| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 9.32B | 9.12B | 9.98B | 8.60B | 8.83B | 8.55B |
| Gross Profit | 4.35B | 4.31B | 4.56B | 4.05B | 4.20B | 3.95B |
| EBITDA | 728.55M | 667.55M | 857.00M | 1.53B | 1.68B | 1.28B |
| Net Income | 227.00M | 1.00M | 77.00M | 784.05M | 828.37M | 409.01M |
Balance Sheet | ||||||
| Total Assets | 21.61B | 19.91B | 19.43B | 100.00K | 15.98B | 15.86B |
| Cash, Cash Equivalents and Short-Term Investments | 1.39B | 1.19B | 933.39M | 100.00K | 36.45M | 34.47M |
| Total Debt | 5.69B | 4.85B | 4.55B | 309.02M | 284.28M | 298.78M |
| Total Liabilities | 12.79B | 11.74B | 10.78B | 22.86K | 8.55B | 9.04B |
| Stockholders Equity | 8.82B | 8.16B | 7.28B | 77.14K | 7.43B | 6.82B |
Cash Flow | ||||||
| Free Cash Flow | 316.00M | 60.00M | -242.64M | 760.23M | 855.75M | 720.86M |
| Operating Cash Flow | 950.00M | 656.00M | 325.31M | 1.17B | 1.24B | 1.03B |
| Investing Cash Flow | -662.00M | -740.00M | -551.77M | -410.68M | -631.76M | -514.36M |
| Financing Cash Flow | 322.00M | 242.00M | 1.24B | -734.45M | -600.67M | -513.42M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
80 Outperform | CHF204.56B | 17.23 | ― | 3.26% | 7.62% | -18.33% | |
75 Outperform | CHF31.22B | 34.38 | 4.82% | 0.44% | 0.39% | -12.46% | |
73 Outperform | CHF256.01B | 27.04 | 31.98% | 3.01% | 4.77% | -11.07% | |
71 Outperform | CHF35.46B | 48.97 | ― | 0.76% | 5.93% | 29.83% | |
63 Neutral | CHF3.24B | 20.40 | 15.79% | 0.52% | 0.77% | 16.70% | |
59 Neutral | $24.86B | 126.00 | 2.64% | 1.04% | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Sandoz has launched Wyost® and Jubbonti®, two denosumab biosimilars, in Europe to treat cancer-related bone disease and osteoporosis, expanding access to affordable treatment options for millions. This launch marks a significant step in Sandoz’s growth strategy, reinforcing its leadership in the biosimilars market and its commitment to oncology and immunology. The introduction of these biosimilars is expected to have a substantial impact on European healthcare systems by providing sustainable treatment options and addressing the high burden of cancer and osteoporosis in the region.
Sandoz has launched Afqlir® (aflibercept) in Europe, offering an affordable treatment for retinal diseases such as neovascular age-related macular degeneration. This launch is a significant step in Sandoz’s growth strategy, enhancing its presence in the USD 15 billion anti-VEGF market and reinforcing its commitment to providing accessible biologic medicines. The approval by the European Commission and the product’s efficacy and safety matching the reference medicine Eylea® highlight its potential impact on patient care and healthcare systems.
Sandoz has launched TYRUKO® (natalizumab-sztn), the first and only FDA-approved biosimilar for multiple sclerosis in the US, marking a significant step in making MS treatment more affordable. This launch is expected to drive growth for Sandoz and strengthen its position in the neurology market, as TYRUKO® is also available in 14 European countries. The drug is part of a broader strategy to lead in the biosimilars market, with Sandoz partnering with Labcorp to provide free testing for anti-JCV antibodies, enhancing patient access and safety.
Sandoz has signed a global license agreement with EirGenix Inc. to commercialize a biosimilar of pertuzumab, a key oncology medicine for HER2-positive breast cancer. This strategic move aims to strengthen Sandoz’s position in the oncology sector and expand access to affordable cancer treatments, potentially impacting the USD 4.1 billion reference medicine market and aligning with the company’s goal to capitalize on the projected USD 300 billion biosimilar market over the next decade.
Sandoz has announced a strategic agreement to acquire Just-Evotec Biologics EU SAS, enhancing its in-house biosimilar development and manufacturing capabilities. This acquisition aligns with Sandoz’s strategy to capitalize on the projected USD 300 billion biosimilar market over the next decade, providing the company with continuous manufacturing technology and securing control over its pipeline. The transaction, valued at approximately USD 350 million, includes an indefinite technology license and reconfigures the existing partnership model to align incentives through license fees and development-related expenses.
Sandoz reported strong sales growth for the first nine months of 2025, with net sales reaching USD 8,057 million, a 5% increase at constant currencies. The company’s biosimilars segment showed significant growth, representing over 30% of net sales for the first time. Sandoz also upgraded its full-year margin guidance, reflecting the successful execution of its strategic roadmap and the expansion of its biosimilar infrastructure. The company is well-positioned for future growth, with anticipated biosimilar launches and a focus on sustainable European supply amidst geopolitical challenges.
Sandoz has reached an agreement with Regeneron Pharmaceuticals to resolve all patent disputes related to its FDA-approved aflibercept biosimilar, Enzeevu™, clearing the way for its US launch by the end of 2026. This move is expected to bolster Sandoz’s position in the US ophthalmology market, expand its biosimilar portfolio, and enhance patient access to affordable medicines, thereby advancing its growth strategy and leadership in the industry.