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Sanofi (SAN) investor relations material
Sanofi Citi Annual Global Healthcare Conference 2025 summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic transformation and operational efficiency
Revenue increased from €33 billion to €45 billion since 2019, with workforce and manufacturing sites significantly reduced to drive modernization and efficiency.
Shifted focus to become an R&D-led pharma company, exiting consumer business and investing heavily in pipeline innovation.
Commercial execution remains strong, with near double-digit growth and standout performance from key products.
Ongoing portfolio pruning and divestments generate capital gains and support a more focused R&D approach.
Efficiency gains achieved through SKU reduction and maintaining flat G&A costs while increasing R&D investment.
Pipeline development and portfolio strategy
Mid-late stage pipeline includes 12 drugs, with expectations that 4-5 successes will drive EPS growth; failures may prompt more external deals.
Acknowledges being light in preclinical/phase I programs compared to peers, aiming to add 5-15 high-quality early-stage assets.
Blueprint acquisition underwrites top-line growth into the early 2030s, with opportunistic later-stage additions considered.
R&D spend increased to over €8 billion, with a commitment to maintain or slightly grow this level to replenish the pipeline.
Pruning of R&D projects focuses resources on high-value indications, especially in immunology.
Product performance and market dynamics
DUPIXENT continues robust growth, projected to reach €22 billion by 2030, with less than 15% biologic penetration in its market.
Amlitelimab expected to exceed €5 billion in peak sales, targeting both naive and post-DUPIXENT patients, with a unique Q12 dosing advantage.
Tolebrutinib targets non-relapsing secondary progressive MS, with a PDUFA date set and focus on perfecting REMS for long-term value.
Itepekimab faced mixed trial results, with COVID-related factors impacting outcomes; timing and payer leverage are key for market entry.
Lunsekimig advanced to phase III in COPD based on mechanistic rationale, independent of asthma results.
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