Banco Santander announces third-quarter earnings
Q3 Financial Performance: Banco Santander reported a Q3 GAAP EPS of €0.23, with net interest income of €10.35 billion, reflecting a 2% year-over-year increase. Profit attributable to the parent reached €3,504 million, marking a sixth consecutive quarterly record.
CET1 Ratio and Profit Growth: The CET1 ratio stood at 13.1% at the end of September 2025, slightly above the target range. Year-to-date, attributable profit increased by 11% to €10,337 million, driven by strong performances across revenue lines and controlled costs.
Impact of Argentina: Despite challenges in Argentina, profit growth remained resilient, with a 4% increase when excluding its impact. The bank's solid net fee income and lower provisions contributed to overall profitability.
Future Outlook: Banco Santander's strong profit growth across global businesses positions it well to meet its 2025 targets, supported by a solid increase in revenue and flat costs in real terms.
Trade with 70% Backtested Accuracy
Analyst Views on SAN
About SAN
About the author

- Merger and Acquisition Activity: The year has seen significant merger and acquisition activity, with many deals nearing closure.
- Stock Performance: Stocks of companies being acquired are expected to rise upon the completion of these deals.

- Merger and Acquisition Activity: The year has seen significant merger and acquisition activity, with many deals nearing closure.
- Stock Performance: Stocks of companies involved in these acquisitions are expected to rise once the deals are finalized.
- Investigation Launched: Pomerantz LLP is investigating claims against Santander Bank and its executives for potential securities fraud and other unlawful business practices, aiming to protect investor rights and pursue legal accountability.
- Market Reaction: Following the collapse of UK mortgage provider Market Financial Solutions, Santander's American Depositary Shares (ADS) fell by 7.57% over two trading sessions, raising concerns about potential losses for the bank.
- Industry Impact: This incident has triggered warnings about broader risks in the private credit industry, undermining market confidence in Santander and potentially affecting its future financing capabilities and investor trust.
- Legal Context: Pomerantz LLP, a prominent securities class action law firm with over 85 years of history, is dedicated to advocating for victims of securities fraud, indicating that this case may lead to wider legal actions.

Partnership Announcement: Doral Renewables has been appointed as the lead arranger for a financing deal involving multiple partners including Santander, HSBC, and others.
Debt Providers Involved: The arrangement includes a syndicate of debt providers, indicating a collaborative effort to support renewable energy projects.
- Clinical Trial Results: Dupixent (dupilumab) has been approved in Japan for the treatment of moderate-to-severe bullous pemphigoid (BP), based on the LIBERTY-BP-ADEPT Phase 2/3 trial results, which showed that 18% of Dupixent patients achieved sustained disease remission at Week 36, significantly higher than the 4% in the placebo group (p=0.0250), indicating its potential to improve patient quality of life.
- Safety Analysis: In the Dupixent group, 26% of patients experienced treatment-related adverse events (AEs), compared to 15% in the placebo group, with conjunctivitis being the most common AE at 4%, highlighting the need for careful safety management in clinical applications.
- Market Expansion: This approval marks the seventh indication for Dupixent in Japan, where it is also approved for atopic dermatitis, asthma, and other conditions, demonstrating its broad market applicability and further solidifying Regeneron and Sanofi's leadership in the immunotherapy space.
- Innovative Treatment Regimen: Dupixent is administered via subcutaneous injection every two weeks, in conjunction with standard oral corticosteroid (OCS) therapy, effectively controlling BP symptoms, which is expected to provide patients with more flexible treatment options, enhancing adherence and therapeutic outcomes.
- Approval in Japan: Dupixent (dupilumab) has been granted marketing authorization by Japan's Ministry of Health, Labour and Welfare as the first targeted therapy for adults with moderate-to-severe bullous pemphigoid (BP), marking a significant advancement in the dermatology sector.
- Clinical Trial Results: In the LIBERTY-BP-ADEPT study, 18% of Dupixent patients achieved sustained remission at Week 36, compared to only 4% in the placebo group (p=0.0250), demonstrating its superior efficacy in treating BP.
- Safety Data: Among Dupixent patients, 26% reported treatment-related adverse events, with conjunctivitis being the most common at 4%, indicating a need for ongoing monitoring of the risk-benefit profile.
- Market Potential: This approval represents the seventh indication for Dupixent in Japan, which is expected to further enhance its acceptance in over 60 countries globally, strengthening the company's competitive position in the immunotherapy market.









