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Armata Pharmaceuticals Announces Third Quarter 2023 Results and Provides Corporate Update

Key Takeaway: Armata Pharmaceuticals reported positive developments in its third quarter 2023, emphasizing progress in its bacteriophage therapeutics pipeline with accelerated enrollment in key clinical studies. The company's financial results showed a revenue increase, supported by grant funding from the U.S. Department of Defense and a rise in cash reserves. However, operational losses increased compared to the previous year, with rising general and administrative costs. They are nearing the completion of a new manufacturing facility aimed at bolstering their capacity for late-stage trials and partnership opportunities.

Market Sentiment Analysis

POSITIVE FACTORS

  • Accelerating enrollment in critical Phase 2a studies, indicating progress in clinical development.
  • Expected completion of Phase 2 studies in 2024, which will aid in advancing to Phase 3 trials.
  • Development of a new biologics manufacturing facility that enhances operational capacity and strategic positioning.

CONCERNS & RISKS

  • Increase in general and administrative expenses, raising concerns about operational efficiency.
  • Operational loss rose to $(10.3) million, higher than the previous year, highlighting continuing financial losses.

Full Press Release Details

Armata Pharmaceuticals Announces Third Quarter 2023 Results and
Provides Corporate Update
LOS ANGELES, Calif., November 14, 2023 -- Armata Pharmaceuticals, Inc. (NYSE American: ARMP) ("Armata" or the "Company"), a biotechnology company focused on pathogen-specific bacteriophage therapeutics for antibiotic-resistant and difficult-to-treat bacterial infections, today announced financial results for its third quarter ended September 30, 2023, and provided a corporate update.
Third Quarter 2023 and Recent Developments:
"During the third quarter, we continued to make meaningful progress advancing our pipeline of phage therapeutics that we believe can address the growing global health crisis of multidrug resistant bacterial infections," stated Dr. Deborah Birx, Chief Executive Officer. "Notably, we are seeing accelerating enrollment in the Phase 2a portion of our diSArm study of AP-SA02. Due to the continued high level of patient tolerance on the intravenous phage, we expect to escalate our dose throughout the Phase 2 trial to define the Phase 3 dose. We are developing AP-SA02 with financial support from the Department of Defense as a potential treatment for S. aureus bacteremia. We believe the current enrollment trends will result in completion of the Phase 2 study in 2024, which would allow us to design the pivotal Phase 3 trial."
"Regarding AP-PA02, we are also seeing accelerating enrollment in our ongoing Tailwind Phase 2 study of PA02 in non-cystic fibrosis bronchiectasis. Importantly, both our diSArm and Tailwind studies continue to demonstrate favorable safety and tolerability profiles, including IV administration twice per day over multiple days."
"We are also fast approaching the completion of the build-out of our advanced biologics manufacturing facility that will provide us with the capacity to execute our own late-stage trials while pursuing important partnering opportunities. When completed, this facility will represent a significant step towards firmly establishing our position as a leader in the development of phage-based therapeutics."
"I am pleased with our continued progress, our ability to contain costs despite one-time G&A expenses realized in the third quarter. I believe we are well positioned to sustain our current momentum while continuing to contain costs through the remainder of the year and into 2024," Dr. Birx concluded.
Third Quarter 2023 Financial Results
Grant Revenue. The Company recognized grant revenue of approximately $1.2 million for the three months ended September 30, 2023, which represents Medical Technology Enterprise Consortium ("MTEC")'s share of the costs incurred for the Company's AP-SA02 program for the treatment of Staphylococcus aureus bacteremia. The Company expects to receive $16.3 million in grant funding from MTEC administered by the U.S. Department of Defense and the Defense Health Agency and Joint Warfighter Medical Research Program. The Company recognized approximately $1.3 million of revenue in the comparable period in 2022.
Research and Development. Research and development expenses for the three months ended September 30, 2023 were approximately $8.0 million as compared to approximately $8.4 million for the comparable period in 2022. The decrease was primarily related to reduced personnel and related expenses, including recruiting expenses and stock-based compensation expense.
General and Administrative. General and administrative expenses for the three months ended September 30, 2023 were approximately $3.6 million as compared to approximately $1.6 million for the comparable period in 2022. The increase was primarily related to the increased legal and other professional services expenses, a one-time expense related to financing costs recognized as an expense during the three months ended September 30, 2023.
Loss from Operations. Loss from operations for the three months ended September 30, 2023 was $(10.3) million as compared to a loss from operations of approximately $(8.6) million for the comparable period in 2022.
Cash and Equivalents. As of September 30, 2023, Armata held approximately $24.0 million of unrestricted cash and cash equivalents, as compared to $14.9 million as of December 31, 2022. On July 11, 2023, Armata announced a new credit agreement with Innoviva for gross proceeds totaling $25.0 million.
