Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
18.47M | 7.53M | 94.59M | 70.43M | 55.83M | Gross Profit |
18.47M | -322.59M | -146.22M | -89.51M | -41.12M | EBIT |
-536.25M | -496.20M | -324.20M | -186.31M | -93.94M | EBITDA |
-493.48M | -456.68M | -329.40M | -176.34M | -86.78M | Net Income Common Stockholders |
-589.53M | -526.24M | -402.55M | -242.37M | -164.13M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
1.08B | 614.82M | 782.58M | 471.64M | 464.06M | Total Assets |
1.40B | 824.32M | 1.01B | 841.32M | 533.80M | Total Debt |
695.45M | 755.77M | 749.34M | 269.93M | 138.94M | Net Debt |
600.59M | 642.75M | 683.76M | 157.26M | 55.95M | Total Liabilities |
1.54B | 1.21B | 1.12B | 597.46M | 420.42M | Stockholders Equity |
-135.37M | -386.32M | -107.90M | 243.86M | 113.38M |
Cash Flow | Free Cash Flow | |||
-399.80M | -415.75M | -310.85M | -191.39M | -2.11M | Operating Cash Flow |
-395.89M | -414.33M | -299.52M | -142.52M | 8.94M | Investing Cash Flow |
-553.10M | 239.25M | -262.13M | -147.78M | -196.51M | Financing Cash Flow |
930.61M | 221.32M | 516.17M | 319.98M | 234.12M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
78 Outperform | $13.46B | 32.10 | 8.05% | ― | 17.35% | 151.40% | |
69 Neutral | $9.68B | 41.27 | 19.71% | ― | 52.97% | ― | |
64 Neutral | $127.22B | ― | -3.15% | ― | 11.64% | -114.72% | |
49 Neutral | $5.31B | ― | -93.03% | ― | -10.48% | -18.79% | |
49 Neutral | $6.84B | 0.05 | -53.14% | 2.48% | 24.49% | -3.26% | |
49 Neutral | $30.91B | ― | -414.62% | ― | 22.97% | 38.54% | |
45 Neutral | $5.26B | ― | 435.49% | ― | 145.34% | 3.20% |
Cytokinetics has completed its midcycle review with the FDA regarding its new drug application for aficamten, aimed at treating obstructive hypertrophic cardiomyopathy. The FDA has indicated that it does not plan to hold an advisory committee meeting for this application, and a Late Cycle meeting is expected in June 2025. The company anticipates a differentiated label and risk mitigation profile for aficamten if approved, although detailed updates on FDA communications will not be shared.
On February 10, 2025, Cytokinetics, Incorporated appointed Robert E. Landry to its Board of Directors as a Class II member, with an initial term until the 2027 annual stockholders meeting. Landry was also appointed to the Audit Committee, and he will participate in the company’s non-employee director compensation arrangements, which include annual retainers and equity grants. This appointment aligns with Cytokinetics’ governance policies, as Landry is considered independent under relevant guidelines and requirements.