Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 85.74M | 18.47M | 7.53M | 94.59M | 70.43M | 55.83M |
Gross Profit | -194.63M | -320.93M | -322.59M | -146.22M | -89.51M | -41.12M |
EBITDA | -504.83M | -493.48M | -456.68M | -329.40M | -176.34M | -86.78M |
Net Income | -606.31M | -589.53M | -526.24M | -388.95M | -215.31M | -127.29M |
Balance Sheet | ||||||
Total Assets | 1.23B | 1.40B | 824.32M | 1.01B | 841.32M | 533.80M |
Cash, Cash Equivalents and Short-Term Investments | 858.13M | 1.08B | 614.82M | 782.58M | 471.64M | 464.06M |
Total Debt | 858.06M | 788.68M | 755.77M | 749.34M | 269.93M | 138.94M |
Total Liabilities | 1.59B | 1.54B | 1.21B | 1.12B | 597.46M | 420.42M |
Stockholders Equity | -368.72M | -135.37M | -386.32M | -107.90M | 243.86M | 113.38M |
Cash Flow | ||||||
Free Cash Flow | -440.48M | -399.80M | -415.75M | -310.85M | -191.39M | -2.11M |
Operating Cash Flow | -426.92M | -395.89M | -414.33M | -299.52M | -142.52M | 8.94M |
Investing Cash Flow | 224.65M | -553.10M | 239.25M | -262.13M | -147.78M | -196.51M |
Financing Cash Flow | 89.10M | 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 |
---|---|---|---|---|---|---|---|
57 Neutral | $6.57B | ― | -280.68% | ― | 69.83% | 22.16% | |
55 Neutral | $7.46B | ― | -1334.54% | ― | 53.55% | 30.87% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $6.07B | ― | -29.71% | ― | 74.86% | -13.23% | |
49 Neutral | $7.10B | ― | ― | ― | 2635.74% | 4.66% | |
48 Neutral | $7.15B | ― | -37.76% | ― | 1.23% | -20.45% | |
43 Neutral | $7.06B | ― | -43.55% | ― | ― | -76.16% |
On September 15, 2025, Cytokinetics participated in a Late Cycle Meeting with the FDA regarding its New Drug Application for aficamten, aimed at treating obstructive hypertrophic cardiomyopathy. The company discussed its Risk Evaluation and Mitigation Strategies (REMS) and anticipates a differentiated label for aficamten, pending FDA approval by December 26, 2025. Additionally, Cytokinetics responded to the European Medicines Agency’s questions about aficamten’s potential EU approval. The company plans to draw $100 million from a loan agreement with Royalty Pharma by October 1, 2025, to support its development efforts.
The most recent analyst rating on (CYTK) stock is a Buy with a $82.00 price target. To see the full list of analyst forecasts on Cytokinetics stock, see the CYTK Stock Forecast page.
Study Overview: The COMET-HF study, officially titled A Multi-Center, Double-Blind, Randomized, Placebo-Controlled Trial to Assess Efficacy and Safety of Omecamtiv Mecarbil in Patients With Symptomatic Heart Failure With Severely Reduced Ejection Fraction, aims to evaluate whether the investigational drug omecamtiv mecarbil can reduce the risk of heart failure-related events such as hospitalization, transplantation, or death in patients with severely reduced ejection fraction.
Study Overview: Cytokinetics is conducting a study titled ‘A Phase 2/3 Multicenter, Randomized, Double-Blind, Placebo-Controlled and Open-Label Extension Trial to Evaluate the Efficacy and Safety of Aficamten in a Pediatric Population With Symptomatic Obstructive Hypertrophic Cardiomyopathy.’ The study aims to assess the efficacy and safety of aficamten in children with symptomatic obstructive hypertrophic cardiomyopathy (oHCM), a condition that affects heart muscle function. This research is significant as it targets a pediatric population, addressing a critical need for effective treatments in this demographic.
On August 31, 2025, Cytokinetics presented new data on aficamten at the European Society of Cardiology Congress 2025, highlighting its efficacy in improving cardiac structure and function compared to metoprolol in patients with hypertrophic cardiomyopathy (HCM). The data, published in the Journal of the American College of Cardiology and Heart Rhythm, also showed that aficamten has a low incidence of atrial fibrillation and maintains a consistent safety profile, reinforcing its potential as a treatment option under FDA review.
The most recent analyst rating on (CYTK) stock is a Hold with a $35.00 price target. To see the full list of analyst forecasts on Cytokinetics stock, see the CYTK Stock Forecast page.
Cytokinetics announced the results of its MAPLE-HCM trial, presented at the European Society of Cardiology Congress 2025, showing that aficamten outperformed the standard beta-blocker metoprolol in improving exercise capacity in patients with obstructive hypertrophic cardiomyopathy (oHCM). The trial results suggest a potential shift in treatment practices, as aficamten demonstrated superior efficacy across primary and secondary endpoints, including improved functional class and reduced symptom burden, compared to metoprolol. These findings could significantly impact the company’s market positioning and offer new treatment options for oHCM patients.
The most recent analyst rating on (CYTK) stock is a Buy with a $84.00 price target. To see the full list of analyst forecasts on Cytokinetics stock, see the CYTK Stock Forecast page.
On August 19, 2025, Cytokinetics appointed James M. Daly to its Board of Directors as a Class III member, with his term expiring in 2028. Mr. Daly, determined to be independent under corporate governance guidelines, will also serve on the Compliance Committee and participate in the company’s non-employee director compensation arrangements, including stock options and restricted stock units.
The most recent analyst rating on (CYTK) stock is a Hold with a $39.00 price target. To see the full list of analyst forecasts on Cytokinetics stock, see the CYTK Stock Forecast page.
Study Overview: Cytokinetics is conducting a study titled A Phase 2/3 Multicenter, Randomized, Double-Blind, Placebo-Controlled and Open-Label Extension Trial to Evaluate the Efficacy and Safety of Aficamten in a Pediatric Population With Symptomatic Obstructive Hypertrophic Cardiomyopathy. The study aims to assess the efficacy, safety, and pharmacokinetics of aficamten in children and adolescents with symptomatic obstructive hypertrophic cardiomyopathy (oHCM), a condition that can severely impact heart function. This trial is significant as it targets a pediatric population, potentially offering a new treatment avenue for young patients.
Cytokinetics’ recent earnings call presented a mixed sentiment, highlighting significant strides in regulatory achievements and commercial preparations, particularly for their lead drug, aficamten. The company expressed optimism about upcoming approvals and market launches, yet acknowledged the challenges posed by increased expenses, net losses, and an extended PDUFA date.
Cytokinetics, Incorporated is a biopharmaceutical company specializing in cardiovascular treatments, focusing on muscle biology to develop new medicines for cardiac muscle dysfunction. The company is advancing its pipeline with potential regulatory approvals and commercialization of aficamten, a cardiac myosin inhibitor, for obstructive hypertrophic cardiomyopathy (HCM).