| Breakdown | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 51.72B | 46.66B | 51.83B | 52.88B | 49.90B |
| Gross Profit | 38.90B | 34.19B | 36.34B | 37.01B | 34.78B |
| EBITDA | 20.71B | 18.29B | 14.73B | 17.13B | 15.24B |
| Net Income | 11.94B | 14.85B | 6.96B | 24.02B | 8.07B |
Balance Sheet | |||||
| Total Assets | 102.25B | 99.94B | 117.45B | 131.79B | 132.06B |
| Cash, Cash Equivalents and Short-Term Investments | 13.35B | 13.96B | 18.93B | 28.33B | 11.56B |
| Total Debt | 31.26B | 26.35B | 27.96B | 31.09B | 38.05B |
| Total Liabilities | 58.12B | 53.20B | 58.03B | 63.97B | 75.39B |
| Stockholders Equity | 44.05B | 46.67B | 59.34B | 67.66B | 56.60B |
Cash Flow | |||||
| Free Cash Flow | 13.80B | 11.71B | 11.56B | 12.10B | 11.06B |
| Operating Cash Flow | 17.62B | 14.46B | 14.24B | 15.07B | 13.65B |
| Investing Cash Flow | -7.51B | 5.60B | 1.47B | 4.21B | -13.18B |
| Financing Cash Flow | -11.74B | -14.28B | -20.56B | -16.26B | -2.21B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
78 Outperform | $250.07B | 18.94 | 32.82% | 3.06% | 12.38% | -12.67% | |
78 Outperform | $140.77B | 13.17 | 12.16% | 6.91% | 14.72% | ― | |
77 Outperform | $258.51B | 31.03 | 19.76% | 1.88% | 15.08% | 29.15% | |
76 Outperform | $217.76B | 13.44 | 35.44% | 3.70% | 2.00% | 20.01% | |
76 Outperform | $125.86B | 12.84 | 8.39% | 4.28% | -9.32% | 120.62% | |
64 Neutral | $403.22B | 108.62 | 112.90% | 2.88% | 6.05% | -29.75% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On September 30, 2025, Novartis announced that its drug Rhapsido® (remibrutinib) received FDA approval as the first oral Bruton’s tyrosine kinase inhibitor (BTKi) for treating chronic spontaneous urticaria (CSU) in adults who remain symptomatic despite antihistamine treatment. This approval marks a significant advancement in CSU care, offering a new oral treatment option that provides fast relief without the need for injections or lab monitoring. The approval is based on positive results from Phase III clinical trials, and it expands Novartis’s immunology portfolio, potentially impacting the lives of 1.7 million people in the US living with CSU.
On August 11, 2025, Novartis announced that its Phase III clinical trials for ianalumab, a novel treatment for Sjögren’s disease, successfully met their primary endpoints. The trials, NEPTUNUS-1 and NEPTUNUS-2, demonstrated statistically significant improvements in disease activity, positioning ianalumab as a potential first targeted treatment for this chronic autoimmune disease. The results are significant for Novartis as they plan to present the data at a medical congress and seek global health authority approvals, potentially enhancing their market position in autoimmune disease treatments.