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Cytokinetics (CYTK)
NASDAQ:CYTK
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Cytokinetics (CYTK) AI Stock Analysis

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CYTK

Cytokinetics

(NASDAQ:CYTK)

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Neutral 58 (OpenAI - 4o)
Rating:58Neutral
Price Target:
$69.00
▲(2.66% Upside)
Cytokinetics' stock score is primarily influenced by its challenging financial performance, which is a major concern due to negative profitability and high leverage. However, strong technical indicators and positive earnings call sentiment regarding upcoming drug approvals provide some optimism. The valuation remains risky due to the lack of profitability and dividend yield.
Positive Factors
Strong Financial Position
A robust cash position provides Cytokinetics with the financial flexibility to support ongoing R&D and commercialization efforts, crucial for long-term growth.
European and Global Expansion Plans
Expanding into international markets can significantly increase Cytokinetics' revenue potential and market presence, supporting long-term growth.
MAPLE-HCM Trial Success
Successful trial results enhance the credibility and market potential of aficamten, positioning it as a strong alternative to existing therapies.
Negative Factors
Increased Net Loss
Rising net losses highlight financial challenges, potentially limiting resources for future development and impacting long-term sustainability.
Pending Regulatory Approval
Pending regulatory approvals introduce uncertainty, delaying market entry and revenue generation, which can affect strategic planning.
Financial Instability
High leverage and negative profitability can strain financial resources, limiting the company's ability to invest in growth and innovation.

Cytokinetics (CYTK) vs. SPDR S&P 500 ETF (SPY)

Cytokinetics Business Overview & Revenue Model

Company DescriptionCytokinetics, Inc. is a clinical-stage biopharmaceutical company focused on discovering, developing, and commercializing novel muscle activators and other therapeutics to treat debilitating diseases and medical conditions that affect muscle function. The company operates primarily in the sectors of neuromuscular diseases and cardiovascular diseases, with core products that include its lead drug candidates designed to enhance muscle contractility and improve overall muscle performance.
How the Company Makes MoneyCytokinetics generates revenue primarily through collaborations and partnerships with other pharmaceutical companies, as well as potential future sales of its drug candidates upon successful commercialization. The company engages in licensing agreements, where it may receive upfront payments, milestone payments based on clinical and regulatory progress, and royalties on future product sales. Additionally, Cytokinetics may also secure funding through grants or government programs aimed at supporting innovative research in the biopharmaceutical sector. The company's partnerships with larger pharmaceutical firms can also provide significant financial support and resources, enhancing its ability to advance its drug candidates through the development pipeline.

Cytokinetics Key Performance Indicators (KPIs)

Any
Any
Revenue by Segment
Revenue by Segment
Highlights revenue contributions from different business segments, providing insight into which areas drive growth and how diversified the company’s income streams are.
Chart InsightsCytokinetics' revenue is heavily reliant on sporadic license and milestone payments, with no consistent revenue stream from other segments. The recent earnings call highlights a strong financial position with $1.1 billion in cash, but increased R&D and administrative expenses are impacting profitability. The early completion of the ACACIA-HCM trial enrollment is a positive sign, yet the PDUFA date extension for aficamten could delay revenue from this key drug. Investors should watch for developments in the Sanofi partnership in China, which could open new revenue opportunities.
Data provided by:Main Street Data

