Investor Update
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Roche (ROG) Investor Update summary

Event summary combining transcript, slides, and related documents.

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Investor Update summary

9 Jul, 2026

Strategic and Financial Highlights

  • Hematology portfolio delivered $2.1 billion (CHF 2.1bn) in Q1 2025 sales, up 14% YoY at CER, with strong growth in Hemlibra (+11%), Polivy (+42%), and Columvi (+138%).

  • Over 50,000 patients treated globally with Polivy in DLBCL; U.S. first line share exceeds 30% and peak sales potential is around $2 billion.

  • Pipeline includes 8+ NMEs with >CHF 3bn peak sales potential and 5 NMEs with CHF 2–3bn potential per asset.

  • Multiple regulatory milestones and clinical readouts expected in 2025, including approvals and pivotal trial results across oncology and hematology.

  • IR events and annual Pharma Day planned for 2025 to provide updates on key franchises and pipeline progress.

Malignant Hematology: NHL and DLBCL Updates

  • SUNMO Phase III: Lunsumio plus Polivy in second line DLBCL showed a 59% reduction in risk of progression or death versus R-GemOx, with median PFS of 11.5 vs. 3.8 months and a doubling of complete response rate.

  • STARGLO Phase III: Columvi plus GemOx in second line DLBCL delivered a 41% improvement in overall survival and a 63% improvement in PFS, with sustained benefit at two-year follow-up.

  • Polivy + R-GemOx (POLARGO) in relapsed/refractory DLBCL showed a 40% improvement in overall survival, with 5-year data confirming Polivy-R-CHP as standard of care in first line DLBCL.

  • Bispecifics Columvi and Lunsumio are expanding in third and second line settings, with combined second line DLBCL opportunity above $1 billion and ongoing regulatory filings.

  • Early data support Columvi + Polivy-R-CHP in first line DLBCL, with high response rates and manageable safety profile.

Malignant Hematology: Follicular Lymphoma (FL) and Other NHL

  • Lunsumio SC demonstrated durable, high response rates in third line and promising efficacy in first line high-tumor burden FL, with manageable safety.

  • Lunsumio + lenalidomide in first and second line FL shows high response rates and durable responses; Phase III MorningLyte and CELESTIMO readouts expected H2 2025.

  • Broad clinical program aims to bring Lunsumio and Columvi to earlier lines and more NHL subtypes.

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