earnings History

DE:49BA earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Mar 31, 20272026 (Q4)2.34-0.54――
Nov 05, 20262026 (Q3)1.722.950.99198.17% (+1.96)
Aug 05, 20262026 (Q2)1.511.860.83125.27% (+1.03)
May 06, 20262026 (Q1)0.881.780―
Feb 26, 20262025 (Q4)1.130.54-1.3141.96% (+1.84)
Nov 06, 20252025 (Q3)0.770.99-1.04194.78% (+2.03)
Aug 06, 20252025 (Q2)0.350.83-1.04179.13% (+1.87)
May 07, 20252025 (Q1)-0.520.00-2.19100.00% (+2.19)
Feb 27, 20252024 (Q4)-0.92-1.30-3.259.49% (+1.91)
Nov 12, 20242024 (Q3)-1.01-1.041.82-157.21% (-2.87)

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