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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of report (Date of earliest event reported): March 20, 2025
ARMATA PHARMACEUTICALS, INC.
(Exact name of Registrant as specified in its charter)
Washington |
001-37544 |
91-1549568 |
(State or other jurisdiction of |
(Commission File Number) |
(IRS Employer Identification No.) |
|
5005 McConnell Avenue Los Angeles, California |
90066 |
(Address of principal executive offices) |
(Zip Code) |
(310) 655-2928
(Registrant’s Telephone number)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the Registrant under any of the following provisions (see General Instruction A.2. below):
☐Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
☐Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
☐Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Securities registered pursuant to Section 12(b) of the Act:
Title of Each Class |
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Trading Symbol(s) |
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Name of Each Exchange on Which Registered |
Common Stock |
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ARMP |
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NYSE American |
Item 2.02Results of Operations and Financial Condition.
On March 20, 2025, Armata Pharmaceuticals, Inc. (the “Company”) announced its financial results for the three months and full fiscal year ended December 31, 2024, in the press release furnished hereto as Exhibit 99.1.
The information in this Item 2.02 and the attached Exhibit 99.1 is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities and Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that Section. The information in this Item 2.02 and the attached Exhibit 99.1 shall not be incorporated by reference into any registration statement or other document pursuant to the Securities Act of 1933, as amended.
Item 9.01Financial Statements and Exhibits.
(d)Exhibits.
Exhibit |
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Description |
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104 |
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Cover Page Interactive Data File (embedded within Inline XBRL document). |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
Date: March 20, 2025 |
Armata Pharmaceuticals, Inc. |
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By: |
/s/ David House |
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Name: |
David House |
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Title: |
Senior Vice President, Finance and Principal Financial Officer |
Exhibit 99.1
Armata Pharmaceuticals Announces Fourth Quarter and Full-Year 2024 Results and
Provides Corporate Update
LOS ANGELES, CA, March 20, 2025 - Armata Pharmaceuticals, Inc. (NYSE American: ARMP) (“Armata” or the “Company”), a clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced financial results for its fourth quarter and full-year ended December 31, 2024, and provided a corporate update.
Fourth Quarter 2024 and Recent Developments:
| ● | Announced encouraging topline results from its Phase 2 Tailwind study evaluating inhaled AP-PA02 as a potential treatment for chronic pulmonary disease; Pseudomonas aeruginosa (“P. aeruginosa” or “P.a.”) infection in non-cystic fibrosis bronchiectasis (“NCFB”) patients. |
| o | The Phase 2 Tailwind study represents the second successful clinical trial for AP-PA02, Armata's lead pulmonary candidate, which was first evaluated in people with cystic fibrosis in the Phase 1b/2a SWARM-P.a. trial that completed in 2023; |
| o | Inhaled AP-PA02 was well-tolerated, with treatment-emergent adverse events mild and self-limiting; |
| o | Post-hoc intent-to-treat analysis demonstrated a statistically significant reduction of P.a. colony forming units (“CFUs”) at one and two weeks post-dosing. Approximately one-third of all subjects treated with phage monotherapy exhibited at least a 2-log CFU reduction in P.a.; and |
| o | Data suggest AP-PA02 alone is as effective as AP-PA02 plus antibiotics in reducing P.a. CFUs in the lungs of NCFB patients, and indicates the potential for phage therapy to reduce reliance on chronic antibiotic use. |
| ● | Completed enrollment of Phase 1b/2a diSArm study of intravenous (“IV”) AP-SA02 as a potential treatment for Staphylococcus aureus (“S. aureus”) bacteremia. |
| o | Blinded data demonstrates AP-SA02 is well-tolerated following IV administration of up to 5E10 plaque forming units (“PFUs”) every six hours (2E11 PFU every 24 hours) for five days; |
| o | Persistence of AP-SA02 in a subset of complicated bacteremia subjects is consistent with in vivo phage amplification despite 48-72 hours of broad-spectrum IV antibiotics -- unblinding is critical to understand subjects’ clinical presentation; |
| o | Topline data anticipated in the first half of 2025; and |
| o | Anticipate that findings from the diSArm study will inform the design of a pivotal trial strategy to be discussed with the U.S. Food and Drug Administration (the “FDA”) that may enable Armata to obtain agreement on a path to potential approval. |
| ● | Further advanced bacteriophage science through presentations and publications. |
| o | Presented at 7th Annual Phage Therapy Summit, March 11-13, 2025, Boston, MA; |
| o | Presented at 5th Annual Phage Futures Meeting, November 19, 2024, Boston, MA; and |
| o | Announced structural biology publication in the journal Communications Biology describing a representative phage in Armata's clinical candidate, AP-PA02. |
| ● | In March 2025, entered into a $10.0 million secured credit agreement with Innoviva Strategic Opportunities LLC, a wholly-owned subsidiary of Innoviva, Armata's principal shareholder. |
“During the fourth quarter, we achieved another significant clinical milestone with encouraging topline results from our Phase 2 Tailwind study evaluating inhaled AP-PA02 in NCFB patients as both monotherapy and in combination with inhaled anti-pseudomonal antibiotics,” stated Dr. Deborah Birx, Chief Executive Officer of Armata. “This was the second successful clinical evaluation of AP-PA02 following our Phase 1b/2a SWARM-P.a. trial in cystic fibrosis patients. We believe the learnings gained from the two completed Phase 2 studies position Armata to design a pivotal trial to evaluate AP-PA02 as an alternative to antibiotics in NCFB patients with chronic pulmonary P. aeruginosa infection.”