Cytokinetics Earnings Call Summary

Earnings Call Date:Nov 05, 2025
(Q3-2025)
|
% Change Since: |
Next Earnings Date:Mar 04, 2026
Earnings Call Sentiment Neutral
The earnings call highlighted significant progress towards the approval and commercial readiness of aficamten, supported by strong clinical trial results and a solid financial position. However, increased net loss and pending regulatory approvals present challenges.
Q3-2025 Updates
Positive Updates
Progress Towards FDA Approval of Aficamten
Cytokinetics made significant progress in preparing for the potential FDA approval of aficamten for patients with oHCM, with constructive engagements with the FDA and completion of key commercial launch readiness activities.
MAPLE-HCM Trial Success
The MAPLE-HCM trial demonstrated the superiority of aficamten over metoprolol in patients with oHCM, showing significant improvements in exercise capacity and challenging the use of beta blockers as the standard-of-care therapy.
Strong Financial Position
Cytokinetics has a strong balance sheet with approximately $1.25 billion in cash and investments, bolstered by a convertible note offering that provides additional capital and financial flexibility.
European and Global Expansion Plans
Preparations for potential commercial launch of aficamten in the EU and coordination with Sanofi for potential approval in China are well underway, with expected EMA approval in the first half of 2026.
Negative Updates
Increased Net Loss
The net loss for the third quarter of 2025 was $306.2 million, a significant increase from the net loss of $160.5 million for the same period in 2024, driven by a debt conversion expense.
Pending Regulatory Approval and Market Uncertainties
While progress has been made, aficamten's approval by the FDA and EMA is still pending, with uncertainties around the finalization of the REMS program and potential market penetration.
Company Guidance
The guidance provided during the Cytokinetics Q3 2025 earnings call was comprehensive, focusing on the anticipated FDA approval of aficamten for obstructive hypertrophic cardiomyopathy (oHCM) by the end of 2025. Key metrics discussed included the completion of GCP inspections with no observations noted and the absence of pre-approval inspection notifications from the FDA. The company is preparing for a commercial launch with a newly onboarded cardiovascular sales team averaging over 20 years of industry experience, aiming to reach nearly 80% of the estimated 650 HCM prescribing healthcare providers within the first few weeks of January 2026. The metrics for measuring launch success include healthcare provider (HCP) prescribing breadth and depth, and the volume of patients on aficamten, with a goal to achieve parity access by the second half of 2026. Additionally, they expect potential European approval in the first half of 2026, with a launch in Germany planned for the same period, and efforts are ongoing with Sanofi for potential approval in China. Financially, the company reported a net loss of $306.2 million for Q3 2025, with cash and investments totaling $1.25 billion, bolstered by a convertible note offering.

Cytokinetics Financial Statement Overview

Summary
Cytokinetics faces significant financial challenges, with negative profitability and high leverage. Despite revenue growth, the company struggles with high costs and negative cash flows, indicating financial instability.
Income Statement
15
Very Negative
Cytokinetics has experienced significant revenue growth in recent periods, but it remains unprofitable with negative margins across the board. The gross profit margin and net profit margin are deeply negative, indicating high costs relative to revenue. The EBIT and EBITDA margins are also negative, reflecting ongoing operational challenges.
Balance Sheet
10
Very Negative
The balance sheet shows a concerning level of leverage, with a negative debt-to-equity ratio due to negative stockholders' equity. This indicates financial instability and potential risk in meeting debt obligations. The return on equity is positive but misleading due to negative equity, and the equity ratio is not favorable.
Cash Flow
20
Very Negative
Cytokinetics has negative operating and free cash flows, although there is some growth in free cash flow. The operating cash flow to net income ratio is negative, indicating cash flow challenges. The free cash flow to net income ratio is slightly positive, suggesting some alignment between cash flow and reported earnings.
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue87.21M18.47M7.53M94.59M70.43M55.83M
Gross Profit-111.22M-320.93M-322.59M-146.22M-89.51M-41.12M
EBITDA-646.17M-493.48M-456.68M-329.40M-176.34M-86.78M
Net Income-751.94M-589.53M-526.24M-388.95M-215.31M-127.29M
Balance Sheet
Total Assets1.44B1.40B824.32M1.01B841.32M533.80M
Cash, Cash Equivalents and Short-Term Investments962.53M1.08B614.82M782.58M471.64M464.06M
Total Debt1.20B788.68M755.77M750.30M269.93M138.94M
Total Liabilities1.96B1.54B1.21B1.12B597.46M420.42M
Stockholders Equity-521.12M-135.37M-386.32M-107.90M243.86M113.38M
Cash Flow
Free Cash Flow-453.38M-399.80M-415.75M-310.85M-191.39M-2.11M
Operating Cash Flow-432.93M-395.89M-414.33M-299.52M-142.52M8.94M
Investing Cash Flow198.72M-553.10M239.25M-262.13M-147.78M-196.51M
Financing Cash Flow416.14M930.61M221.32M516.17M319.98M234.12M

