Armata Pharmaceuticals Announces Third Quarter 2024 Results and Provides Corporate Update
LOS ANGELES, Nov. 13, 2024 /PRNewswire/ -- Armata Pharmaceuticals, Inc. (NYSE American: ARMP) ("Armata" or the "Company"), a biotechnology company focused on high-purity, pathogen-specific bacteriophage therapeutics for antibiotic-resistant and difficult-to-treat bacterial infections, today announced financial results for its third quarter ended September 30, 2024, and provided a corporate update.
Third Quarter 2024 and Recent Developments:
-- Completed enrollment of the Phase 2 study ("Tailwind") of inhaled AP-PA02 in patients with non-cystic fibrosis bronchiectasis ("NCFB") and chronic pulmonary Pseudomonas aeruginosa ("P. aeruginosa") infection. -- Topline data expected by year-end. -- Working towards initiating a pivotal bronchiectasis trial in 2025 for chronic pulmonary P. aeruginosa infection. -- Completed enrollment of Phase 1b/2a study ("diSArm") of intravenous AP-SA02 in patients with Staphylococcus aureus ("S. aureus") bacteremia. -- Topline data expected in the first quarter of 2025. -- Moving towards initiating a pivotal S. aureus bacteremia trial in 2025. -- Received $5.25 million of additional non-dilutive funding to support the diSArm study pursuant to a previously announced Department of Defense grant, received through the Medical Technology Enterprise Consortium ("MTEC") and managed by the Naval Medical Research Command (NMRC) - Naval Advanced Medical Development (NAMD) with funding from the Defense Health Agency and Joint Warfighter Medical Research Program. -- Further advanced bacteriophage science through presentations and publications: -- Announced publication in Communications Biology describing the structure of a Pseudomonas phage, representative of a family present in the clincial candidate cocktail AP-PA02. -- Delivered a poster presentation at the 2024 Military Health System Research Symposium (MHSRS), held August 26-29, in Kissimmee, Florida. -- Delivered an oral presentation on advancing bacteriophage therapy at Viruses of Microbes 2024, held July 15-19, in Cairns, Australia. -- Appointed life sciences accounting and finance veteran David House as Senior Vice President, Finance. -- Amended convertible debt and 2023 credit agreement to extend the maturity dates from January 10, 2025 to January 10, 2026.
"During the third quarter, we completed enrollment of our Phase 2 Tailwind study of inhaled AP-PA02 in NCFB patients with chronic P. aeruginosa infection, and remain on-track to report topline data from this study by the end of this year," stated Dr. Deborah Birx, Chief Executive Officer of Armata. "This will mark our second Phase 2 data readout for inhaled AP-PA02, following prior successful evaluation in patients with cystic fibrosis in the Phase 1b/2a SWARM-P.a. clinical trial last year. We plan to meet with the U.S. FDA to align on the design of a pivotal Phase 3 bronchiectasis study for inhaled AP-PA02 as a pulmonary disease therapeutic which we are working towards initiating in 2025."
"Additionally, we have completed enrollment of our Phase 1b/2a diSArm study evaluating intravenous AP-SA02 as a potential treatment for S. aureus bacteremia. The high purity of Armata's intravenously-administered phage drug products enabled dose escalation to 2E11 PFU every 24 hours for five days, which was well-tolerated. We look forward to topline data in the first quarter of 2025 that should inform the optimal dose of AP-SA02 to be evaluated in a larger definitive efficacy study that we are planning to initiate in 2025."
"With two Phase 2 data readouts expected near-term, we believe we continue to add to the body of evidence demonstrating the potential of phage therapy, either as an alternative to or in combination with current standard of care antibiotics, to combat antibiotic-resistant and difficult-to-treat bacterial infections. I am delighted with our progress to date, and look forward to potential major value inflection points in 2025 and beyond," Dr. Birx concluded.
