SOUTH SAN FRANCISCO, Calif., Nov. 06, 2024 (GLOBE NEWSWIRE) -- Cytokinetics, Incorporated (Nasdaq: CYTK) reported a management update and financial results for the third quarter of 2024.
“The progress we made in the third quarter reflects disciplined planning and prudent capital deployment throughout 2024 that has laid the foundation for our specialty cardiology business. The submission of the NDA for aficamten is an important regulatory milestone that brings us one step closer to the potential approval and commercial launch of aficamten in the United States alongside the scale-up of global workstreams,” said Robert I. Blum, Cytokinetics’ President and Chief Executive Officer. “While aficamten remains our top priority, our development pipeline is advancing and expanding with later-stage cardiovascular drug candidates as well as an earlier potential medicine focused to neuromuscular indications. With more than $1 billion on the balance sheet and access to additional long-term capital, we are well-funded and well-prepared to sustain momentum into 2025 with objective to deliver on the promise of our science for patients and to deliver meaningfully increased value to shareholders.”
Q3 and Recent Highlights
Cardiac Muscle Programs
aficamten (cardiac myosin inhibitor)
omecamtiv mecarbil (cardiac myosin activator)
CK-4021586 (CK-586, cardiac myosin inhibitor)
Pre-Clinical Development and Ongoing Research
Corporate
Third Quarter 2024 Financial Results
Cash, Cash Equivalents and Investments
Revenues
Research and Development (R&D) Expenses
General and Administrative (G&A) Expenses
Net Income (Loss)
2024 Financial Guidance
The company is reiterating its full year 2024 financial guidance:
2024 Guidance | |
GAAP Operating Expense[1] | $555m to $575m |
Non-cash Expense[2] Included in GAAP Operating Expense | $110m to $105m |
Non-GAAP Operating Expense[3] | $445m to $470m |
Net Cash Utilization[4] | $400m to $420m |
The financial guidance does not include the effect of GAAP adjustments as may be caused by events that occur subsequent to publication of this guidance including but not limited to Business Development activities.
[1]GAAP operating expense comprised of R&D and G&A expenses.
[2]Non-cash operating expense comprised of stock-based compensation and depreciation.
[3]Non-GAAP operating expense comprised of R&D and G&A expenses but excludes non-cash operating expense.
[4]Net cash utilization is a non-GAAP financial measure that we define as our ending 2023 cash, cash equivalents, and investments balance of $655 million plus the net proceeds of $707 million received from the sale of common stock (through the at-the-market facility, public offerings, and stock purchase agreement with Royalty Pharma) plus proceeds of $200 million received from the structured financing agreement with Royalty Pharma announced on May 22, 2024 minus our projected ending 2024 cash, cash equivalents, and investments balance of between $1,142 million and $1,162 million.
Conference Call and Webcast Information
Members of Cytokinetics’ senior management team will review the company’s third quarter 2024 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 2024 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 muscle biology-directed drug candidates 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. Following positive results from SEQUOIA-HCM, the pivotal Phase 3 clinical trial evaluating aficamten, a next-in-class cardiac myosin inhibitor, in obstructive hypertrophic cardiomyopathy (HCM), Cytokinetics submitted an NDA for aficamten to the U.S. Food & Drug Administration and is progressing regulatory submissions for aficamten for the treatment of obstructive HCM in Europe. Aficamten is also currently being evaluated in MAPLE-HCM, a Phase 3 clinical trial of aficamten as monotherapy compared to metoprolol as monotherapy in patients with obstructive HCM, ACACIA-HCM, a Phase 3 clinical trial of aficamten in patients with non-obstructive HCM, CEDAR-HCM, a clinical trial of aficamten in a pediatric population with obstructive HCM, and FOREST-HCM, an open-label extension clinical study of aficamten in patients with HCM. Cytokinetics is also developing omecamtiv mecarbil, a cardiac muscle activator, in patients with heart failure with severely reduced ejection fraction (HFrEF), CK-586, a cardiac myosin inhibitor with a mechanism of action distinct from aficamten for the potential treatment of heart failure with preserved ejection fraction (HFpEF), and CK-089, a fast skeletal muscle troponin activator (FSTA) for the potential treatment of a specific type of muscular dystrophy.
