Cytokinetics Reports Third Quarter 2023 Financial Results
- Positive results from the SEQUOIA-HCM trial of aficamten in obstructive hypertrophic cardiomyopathy (HCM)
- Sustained improvements in clinical efficacy endpoints from the FOREST-HCM study of aficamten
- Initiation of enrollment in the ACACIA-HCM trial of aficamten in non-obstructive HCM
- Cash, cash equivalents, and investments totaling $554.7 million on September 30, 2023
- None.
On Track for Topline Results from SEQUOIA-HCM,
a Pivotal Phase 3 Clinical Trial of Aficamten in Obstructive HCM,
in Late December
Long-Term Data from FOREST-HCM,
the Open-Label Extension Study of Aficamten,
Show Sustained Improvements in Clinical Efficacy Endpoints
and No Treatment Interruptions for Low Ejection Fraction
Initiated Enrollment in ACACIA-HCM,
a Pivotal Phase 3 Clinical Trial of Aficamten in Non-Obstructive HCM
SOUTH SAN FRANCISCO, Calif., Nov. 02, 2023 (GLOBE NEWSWIRE) -- Cytokinetics, Incorporated (Nasdaq: CYTK) reported financial results for the third quarter of 2023. Net loss for the third quarter was
“During the third quarter we made considerable progress across our specialty cardiology franchise, with aficamten remaining our top priority. Of note, the baseline characteristics of patients enrolled in SEQUOIA-HCM met our objectives for the trial and align with our goal to assess aficamten as a potential next-in-class cardiac myosin inhibitor in a population with a substantial deficit in exercise capacity and significant symptom burden despite existing standard of care,” said Robert I. Blum, Cytokinetics’ President and Chief Executive Officer. “In addition, we recently shared longer-term data from FOREST-HCM that demonstrate durable reductions in pressure gradients and cardiac biomarkers as well as improved symptoms in patients with obstructive HCM. During the quarter we also started ACACIA-HCM, a pivotal Phase 3 clinical trial of aficamten in patients with non-obstructive HCM. Alongside these increasing commitments to aficamten, we are approaching the end of 2023 in a strong position with the resources and pipeline to execute on our goals in service to both patients and shareholders.”
Q3 and Recent Highlights
Cardiac Muscle Programs
aficamten (cardiac myosin inhibitor)
- Presented baseline characteristics from SEQUOIA-HCM (Safety, Efficacy, and Quantitative Understanding of Obstruction Impact of Aficamten in HCM), the pivotal Phase 3 trial of aficamten in obstructive hypertrophic cardiomyopathy (HCM), at the HCM Society Scientific Sessions 2023.
- Shared new long-term data from FOREST-HCM (Follow-up, Open-Label, Research Evaluation of Sustained Treatment with Aficamten in HCM) the open-label extension clinical study of aficamten in patients with HCM, at the Company’s recent Investor and Analyst Day, demonstrating sustained reductions in left ventricular outflow tract (LVOT) gradients with no treatment interruptions for low left ventricular ejection fraction (LVEF) due to aficamten. Additionally, patients experienced sustained reductions in cardiac biomarkers and improved symptoms. Aficamten has been generally well-tolerated, with no treatment-related serious adverse events (SAEs) as assessed by investigators, and no patient deaths.
- Announced the start of ACACIA-HCM (Assessment Comparing Aficamten to Placebo on Cardiac Endpoints In Adults with Non-Obstructive HCM), a pivotal Phase 3 clinical trial of aficamten in patients with non-obstructive HCM.
- Published a manuscript entitled “Aficamten in Patients with Drug-Refractory Obstructive Hypertrophic Cardiomyopathy Receiving Disopyramide: REDWOOD-HCM Cohort 3 Analysis” in the Journal of Cardiac Failure.
- Published a manuscript entitled “Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Doses of Aficamten in Healthy Chinese Participants: a Randomized, Double-blind, Placebo-controlled, Phase 1 Study” in the Frontiers of Pharmacology.
