Leerink Global Healthcare Conference 2025
Logotype for BeOne Medicines AG

BeOne Medicines (ONC) Leerink Global Healthcare Conference 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for BeOne Medicines AG

Leerink Global Healthcare Conference 2025 summary

9 Jul, 2026

Strategic and operational highlights

  • Achieved 73% product growth in 2024, with revenue guidance for 2025 set at $4.9–$5.3 billion.

  • Expanded international footprint, now with over 60% of revenue from US and Europe, and opened a biologics facility in New Jersey.

  • Announced plans to re-domicile to Switzerland and change name to BeOne Medicines, effective first half of 2025.

  • Achieved three consecutive quarters of non-GAAP operating income and two quarters of positive cash flow from operations.

  • Maintains triple listing in US, Hong Kong, and China, balancing growth investment with operating discipline.

Hematology franchise and Brukinza performance

  • Brukinza became the leading BTK inhibitor in the US, surpassing Calquence in total dollar sales in Q4.

  • Holds over 50% new patient start share in CLL, with approvals and launches expanding in the EU and globally.

  • Clinical preference driven by selectivity, potency, and strong head-to-head data versus ibrutinib.

  • Fixed duration regimens are a strategic focus, with promising early results for Sonro plus Xanu in all-comers populations.

  • Phase 3 Celestial study in treatment-naive CLL completed enrollment; MRD data expected in about one year.

Pipeline and innovation

  • 13 new molecular entities entered the clinic in 2024, with proof-of-concept readouts expected in 2025–2026.

  • BTK degrader program advancing to two randomized phase 3 studies in 2024, with additional combination studies planned.

  • CDK4 inhibitor program rapidly enrolling globally, aiming for front-line and second-line registrational studies.

  • Internal ADC portfolio progressing, with first clinical data for B7-H4 ADC to be shared at ASCO.

  • PRMT5 and MAT2A inhibitor programs advancing, with combination studies set to begin in Q3 2024.

  • EGFR degrader in early phase dose escalation, targeting broad resistance and initiating mutations.

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