Third Quarter 2024 Financial Results
Grant Revenue. The Company recognized grant revenue of $3.0 million for the three months ended September 30, 2024 as compared to $1.2 million in the comparable period in 2023, which represents MTEC's share of the costs incurred for the Company's AP-SA02 program for the treatment of S. aureus bacteremia.
Research and Development. Research and development expenses for the three months ended September 30, 2024 were approximately $9.5 million as compared to approximately $8.0 million for the comparable period in 2023. The Company continues to invest in clinical related expenses associated with its primary development programs.
General and Administrative. General and administrative expenses for the three months ended September 30, 2024 were approximately $3.2 million as compared to approximately $3.6 million for the comparable period in 2023. The decrease was mainly related to a decrease of $1.0 million in professional services during the third quarter of 2024, offset in part by an increase of $0.6 million in personnel related expenses.
Loss from Operations. Loss from operations for the three months ended September 30, 2024 was approximately $9.8 million as compared to a loss from operations of approximately $10.3 million for the comparable period in 2023.
Net Loss. The net loss for the third quarter of 2024 was $5.5 million, or $0.15 per share on both a basic and diluted basis, as compared to a net loss of $31.2 million, or $0.86 per share on both a basic and diluted basis, for the comparable period in 2023. The net loss for the quarter ended September 30, 2024 included non-cash gain from changes in fair value of convertible debt of $6.9 million, as compared to $15.8 million loss from changes in fair value of convertible debt for the quarter ended September 30, 2023.
Cash and Equivalents. As of September 30, 2024, Armata held approximately $17.1 million of unrestricted cash and cash equivalents, as compared to $13.5 million as of December 31, 2023.
As of November 13, 2024, there were approximately 36.2 million common shares outstanding.
About Armata Pharmaceuticals, Inc.
Armata is a clinical-stage biotechnology company focused on the development of pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections using its proprietary bacteriophage-based technology. Armata is developing and advancing a broad pipeline of natural and synthetic phage candidates, including clinical candidates for Pseudomonas aeruginosa, Staphylococcus aureus, and other pathogens. Armata is committed to advancing phage therapy with drug development expertise that spans bench to clinic including in-house phage specific cGMP manufacturing.
Forward Looking Statements
This communication contains "forward-looking" statements as defined by the Private Securities Litigation Reform Act of 1995. These statements relate to future events, results or to Armata's future financial performance and involve known and unknown risks, uncertainties and other factors which may cause Armata's actual results, performance or events to be materially different from any future results, performance or events expressed or implied by the forward-looking statements. In some cases, you can identify these statements by terms such as "anticipate," "believe," "could," "estimate," "expect," "intend," "may," "plan," "potential," "predict," "project," "should," "will," "would" or the negative of those terms, and similar expressions. These forward-looking statements reflect management's beliefs and views with respect to future events and are based on estimates and assumptions as of the date of this communication and are subject to risks and uncertainties including risks related to Armata's development of bacteriophage-based therapies; ability to staff and maintain its production facilities under fully compliant current Good Manufacturing Practices; ability to meet anticipated milestones in the development and testing of the relevant product; ability to be a leader in the development of phage-based therapeutics; ability to achieve its vision, including improvements through engineering and success of clinical trials; ability to successfully complete preclinical and clinical development of, and obtain regulatory approval of its product candidates and commercialize any approved products on its expected timeframes or at all; and Armata's estimates regarding anticipated operating losses, capital requirements and needs for additional funds. Additional risks and uncertainties relating to Armata and its business can be found under the caption "Risk Factors" and elsewhere in Armata's filings and reports with the SEC, including in Armata's Annual Report on Form 10-K, filed with the SEC on March 21, 2024, and in its subsequent filings with the SEC.
Armata expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Armata's expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based.