As of November 14, 2023, there were approximately 36.1 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 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, including, without limitation, statements related to Armata's bacteriophage development programs, Armata's ability to set up or operate R&D and manufacturing facilities, Armata's ability to meet expected milestones, Armata's future success or failure, Armata's ability to be a leader in the development of phage-based therapeutics, and statements related to the timing and results of clinical trials, including the anticipated results of clinical trials of AP-PA02 and AP-SA02, Armata's ability to develop new products based on natural bacteriophages and synthetic bacteriophages and Armata's ability to obtain additional funding and capacity to repay, refinance, or restructure its existing debt and obligations. Any statements contained in this communication that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements are based upon Armata's current expectations. Forward-looking statements involve risks and uncertainties. Armata's actual results and the timing of events could differ materially from those anticipated in such forward- looking statements as a result of these risks and uncertainties, which include, without limitation, risks related to the ability of Armata's lead clinical candidates, AP-PA02 and AP-SA02, to be more effective than previous candidates; that the top line results are indicative of the final data; Armata's ability to expedite development of AP-PA02 and AP-SA02; Armata's ability to advance its preclinical and clinical programs and the uncertain and time-consuming regulatory approval process; Armata's ability to develop products based on bacteriophages and synthetic phages to kill bacterial pathogens; the Company's expected market opportunity for its products; Armata's ability to sufficiently fund its operations as expected, including obtaining additional funding as needed; and any delays or adverse events within, or outside of, Armata's control, caused by the ongoing COVID-19 pandemic. 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 16, 2023, 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.
LifeSci Advisors, LLC
Armata Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets
September 30, 2023 December 31, 2022
Assets
Current assets
Cash and cash equivalents $ 23,958,000 $ 14,852,000
Prepaid expenses 4,130,000 3,664,000
Other receivables 8,497,000 8,531,000
Total current assets 36,585,000 27,047,000
Property and equipment, net 9,250,000 3,617,000
Operating lease right-of-use asset 44,886,000 43,035,000
Intangible assets, net 13,746,000 13,746,000
Other long term assets 8,294,000 8,389,000
Total assets $ 112,761,000 $ 95,834,000
Liabilities and shareholders' (deficit) equity
Total current liabilities $ 21,884,000 $ 24,873,000
Long term debts 72,024,000 -
Other long term liabilities 28,162,000 31,804,000
Deferred tax liability 3,077,000 3,077,000
Total liabilities 125,147,000 59,754,000
Shareholders' (deficit) equity (12,386,000) 36,080,000
Total liabilities and shareholders' (deficit) equity $ 112,761,000 $ 95,834,000
Armata Pharmaceuticals, Inc.
Condensed Consolidated Statements of Operations
Three Months Ended Nine Months Ended
September 30, September 30,
2023 2022 2023 2022
Grant revenue $ 1,225,000 $ 1,338,000 $ 3,001,000 $ 4,457,000
Operating expenses:
Research and development 7,978,000 8,400,000 25,842,000 25,448,000
General and administrative 3,583,000 1,561,000 8,470,000 5,627,000
Total operating expenses 11,561,000 9,961,000 34,312,000 31,075,000
Loss from operations (10,336,000) (8,623,000) (31,311,000) (26,618,000)
Other income (expense), net (1,129,000) 9,000 (1,065,000) 15,000
Change in fair value of convertible debt (15,833,000) - (12,959,000) -
Loss on convertible debt extinguishment (3,863,000) - (3,863,000) -
Loss before income taxes and net loss $ (31,161,000) $ (8,614,000) $ (49,198,000) $ (26,603,000)
Net loss per share, basic and diluted $ (0.86) $ (0.24) $ (1.36) $ (0.79)
Weighted average shares outstanding, basic and diluted 36,086,990 36,038,686 36,067,025 33,704,071
Armata Pharmaceuticals, Inc.
Condensed Consolidated Statements of Cash Flows
Nine Months Ended September 30,
2023 2022
Operating activities:
Net loss $ (49,198,000) $ (26,603,000)
Adjustments required to reconcile net loss to net cash used in operating activities:
Depreciation and amortization expense 679,000 647,000
Share-based compensation expense 745,000 2,288,000
Change in fair value of convertible debt 12,959,000 -
Non-cash interest expense 1,176,000 -
Loss on convertible debt extinguishment 3,863,000 -
Change in right-of-use asset 662,000 1,215,000
Changes in operating assets and liabilities: (10,203,000) 457,000
Net cash used in operating activities (39,317,000) (21,996,000)
Investing activities:
Purchases of property and equipment (5,744,000) (2,666,000)
Net cash used in investing activities (5,744,000) (2,666,000)
Financing activities:
Proceeds from issuance of convertible debt, net of issuance costs 29,101,000 -
Proceeds from issuance of long-term debt, net of issuance costs 24,925,000 -
Proceeds from sale of common stock, net of offering costs - 44,391,000
Proceeds from exercise of stock options 5,000 125,000
Net cash provided by financing activities 54,031,000 44,516,000
Net increase in cash, cash equivalents and restricted cash 8,970,000 19,854,000
Cash, cash equivalents and restricted cash, beginning of period 20,812,000 11,488,000
Cash, cash equivalents and restricted cash, end of period $ 29,782,000 $ 31,342,000
Nine Months Ended September 30,
2023 2022
Cash and cash equivalents $ 23,958,000 $ 25,382,000
Restricted cash 5,824,000 5,960,000
Cash, cash equivalents and restricted cash $ 29,782,000 $ 31,342,000

Frequently Asked Questions

What significant progress did Armata Pharmaceuticals achieve in Q3 2023?

Armata reported accelerating enrollment in their Phase 2a diSArm study and Tailwind study, focusing on developing bacteriophage therapeutics for bacterial infections.

What is the role of the Department of Defense in Armata's developments?

The Department of Defense is financially supporting the development of AP-SA02, aimed at treating S. aureus bacteremia.

How much cash did Armata hold by September 2023?

As of September 30, 2023, Armata had approximately $24.0 million in unrestricted cash and equivalents.

What were Armata's research and development expenses in Q3 2023?

Armata's research and development expenses for Q3 2023 were approximately $8.0 million.

What is the expected completion timeline for Armata's Phase 2 studies?

Armata anticipates completing the Phase 2 studies for AP-SA02 and AP-PA02 in 2024.

Last updated: Nov 14, 2023