“We also completed enrollment of our Phase 1b/2a diSArm study evaluating our high purity phage product candidate, AP-SA02, as a potential treatment for S. aureus bacteremia. We expect to report topline results in the first half of this year, and believe data will provide valuable insights into the safety and tolerability of AP-SA02 at high intravenous doses, and inform the dose and schedule to be studied in a larger efficacy study, which we plan to discuss with the FDA this year.”
“We remain committed to developing a definitive efficacy trial focused on phage as an alternative to broad-spectrum antibiotics and/or antibiotic-sparing to decrease the utilization of traditional antibiotics and their detrimental impact on the normal human microbiome. I believe we are well positioned to achieve value-creating milestones in 2025 as the Armata team continues to work to introduce a novel therapeutic class to help fight the global health crisis of antimicrobial resistance,” Dr. Birx concluded.
Fourth Quarter 2024 Financial Results
Grant Revenue. The Company recognized grant revenue of $1.2 million for the three months ended December 31, 2024 as compared to $1.5 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 December 31, 2024 were approximately $8.5 million as compared to approximately $7.9 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 December 31, 2024 were approximately $3.3 million as compared to approximately $3.2 million for the comparable period in 2023. The increase was mainly related to an increase of $0.3 million in personnel related expenses during the fourth quarter of 2024, offset in part by a decrease of $0.2 million in professional services.
Loss from Operations. Loss from operations for the three months ended December 31, 2024 was approximately $10.5 million as compared to a loss from operations of approximately $9.6 million for the comparable period in 2023.
Net Income (Loss). The net income for the fourth quarter of 2024 was $2.6 million, or $0.07 per share on a basic and $(0.23) per share on a diluted basis, as compared to a net loss of $19.8 million, or $(0.55) per share on both a basic and diluted basis, for the comparable period in 2023. The net income for the quarter ended December 31, 2024 included non-cash gain from the changes in fair value of convertible loan of $14.2 million and non-cash gain from debt extinguishment of $2.2 million, as compared to $8.9 million loss from the changes in fair value of convertible loan for the quarter ended December 31, 2023.
Cash and Equivalents. As of December 31, 2024, Armata held approximately $14.8 million of cash and cash equivalents and restricted cash, as compared to $19.2 million as of December 31, 2023.
On March 12, 2025, the Company entered into a credit and security agreement for a loan in an aggregate amount of $10.0 million with Innoviva SO. The loan bears interest at an annual rate of 14% and matures on March 12, 2026. Principal and accrued interest are payable at maturity. The Company and Innoviva also entered into amendments to the three pre-existing credit and security agreements in order to, among other things, extend the maturity dates under such agreements to March 12, 2026.
As of February 28, 2025, 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 high-purity 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 to support full commercialization.
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 20, 2025, 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)
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December 31, 2024 |
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December 31, 2023 |
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Assets |
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Current assets |
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Cash and cash equivalents |
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$ |
9,291 |
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$ |
13,523 |
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Prepaid expenses and other current assets |
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1,273 |
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2,265 |
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Other receivables |
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744 |
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3,363 |
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Total current assets |
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11,308 |
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19,151 |
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Property and equipment, net |
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13,241 |
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12,559 |
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Operating lease right-of-use asset |
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41,687 |
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44,717 |
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Intangible assets, net |
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13,746 |
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13,746 |
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Other long term assets |
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6,455 |
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8,190 |
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Total assets |
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$ |
86,437 |
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$ |
98,363 |
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Liabilities and stockholders’ deficit |
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Accounts payable, accrued and other current liabilities |
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9,295 |
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16,461 |
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Term debt, current |
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38,954 |
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— |
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Total current liabilities |
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$ |
48,249 |
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$ |
16,461 |
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Convertible loan, non-current |
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32,897 |
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58,633 |
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Term debt, non-current |
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22,539 |
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23,674 |
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Operating lease liabilities, net of current portion |
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27,694 |
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28,583 |
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Deferred tax liability |
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3,077 |
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3,077 |
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Total liabilities |
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134,456 |
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130,428 |
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Stockholders’ deficit |
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(48,019) |
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(32,065) |
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Total liabilities and stockholders’ deficit |
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$ |
86,437 |
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$ |
98,363 |
|
Armata Pharmaceuticals, Inc.