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 submit a marketing authorisation application for aficamten in the European Union in the fourth quarter of 2024, our ability to complete enrollment of ACACIA-HCM in 2025, our ability to start COMET-HF or AMBER-HFpEF in the fourth quarter of 2024, and to commence a Phase 1 study of CK-089 in the fourth quarter of 2024, 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 relating to the potential patient population who could benefit from aficamten, omecamtiv mecarbil, CK-586, CK-089 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 Corxel (f/k/a Ji Xing); statements relating to our operating expenses or cash utilization for the remainder of 2024, and statements relating to our cash balance at year-end 2024 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 2023. 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 Affairs
(415) 290-7757
Cytokinetics, Incorporated | |||||||
Condensed Consolidated Balance Sheets | |||||||
(in thousands) | |||||||
September 30, 2024 | December 31, 2023 | ||||||
(unaudited) | |||||||
ASSETS | |||||||
Current assets: | |||||||
Cash and short term investments | $ | 1,011,692 | $ | 614,824 | |||
Other current assets | 6,909 | 13,227 | |||||
Total current assets | 1,018,601 | 628,051 | |||||
Long-term investments | 269,168 | 40,534 | |||||
Property and equipment, net | 64,222 | 68,748 | |||||
Operating lease right-of-use assets | 76,344 | 78,987 | |||||
Other assets | 7,725 | 7,996 | |||||
Total assets | $ | 1,436,060 | $ | 824,316 | |||
LIABILITIES AND STOCKHOLDERS’ DEFICIT | |||||||
Current liabilities: | |||||||
Accounts payable and accrued liabilities | $ | 61,407 | $ | 64,148 | |||
Short-term operating lease liabilities | 18,856 | 17,891 | |||||
Current portion of long-term debt | 11,520 | 10,080 | |||||
Derivative liabilities measured at fair value | 12,500 | — | |||||
Other current liabilities | 5,529 | 10,559 | |||||
Total current liabilities | 109,812 | 102,678 | |||||
Term loan, net | 93,017 | 58,384 | |||||
Convertible notes, net | 551,481 | 548,989 | |||||
Liabilities related to revenue participation right purchase agreements, net | 448,509 | 379,975 | |||||
Long-term operating lease liabilities | 114,752 | 120,427 | |||||
Liabilities related to RPI Transactions measured at fair value | 132,400 | — | |||||
Other non-current liabilities | — | 186 | |||||
Total liabilities | 1,449,971 | 1,210,639 | |||||
Commitments and contingencies | |||||||
Stockholders' deficit | |||||||
Common stock | 118 | 102 | |||||
Additional paid-in capital | 2,532,328 | 1,725,823 | |||||
Accumulated other comprehensive income (loss) | 5,387 | (10 | ) | ||||
Accumulated deficit | (2,551,744 | ) | (2,112,238 | ) | |||
Total stockholders' deficit | (13,911 | ) | (386,323 | ) | |||
Total liabilities and stockholders' deficit | $ | 1,436,060 | $ | 824,316 | |||
Cytokinetics, Incorporated | |||||||||||||||
Condensed Consolidated Statements of Operations | |||||||||||||||
(in thousands except per share data) | |||||||||||||||
(unaudited) | |||||||||||||||
Three Months Ended | Nine Months Ended | ||||||||||||||
September 30, 2024 | September 30, 2023 | September 30, 2024 | September 30, 2023 | ||||||||||||
Revenues: | |||||||||||||||
Research and development revenues | $ | 463 | $ | 378 | $ | 1,547 | $ | 3,358 | |||||||
Milestone revenues | — | — | — | 2,500 | |||||||||||
Total revenues | 463 | 378 | 1,547 | 5,858 | |||||||||||
Operating expenses: | |||||||||||||||
Research and development | 84,612 | 82,532 | 245,779 | 245,147 | |||||||||||
General and administrative | 56,652 | 40,111 | 152,976 | 129,498 | |||||||||||
Total operating expenses | 141,264 | 122,643 | 398,755 | 374,645 | |||||||||||
Operating loss | (140,801 | ) | (122,265 | ) | (397,208 | ) | (368,787 | ) | |||||||
Interest expense | (8,928 | ) | (7,136 | ) | (28,763 | ) | (21,142 | ) | |||||||
Non-cash interest expense on liabilities related to revenue participation right purchase agreements | (13,370 | ) | (6,860 | ) | (35,155 | ) | (19,462 | ) | |||||||
Interest and other income, net | 17,054 | 6,839 | 36,520 | 20,043 | |||||||||||
Change in fair value of derivative liabilities | 700 | — | 100 | — | |||||||||||
Change in fair value of liabilities related to RPI Transactions | (15,200 | ) | — | (15,000 | ) | — | |||||||||
Net loss | $ | (160,545 | ) | $ | (129,422 | ) | $ | (439,506 | ) | $ | (389,348 | ) | |||
Net loss per share — basic and diluted | $ | (1.36 | ) | $ | (1.35 | ) | $ | (4.00 | ) | $ | (4.07 | ) | |||
Weighted-average number of shares used in computing net loss per share — basic and diluted | 117,685 | 96,071 | 109,932 | 95,666 | |||||||||||
Last Trade: | US$49.86 |
Daily Change: | -1.23 -2.41 |
Daily Volume: | 1,028,600 |
Market Cap: | US$5.870B |
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