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BeOne Medicines (49BA) Q2 2026 Earnings Report

DE:49BA Q2 2026 EPS Results

Actual EPS
EUR 1.84
Consensus EPS
EUR 1.49
Beat/Miss
Beat by +EUR 0.35
One Year Ago EPS
EUR 0.81

DE:49BA Q2 2026 Revenue Results

Actual Revenue
EUR 1.53B
Expected Revenue
EUR 1.45B
Beat/Miss
Beat by +EUR 74.53M
YoY Revenue Growth
+29.39%

Earnings Announcement Details

Quarter
Q2 2026
Date
08/05/2026
Time
Before Open
Conference Call
Wednesday, August 5, 2026
DE:49BA Upcoming Earnings

BeOne Medicines's next earnings date is estimated for November 6, 2026, based on past reporting schedules.

Q2 2026 Earnings Call Audio

DE:49BA Q2 2026 Earnings Call
0:00 / 0:00

Q2 2026 Earnings Slide Deck

Q2 2026 Earnings Call Summary

Q2 2026
Earnings Call Date:Aug 05, 2026|% Change Since:20.44%|
Earnings Call Sentiment|Positive

The call presented a strongly positive commercial and financial picture: robust revenue and EPS growth, raised full‑year guidance, doubled free cash flow, high gross margins, and multiple meaningful regulatory and late‑stage pipeline milestones (MANGROVE result, BEQALZI approval, BTK degrader progress). Headwinds and uncertainties were present but limited relative to the strength described — including a missed uMRD superiority in CELESTIAL‑301 (though PFS remains the primary endpoint), a $60 million tax settlement, increased operating expense guidance to fund pipeline investment, and ongoing competitive dynamics. On balance, the company emphasized durable demand for BRUKINSA, expanding global footprint, and an accelerating late‑stage pipeline, leading to an overall favorable outlook.

Company Guidance

Management raised 2026 guidance, increasing revenue by $300 million to a new range of $6.6–$6.8 billion and boosting GAAP operating income by $250 million to $1.0–$1.1 billion (non‑GAAP operating income now $1.7–$1.8 billion); they expect full‑year gross margin in the high‑80% range and set operating expenses at $4.8–$5.0 billion to fund commercial and pipeline investments (with 2027 OPEX growth expected roughly in line with the past two years). For context from Q2, they reported $1.7 billion revenue, $1.5 billion gross profit (just under 90% gross margin), $1.2 billion operating expenses, $325 million operating income, $237 million net income, GAAP EPS $2.05, adjusted operating income $503 million, adjusted net income $444 million, adjusted diluted EPS $3.84, and free cash flow of $435 million.

  • Strong Top-Line GrowthTotal revenue of $1.7 billion in Q2 2026, representing 30% year-over-year growth.
  • Material EPS ExpansionGAAP diluted earnings per ADS were $2.05, up 144% versus $0.84 a year ago; adjusted diluted EPS were $3.84 versus $2.25 prior year.
  • BRUKINSA Commercial MomentumBRUKINSA global revenues exceeded $1.2 billion in Q2, up 31% year-over-year; #1 BTK inhibitor in the U.S. and globally, treating >300,000 patients across 80+ markets and approved in five B-cell malignancy indications.
  • Raised Full-Year 2026 GuidanceRevenue guidance increased by $300 million to $6.6–$6.8 billion; GAAP operating income guidance increased by $250 million to $1.0–$1.1 billion (non-GAAP operating income $1.7–$1.8 billion).
  • Improving Adjusted ProfitabilityAdjusted income from operations rose to $503 million (>80% growth YoY); adjusted net income $444 million.
  • Strong Cash GenerationFree cash flow doubled year-over-year to $435 million in the quarter.
  • Broad Geographic GrowthU.S. revenue ~ $899 million (31% YoY); China ~ $500 million (17% YoY; FX added ~7% of reported growth); Europe ~ $208 million (37% YoY); Rest of World ~ $73 million (more than doubled).
  • High Gross Margins and ProfitabilityGross profit of $1.5 billion with gross margin just under 90%; income from operations grew to $325 million and net income was $237 million (includes tax audit settlement impact).
  • Regulatory and Pipeline MilestonesFDA approval of BEQALZI (first/only BCL-2 inhibitor in mantle cell lymphoma); MANGROVE Phase III positive for BRUKINSA chemo‑free regimen (ZR vs BR HR reported as 0.57); Tacabrutideg (BTK degrader) tracking toward potential accelerated approval submission in relapsed/refractory CLL by year‑end.
  • Commercial Portfolio DiversificationTEVIMBRA generated $229 million (18% YoY growth) and Amgen in‑licensed portfolio delivered $157 million (25% YoY growth).
  • Robust R&D Progress and Late-Stage StartsMultiple solid tumor programs advancing to registrational trials or Phase III (CDK4 inhibitor in Phase III, GPC3 x 4-1BB enrollment for China registration cohort, B7-H4 ADC planned for pivotal study in ovarian cancer before year-end).
  • Large Real-World Evidence Supporting BRUKINSAMedicare real-world analysis of >10,500 previously untreated CLL patients showed BRUKINSA associated with a 24% and 36% reduction in risk of death versus acalabrutinib and ibrutinib, respectively; study published in a peer-reviewed journal.
  • Manufacturing InvestmentAnnounced $300 million expansion of U.S. manufacturing site in Hopewell, New Jersey to support growth.

DE:49BA Earnings History

DE:49BA earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Nov 06, 20262026 (Q3)1.70-0.98――
Aug 05, 20262026 (Q2)1.491.840.81125.27% (+1.02)
May 06, 20262026 (Q1)0.871.750―
Feb 26, 20262025 (Q4)1.110.54-1.28141.96% (+1.82)
Nov 06, 20252025 (Q3)0.760.98-1.03194.78% (+2.01)
Aug 06, 20252025 (Q2)0.350.81-1.03179.13% (+1.84)
May 07, 20252025 (Q1)-0.510.00-2.16100.00% (+2.16)
Feb 27, 20252024 (Q4)-0.91-1.28-3.1659.49% (+1.88)
Nov 12, 20242024 (Q3)-1.00-1.031.8-157.21% (-2.83)
Aug 26, 20242024 (Q2)-1.96-1.03-3.2668.41% (+2.23)

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
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