Condensed Consolidated Statements of Operations
(in thousands, except share and per share data)
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Three Months Ended |
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Year Ended |
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December 31, |
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December 31, |
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2024 |
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2023 |
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2024 |
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2023 |
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Grant revenue |
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$ |
1,235 |
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$ |
1,528 |
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$ |
5,174 |
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$ |
4,529 |
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Operating expenses |
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Research and development |
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8,450 |
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7,928 |
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34,426 |
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33,770 |
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General and administrative |
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3,323 |
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3,179 |
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13,184 |
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11,649 |
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Total operating expenses |
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11,773 |
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11,107 |
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47,610 |
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45,419 |
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Operating loss |
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(10,538) |
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(9,579) |
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(42,436) |
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(40,890) |
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Interest income |
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130 |
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68 |
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697 |
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179 |
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Interest expense |
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(3,281) |
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(1,450) |
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(10,742) |
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(2,626) |
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Change in fair value of convertible loan |
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14,123 |
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(8,886) |
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31,399 |
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(21,845) |
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Gain (loss) on debt and convertible loan extinguishments |
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2,166 |
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— |
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2,166 |
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(3,863) |
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Net income (loss) |
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$ |
2,600 |
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$ |
(19,847) |
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$ |
(18,916) |
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$ |
(69,045) |
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Per share information: |
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Net income (loss) per share, basic |
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$ |
0.07 |
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$ |
(0.55) |
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$ |
(0.52) |
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$ |
(1.91) |
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Weighted average shares outstanding, basic |
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36,183,067 |
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36,100,869 |
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36,160,848 |
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36,075,555 |
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Net loss per share, diluted |
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$ |
(0.23) |
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$ |
(0.55) |
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$ |
(0.89) |
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$ |
(1.91) |
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Weighted average shares outstanding, diluted |
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59,082,190 |
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36,100,869 |
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59,059,971 |
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36,075,555 |
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Armata Pharmaceuticals, Inc.
Condensed Consolidated Statements of Cash Flows
(in thousands)
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Year Ended December 31, |
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2024 |
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2023 |
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Operating activities: |
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Net loss |
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$ |
(18,916) |
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$ |
(69,045) |
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Adjustments required to reconcile net loss to net cash used in operating activities: |
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Depreciation and amortization expense |
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1,325 |
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|
972 |
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Stock-based compensation expense |
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2,893 |
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|
938 |
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Change in fair value of convertible loan |
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(31,399) |
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21,845 |
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Non-cash interest expense |
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10,758 |
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2,573 |
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Non-cash interest income |
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— |
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(22) |
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Gain (loss) on debt and convertible loan extinguishments |
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(2,166) |
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3,863 |
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Change in right-of-use asset |
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2,053 |
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1,018 |
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Loss from disposal of property and equipment |
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— |
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81 |
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Changes in operating assets and liabilities: |
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(2,099) |
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(9,646) |
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Net cash used in operating activities |
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(37,551) |
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(47,423) |
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Investing activities: |
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Purchases of property and equipment |
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(1,879) |
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(8,144) |
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Proceeds from sale of property and equipment |
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— |
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10 |
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Net cash used in investing activities |
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(1,879) |
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(8,134) |
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Financing activities: |
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Proceeds from issuance of convertible loan, net of issuance costs |
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— |
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29,101 |
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Proceeds from issuance of term debt, net of issuance costs |
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34,889 |
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24,925 |
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Payments for taxes related to net share settlement of equity awards |
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(61) |
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(43) |
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Proceeds from exercise of stock options |
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130 |
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|
5 |
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Net cash provided by financing activities |
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34,958 |
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53,988 |
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Net decrease in cash, cash equivalents and restricted cash |
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(4,472) |
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|
(1,569) |
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Cash, cash equivalents and restricted cash, beginning of period |
|
|
19,243 |
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|
20,812 |
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Cash, cash equivalents and restricted cash, end of period |
|
$ |
14,771 |
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$ |
19,243 |
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Year Ended December 31, |
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2024 |
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2023 |
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Cash and cash equivalents |
|
$ |
9,291 |
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$ |
13,523 |
Restricted cash |
|
|
5,480 |
|
|
5,720 |
Cash, cash equivalents and restricted cash, end of period |
|
$ |
14,771 |
|
$ |
19,243 |