- Published a manuscript entitled “Exercise Capacity in Patients With Obstructive Hypertrophic Cardiomyopathy: SEQUOIA-HCM Baseline Characteristics and Study Design” in the Journal of the American College of Cardiology: Heart Failure.
omecamtiv mecarbil (cardiac myosin activator)
- Submitted a Formal Dispute Resolution Request to the Office of New Drugs (OND) of the U.S. Food and Drug Administration (FDA) regarding the Complete Response Letter (CRL) for omecamtiv mecarbil with objective to appeal the FDA’s conclusion, as stated in the CRL, that substantial evidence of effectiveness had not been established to support approval of omecamtiv mecarbil.
- Submitted responses to the Day 120 questions to the European Medicines Agency (EMA) in connection with its review of the marketing application for omecamtiv mecarbil for the treatment of advanced or worsening heart failure with reduced ejection fraction (HFrEF).
- Ji Xing Pharmaceuticals submitted a request for voluntary withdrawal of the NDA for omecamtiv mecarbil to the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of the People’s Republic of China, subject to potential re-submission upon receipt of favorable feedback from EMA or FDA with regard to potential drug approval for omecamtiv mecarbil in the EU or U.S., respectively.
CK-3828136 (CK-136, cardiac troponin activator)
- Completed the single ascending dose (SAD) cohorts of the Phase 1 study of CK-136 in healthy participants. Initiated analyses of the SAD data to inform potentially proceeding to the multiple ascending dose (MAD) cohorts of the Phase 1 study.
CK-4021586 (CK-586, cardiac myosin inhibitor)
- Completed the SAD cohorts of the Phase 1 study of CK-586 in healthy participants. Completed analyses of the SAD data which are supportive of proceeding to the MAD cohorts of the Phase 1 study in Q4 2023.
Pre-Clinical Development and Ongoing Research
- Continued research activities directed to our other muscle biology research programs.
Corporate
- Announced a call for proposals for the sixth annual Cytokinetics Communications Grant Program. The program awards five grants worth
$20,000 each to patient advocacy organizations serving the HCM, heart failure or ALS communities, and is intended to support increased capacity in communications and outreach.
Upcoming Corporate Milestones
Cardiac Muscle Programs
aficamten (cardiac myosin inhibitor)
- Expect topline results from SEQUOIA-HCM in late December.
- Continue enrollment of MAPLE-HCM.
- Continue enrollment of ACACIA-HCM.
- Continue advancing go-to-market strategy for aficamten.
omecamtiv mecarbil (cardiac myosin activator)
- Continue to pursue potential approval for omecamtiv mecarbil in Europe.
CK-3828136 (CK-136, cardiac troponin activator)
- Analyze SAD data from the Phase 1 study of CK-136 to inform potentially proceeding with the MAD cohorts in the Phase 1 study.
CK-4021586 (CK-586, cardiac myosin inhibitor)
- Proceed to the MAD cohorts in the Phase 1 study of CK-586.
Financials
Revenues for the three and nine months ended September 30, 2023 were
Research and development expenses for the three and nine months ended September 30, 2023 increased to
General and administrative expenses for the three months ended September 30, 2023 decreased to
During the quarter we also received a
Conference Call and Webcast Information
Members of Cytokinetics’ senior management team will review the company’s third quarter 2023 results on a conference call today at 4:30 PM Eastern Time. The conference call will be simultaneously webcast and can be accessed from the Investors & Media section of Cytokinetics’ website at www.cytokinetics.com. The live audio of the conference call can also be accessed by telephone by registering in advance at the following link: Cytokinetics Q3 2023 Earnings Conference Call. Upon registration, participants will receive a dial-in number and a unique passcode to access the call. An archived replay of the webcast will be available via Cytokinetics’ website for twelve months.
About Cytokinetics
Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Aficamten is a next-in-class cardiac myosin inhibitor, currently the subject of three Phase 3 clinical trials: SEQUOIA-HCM, evaluating aficamten in patients with obstructive hypertrophic cardiomyopathy (HCM), MAPLE-HCM, evaluating aficamten as monotherapy compared to metoprolol as monotherapy in patients with obstructive HCM and ACACIA-HCM, evaluating aficamten in patients with non-obstructive HCM. Cytokinetics is also developing omecamtiv mecarbil, a cardiac muscle activator, in patients with heart failure. Additionally, Cytokinetics is developing CK-136, a cardiac troponin activator for the potential treatment HFrEF and other types of heart failure, such as right ventricular failure, resulting from impaired cardiac contractility, and CK-586, a cardiac myosin inhibitor with a mechanism of action distinct from aficamten for the potential treatment of HFpEF. In 2023, Cytokinetics is celebrating its 25-year history of pioneering innovation in muscle biology and related pharmacology focused to diseases of muscle dysfunction and conditions of muscle weakness.