Media Contacts:
At Armata:
Pierre Kyme
ir@armatapharma.com
310-665-2928
Investor Relations:
Joyce Allaire
LifeSci Advisors, LLC
jallaire@lifesciadvisors.com
212-915-2569
Armata Pharmaceuticals, Inc. Condensed Consolidated Balance Sheets (in thousands) (unaudited) September 30, 2024 December 31, 2023 Assets Current assets Cash and cash equivalents $ 17,141 $ 13,523 Prepaid expenses and other current assets 3,029 2,265 Other receivables 2,219 3,363 Total current assets 22,389 19,151 Property and equipment, net 13,616 12,559 Operating lease right-of-use asset 42,251 44,717 Intangible assets, net 13,746 13,746 Other long term assets 6,235 8,190 Total assets $ 98,237 $ 98,363 Liabilities and stockholders' deficit Accounts payable, accrued and other current liabilities 10,801 16,461 Convertible debt, current 41,357 Term debt, current 66,046 Total current liabilities $ 118,204 $ 16,461 Convertible debt, non-current 58,633 Term debt, non-current 23,674 Operating lease liabilities, net of current portion 27,929 28,583 Deferred tax liability 3,077 3,077 Total liabilities 149,210 130,428 Stockholders' deficit (50,973) (32,065) Total liabilities and stockholders' deficit $ 98,237 $ 98,363
Armata Pharmaceuticals, Inc. Condensed Consolidated Statements of Operations (in thousands, except share and per share data ) (unaudited) Three Months Ended Nine Months Ended September 30, September 30, 2024 2023 2024 2023 Grant revenue $ 2,973 $ 1,225 $ 3,939 $ 3,001 Operating expenses: Research and development 9,485 7,978 25,975 25,842 General and administrative 3,244 3,583 9,861 8,470 Total operating expenses 12,729 11,561 35,836 34,312 Operating loss (9,756) (10,336) (31,897) (31,311) Interest income 294 47 567 111 Interest expense (2,923) (1,176) (7,462) (1,176) Change in fair value of convertible debt 6,904 (15,833) 17,276 (12,959) Loss on convertible debt extinguishment (3,863) (3,863) Net loss $ (5,481) $ (31,161) $ (21,516) $ (49,198) Per share information: Net loss per share, basic and diluted $ (0.15) $ (0.86) $ (0.60) $ (1.36) Weighted average shares outstanding, basic and diluted 36,180,124 36,086,990 36,153,388 36,067,025
Armata Pharmaceuticals, Inc. Condensed Consolidated Statements of Cash Flows (in thousands) (unaudited) Nine Months Ended September 30, 2024 2023 Operating activities: Net loss $ (21,516) $ (49,198) Adjustments required to reconcile net loss to net cash used in operating activities: Depreciation and amortization expense 945 679 Stock-based compensation expense 2,539 745 Change in fair value of convertible debt (17,276) 12,959 Non-cash interest expense 7,483 1,176 Loss on convertible debt extinguishment 3,863 Change in right-of-use asset 1,489 662 Changes in operating assets and liabilities: (3,288) (10,203) Net cash used in operating activities (29,624) (39,317) Investing activities: Purchases of property and equipment (1,956) (5,744) Net cash used in investing activities (1,956) (5,744) Financing activities: Proceeds from issuance of convertible debt, net of issuance costs 29,101 Proceeds from issuance of term debt, net of issuance costs 34,889 24,925 Payments for taxes related to net share settlement of equity awards (61) Proceeds from exercise of stock options 130 5 Net cash provided by financing activities 34,958 54,031 Net increase in cash, cash equivalents and restricted cash 3,378 8,970 Cash, cash equivalents and restricted cash, beginning of period 19,243 20,812 Cash, cash equivalents and restricted cash, end of period $ 22,621 $ 29,782 Nine Months Ended September 30, 2024 2023 Cash and cash equivalents $ 17,141 $ 23,958 Restricted cash 5,480 5,824 Cash, cash equivalents and restricted cash, end of period $ 22,621 $ 29,782
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