Cytokinetics Technical Analysis

Technical Analysis Sentiment
Positive
Last Price67.21
Price Trends
50DMA
59.09
Positive
100DMA
49.57
Positive
200DMA
43.84
Positive
Market Momentum
MACD
2.26
Negative
RSI
64.48
Neutral
STOCH
78.79
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For CYTK, the sentiment is Positive. The current price of 67.21 is above the 20-day moving average (MA) of 63.77, above the 50-day MA of 59.09, and above the 200-day MA of 43.84, indicating a bullish trend. The MACD of 2.26 indicates Negative momentum. The RSI at 64.48 is Neutral, neither overbought nor oversold. The STOCH value of 78.79 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for CYTK.

Cytokinetics Risk Analysis

Cytokinetics disclosed 37 risk factors in its most recent earnings report. Cytokinetics reported the most risks in the "Finance & Corporate" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Cytokinetics Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
58
Neutral
$8.22B2609.26%-17.08%
56
Neutral
$10.73B-32.44%106.27%-43.90%
55
Neutral
$7.62B-275.50%65.83%28.50%
52
Neutral
$7.11B-240.36%54.92%28.47%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
47
Neutral
$5.01B-22.60%74.91%31.54%
43
Neutral
$7.96B-38.79%-52.84%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
CYTK
Cytokinetics
67.55
15.53
29.85%
AXSM
Axsome Therapeutics
150.36
53.33
54.96%
RYTM
Rhythm Pharmaceuticals
108.75
46.80
75.54%
LEGN
Legend Biotech
28.19
-14.39
-33.80%
RNA
Avidity Biosciences
71.55
27.75
63.36%
NUVL
Nuvalent
109.86
13.56
14.08%

Cytokinetics Corporate Events

Cytokinetics’ Earnings Call: Progress and Challenges
Nov 7, 2025

Cytokinetics’ recent earnings call conveyed a mixed sentiment, highlighting both significant achievements and challenges. The company is making notable strides towards the approval and commercial readiness of aficamten, backed by impressive clinical trial outcomes and a robust financial standing. However, the increased net loss and pending regulatory approvals pose substantial hurdles.

Cytokinetics’ Q3 2025: Progress in Cardiac Therapies
Nov 6, 2025

Cytokinetics, Incorporated is a biopharmaceutical company specializing in cardiovascular treatments, focusing on muscle biology to develop potential new medicines for cardiac muscle dysfunction. In its third-quarter 2025 earnings report, Cytokinetics highlighted its ongoing preparations for the potential commercialization of aficamten, a cardiac myosin inhibitor, with regulatory reviews progressing in the U.S., China, and the EU. The company reported $1.25 billion in cash and investments, a significant increase from the previous quarter, and continued its strategic focus on advancing its cardiac muscle programs.

Private Placements and FinancingProduct-Related AnnouncementsRegulatory Filings and Compliance
Cytokinetics Discusses Aficamten with FDA in Late Cycle Meeting
Neutral
Sep 16, 2025

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.

Cytokinetics’ COMET-HF Study: A Potential Game-Changer for Heart Failure Treatment?
Sep 7, 2025

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.

Cytokinetics’ Aficamten Study: A Potential Breakthrough for Pediatric Heart Conditions
Sep 7, 2025

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.

Business Operations and StrategyProduct-Related Announcements
Cytokinetics Highlights Aficamten Data at ESC Congress
Positive
Sep 3, 2025

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.

Business Operations and StrategyProduct-Related Announcements
Cytokinetics Reveals Promising MAPLE-HCM Trial Results
Positive
Sep 2, 2025

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.

Executive/Board Changes
Cytokinetics Appoints James M. Daly to Board
Neutral
Aug 20, 2025

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.

Cytokinetics’ Aficamten Study: A Potential Breakthrough for Pediatric Heart Health
Aug 14, 2025

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’ Earnings Call: Progress Amid Challenges
Aug 12, 2025

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.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Nov 12, 2025