For additional information about Cytokinetics, visit www.cytokinetics.com and follow us on X, LinkedIn, Facebook and YouTube.
Forward-Looking Statements
This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the “Act”). Cytokinetics claims the protection of the Act’s Safe Harbor for forward-looking statements. Examples of such statements include, but not limited to, statements, express or implied, relating to our or our partners’ research and development and commercial readiness activities, including the initiation, conduct, design, enrollment, progress, continuation, completion, timing and results of any of our clinical trials, or more specifically, our ability to obtain approval of our marketing authorisation application for omecamtiv mecarbil in the E.U., our ability to publish topline results of SEQUOIA-HCM by the end of 2023, the timing of interactions with FDA or any other regulatory authorities in connection to any of our drug candidates and the outcomes of such interactions; statements regarding the potential outcome of our Formal Dispute Resolution Request to FDA regarding the Complete Response Letter (CRL) for omecamtiv mecarbil, statements relating to the potential patient population who could benefit from omecamtiv mecarbil, aficamten, CK-136, CK-586 or any of our other drug candidates; statements relating to our ability to receive additional capital or other funding, including, but not limited to, our ability to meet any of the conditions relating to or to otherwise secure additional loan disbursements under any of our agreements with entities affiliated with Royalty Pharma or additional milestone payments from Ji Xing; statements relating to our operating expenses or cash utilization for the remainder of 2023, and statements relating to our cash balance at year-end 2023 or any other particular date or the amount of cash runway such cash balances represent at any particular time. Such statements are based on management's current expectations, but actual results may differ materially due to various risks and uncertainties, including, but not limited to Cytokinetics’ need for additional funding and such additional funding may not be available on acceptable terms, if at all; potential difficulties or delays in the development, testing, regulatory approvals for trial commencement, progression or product sale or manufacturing, or production of Cytokinetics’ drug candidates that could slow or prevent clinical development or product approval; patient enrollment for or conduct of clinical trials may be difficult or delayed; the FDA or foreign regulatory agencies may delay or limit Cytokinetics’ or its partners’ ability to conduct clinical trials; Cytokinetics may incur unanticipated research and development and other costs; standards of care may change, rendering Cytokinetics’ drug candidates obsolete; and competitive products or alternative therapies may be developed by others for the treatment of indications Cytokinetics’ drug candidates and potential drug candidates may target. For further information regarding these and other risks related to Cytokinetics’ business, investors should consult Cytokinetics’ filings with the Securities and Exchange Commission, particularly under the caption “Risk Factors” in Cytokinetics’ Annual Report on Form 10-K for the year 2022. Forward-looking statements are not guarantees of future performance, and Cytokinetics’ actual results of operations, financial condition and liquidity, and the development of the industry in which it operates, may differ materially from the forward-looking statements contained in this press release. Any forward-looking statements that Cytokinetics makes in this press release speak only as of the date of this press release. Cytokinetics assumes no obligation to update its forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.
CYTOKINETICS® and the CYTOKINETICS and C-shaped logo are registered trademarks of Cytokinetics in the U.S. and certain other countries.
