| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 56.37B | 51.72B | 46.66B | 43.46B | 43.97B | 49.90B |
| Gross Profit | 42.96B | 38.90B | 34.19B | 31.88B | 32.24B | 34.78B |
| EBITDA | 22.85B | 20.71B | 18.25B | 14.68B | 30.91B | 17.21B |
| Net Income | 14.39B | 11.94B | 14.85B | 6.96B | 24.02B | 8.07B |
Balance Sheet | ||||||
| Total Assets | 107.29B | 102.25B | 99.94B | 117.45B | 131.79B | 127.78B |
| Cash, Cash Equivalents and Short-Term Investments | 9.75B | 13.35B | 13.96B | 18.61B | 28.11B | 11.29B |
| Total Debt | 32.02B | 31.26B | 26.35B | 27.91B | 31.02B | 37.85B |
| Total Liabilities | 62.54B | 58.12B | 53.20B | 58.03B | 63.97B | 71.11B |
| Stockholders Equity | 44.33B | 44.05B | 46.67B | 59.34B | 67.66B | 56.60B |
Cash Flow | ||||||
| Free Cash Flow | 18.30B | 13.80B | 11.71B | 11.56B | 12.10B | 11.06B |
| Operating Cash Flow | 21.07B | 17.62B | 14.46B | 14.24B | 15.07B | 13.65B |
| Investing Cash Flow | -5.81B | -7.51B | 5.60B | 1.47B | 4.21B | -13.18B |
| Financing Cash Flow | -19.55B | -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 |
|---|---|---|---|---|---|---|---|
80 Outperform | CHF193.14B | 16.27 | ― | 3.35% | 7.62% | -18.33% | |
75 Outperform | $31.91B | 35.14 | 4.82% | 0.44% | 0.39% | -12.46% | |
74 Outperform | CHF211.66B | 23.41 | ― | 3.04% | 4.77% | -11.07% | |
73 Outperform | $246.07B | 25.95 | 31.98% | 3.16% | 4.77% | -11.07% | |
71 Outperform | CHF36.90B | 50.96 | ― | 0.73% | 5.93% | 29.83% | |
70 Outperform | CHF37.57B | 115.80 | ― | 0.09% | 6.22% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
The Pan Tumor Rollover Study, officially titled ‘Pan-Tumor Study for Long-term Treatment of Cancer Patients Who Have Participated in BMS Sponsored Trials Investigating Nivolumab and Other Cancer Therapies,’ aims to assess the long-term safety of nivolumab, both as a monotherapy and in combination with other cancer treatments, across various tumor types. This study is significant as it seeks to provide insights into the sustained safety profile of these therapies, potentially impacting treatment protocols for cancer patients.
Novartis AG and Incyte Corporation have recently updated their clinical study on the JAK inhibitor ruxolitinib, targeting patients with various forms of myelofibrosis. Officially titled ‘A Phase Ib, Open-label, Dose-finding Study of the JAK Inhibitor INC424 Tablets,’ the study aims to determine the maximum safe starting dose of ruxolitinib in patients with specific platelet counts. This study is significant as it seeks to improve treatment options for myelofibrosis, a challenging bone marrow disorder.