Contact:
Cytokinetics
Diane Weiser
Senior Vice President, Corporate Communications, Investor Relations
(415) 290-7757
| Cytokinetics, Incorporated | ||||||||
| Condensed Consolidated Balance Sheets | ||||||||
| (in thousands) | ||||||||
| September 30, 2023 | December 31, 2022 | |||||||
| (unaudited) | ||||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and short term investments | $ | 539,239 | $ | 782,577 | ||||
| Other current assets | 22,177 | 12,609 | ||||||
| Total current assets | 561,416 | 795,186 | ||||||
| Long-term investments | 15,468 | 46,708 | ||||||
| Property and equipment, net | 75,614 | 80,453 | ||||||
| Operating lease right-of-use assets | 79,929 | 82,737 | ||||||
| Other assets | 8,187 | 9,691 | ||||||
| Total assets | $ | 740,614 | $ | 1,014,775 | ||||
| LIABILITIES AND STOCKHOLDERS’ DEFICIT | ||||||||
| Current liabilities: | ||||||||
| Accounts payable and accrued liabilities | $ | 46,750 | $ | 69,707 | ||||
| Short-term operating lease liabilities | 17,236 | 12,829 | ||||||
| Other current liabilities | 13,737 | 2,081 | ||||||
| Total current liabilities | 77,723 | 84,617 | ||||||
| Term loan, net | 60,885 | 63,810 | ||||||
| Convertible notes, net | 548,134 | 545,808 | ||||||
| Liabilities related to revenue participation right purchase agreements, net | 370,049 | 300,501 | ||||||
| Long-term operating lease liabilities | 122,216 | 126,895 | ||||||
| Other non-current liabilities | 408 | 1,044 | ||||||
| Total liabilities | 1,179,415 | 1,122,675 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders’ deficit: | ||||||||
| Common stock | 94 | 94 | ||||||
| Additional paid-in capital | 1,537,321 | 1,481,590 | ||||||
| Accumulated other comprehensive loss | (874 | ) | (3,590 | ) | ||||
| Accumulated deficit | (1,975,342 | ) | (1,585,994 | ) | ||||
| Total stockholders’ deficit | (438,801 | ) | (107,900 | ) | ||||
| Total liabilities and stockholders’ deficit | $ | 740,614 | $ | 1,014,775 | ||||
| Cytokinetics, Incorporated | |||||||||||||||||||
| Condensed Consolidated Statements of Operations | |||||||||||||||||||
| (in thousands except per share data) | |||||||||||||||||||
| (unaudited) | |||||||||||||||||||
| Three Months Ended | Nine Months Ended | ||||||||||||||||||
| September 30, 2023 | September 30, 2022 | September 30, 2023 | September 30, 2022 | ||||||||||||||||
| Revenues: | |||||||||||||||||||
| Research and development revenues | $ | 378 | $ | 2,515 | $ | 3,358 | $ | 4,631 | |||||||||||
| Milestone revenues | — | — | 2,500 | 1,000 | |||||||||||||||
| Realization of revenue participation right purchase agreement | — | — | — | 87,000 | |||||||||||||||
| Total revenues | 378 | 2,515 | 5,858 | 92,631 | |||||||||||||||
| Operating expenses: | |||||||||||||||||||
| Research and development | 82,532 | 62,734 | 245,147 | 165,795 | |||||||||||||||
| General and administrative | 40,111 | 48,222 | 129,498 | 124,008 | |||||||||||||||
| Total operating expenses | 122,643 | 110,956 | 374,645 | 289,803 | |||||||||||||||
| Operating loss | (122,265 | ) | (108,441 | ) | (368,787 | ) | (197,172 | ) | |||||||||||
| Interest expense | (7,136 | ) | (6,804 | ) | (21,142 | ) | (12,357 | ) | |||||||||||
| Loss on extinguishment of debt | — | (22,246 | ) | — | (24,939 | ) | |||||||||||||
| Non-cash interest expense on liabilities related to revenue participation right purchase agreements | (6,860 | ) | (8,963 | ) | (19,462 | ) | (22,530 | ) | |||||||||||
| Interest and other income, net | 6,839 | 4,144 | 20,043 | 5,423 | |||||||||||||||
| Net loss | $ | (129,422 | ) | $ | (142,310 | ) | $ | (389,348 | ) | $ | (251,575 | ) | |||||||
| Net loss per share — basic and diluted | $ | (1.35 | ) | $ | (1.52 | ) | $ | (4.07 | ) | $ | (2.85 | ) | |||||||
| Weighted-average number of shares used in computing net loss per share — basic and diluted | 96,071 | 93,758 | 95,666 | 88,195 | |||||||||||||||
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