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Armata Pharmaceuticals Announces Second Quarter 2023 Results and Provides Corporate Update

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Armata Pharmaceuticals announces Q2 2023 financial results and corporate update
Positive
  • Entered into new credit agreement with Innoviva for $25 million
  • Anticipates initiating Phase 2a study of AP-SA02 in 3Q23
Negative
  • Loss from operations of $(9.6) million for Q2 2023
  • Decrease in cash and equivalents from $14.9 million to $12.5 million

LOS ANGELES, Aug. 14, 2023 /PRNewswire/ -- 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 second quarter ended June 30, 2023, and provided a corporate update.  

Second Quarter 2023 and Recent Developments:

  • Announced leadership transition whereby world‐renowned healthcare leader and former Innoviva Board member Dr. Deborah L. Birx has been appointed Armata's new Chief Executive Officer. Dr. Birx has also been appointed to Armata's Board of Directors;
  • Entered into new credit agreement with Innoviva, the Company's largest shareholder, for gross proceeds of $25 million, and executed an amendment to its existing senior convertible credit and security agreement with Innoviva, extending the maturity date to January 10, 2025;
  • Continued enrollment in the Phase 2 study ("Tailwind") of inhaled AP-PA02 in patients with non-cystic fibrosis bronchiectasis (NCFB) and chronic Pseudomonas aeruginosa respiratory infection;
  • Further analyzed clinical data from the SWARM-P.a. study with the goal of advancing AP-PA02 into a Phase 2b/3 registrational study in cystic fibrosis (CF) patients in 2024;
  • Completed enrollment as planned of the Phase 1b part of the Phase 1b/2a study of AP-SA02 in Staphylococcus aureus bacteremia ("diSArm"); Company anticipates initiating the Phase 2a part of the study in 3Q23;
  • Commenced feasibility analysis of enrolling AP-SA02 prosthetic joint infection (PJI) study subjects at current "diSArm" sites for potential dual use enrollment in Q3-Q4 2023;
  • Progressed the build-out of its new advanced biologics cGMP facility that will provide the company with the manufacturing capacity to pursue partnership opportunities while also executing late-stage trials; and,
  • Delivered an oral presentation on the Company's recently completed Phase 1b/2a SWARM-P.a. clinical trial at the 6th World Conference on Targeting Phage Therapy, which was held June 1-2, 2023, in Paris.

"I am pleased to report significant progress during the second quarter, as we continued to advance two critical pathway clinical studies while preparing to initiate a third," stated Dr. Deborah Birx, Chief Executive Officer. "For AP-PA02, our five-phage cocktail targeting Pseudomonas aeruginosa, we continue to analyze results from our SWARM-P.a. study with the goal of progressing to a Phase 2b/3 registrational study in adult cystic fibrosis patients in 2024. At the same time, we have incorporated important learnings from this study into our ongoing Phase 2 trial of AP-PA02 in patients with non-cystic fibrosis bronchiectasis."

"Regarding our second clinical candidate, AP-SA02, we are concluding the Phase 1b part of our Staphylococcus aureus complicated bacteremia study in partnership with the U.S. Department of Defense, with plans to initiate the Phase 2a part this quarter.  We are excited to observe that the phage cocktail is well tolerated every six hours intravenously, opening the door to direct clinical evidence from the Phase 2a part and the potential for an accelerated 2b/3 registrational study.  Based on AP-SA02's favorable tolerability profile, we are in parallel advancing start-up activities for a second trial that will evaluate this cocktail as a potential treatment for S. aureus prosthetic joint infections." 

"I am pleased with our progress to date, and, with our strengthened balance sheet, laser focus, and clearly defined strategy, we look forward to a productive back half of the year as we work towards introducing phage therapy as a much-needed novel treatment for a broad range of dangerous, drug-resistant pathogens," Dr. Birx concluded.   

Second Quarter 2023 Financial Results

Grant Revenue. The Company recognized grant revenue of approximately $1.0 million for the three months ended June 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 $1.9 million of revenue in the comparable period in 2022.

Research and Development. Research and development expenses for the three months ended June 30, 2023 were approximately $8.3 million as compared to approximately $9.0 million for the comparable period in 2022. The Company continues to invest in clinical trial and personnel related expenses associated with its primary development programs.

General and Administrative. General and administrative expenses for the three months ended June 30, 2023 were approximately $2.4 million as compared to approximately $2.1 million for the comparable period in 2022. The increase was primarily related to expenses related to the increased legal and professional expenses.

Loss from Operations. Loss from operations for the three months ended June 30, 2023 was $(9.6) million as compared to a loss from operations of approximately $(9.2) million for the comparable period in 2022.

Cash and Equivalents. As of June 30, 2023, Armata held approximately $12.5 million of unrestricted cash and cash equivalents, as compared to $14.9 million as of December 31, 2022. Subsequent to the end of the second quarter, Armata announced a new credit agreement with Innoviva for gross proceeds totaling $25 million.   

As of August 8, 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 GMP 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.

Media Contacts:

At Armata:
Pierre Kyme
Armata Pharmaceuticals, Inc.
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

(Unaudited)










June 30, 2023


December 31, 2022







Assets














  Cash and cash equivalents


$

12,456,000


$

14,852,000

  Prepaid expenses



5,745,000



3,664,000

  Other receivable



8,633,000



8,531,000

Total current assets



26,834,000



27,047,000

Property and equipment, net



8,807,000



3,617,000

Operating lease right-of-use assets



43,652,000



43,035,000

Other long term assets



8,173,000



8,389,000

Intangible assets, net



13,746,000



13,746,000








Total assets


$

101,212,000


$

95,834,000








Liabilities and shareholders' equity







Convertible debt


$

26,352,000


$

-

Other current liabilities



25,210,000



24,873,000

Total current liabilities



51,562,000



24,873,000

Long term liabilities



27,430,000



31,804,000

Deferred tax liability



3,077,000



3,077,000

Total liabilities



82,069,000



59,754,000

Shareholders' equity



19,143,000



36,080,000

Total liabilities and shareholders' equity


$

101,212,000


$

95,834,000

 

Armata Pharmaceuticals, Inc

Condensed Consolidated Statements of Operations
















Three Months Ended June 30,


Six Months Ended June 30,



2023


2022


2023


2022



(Unaudited)


(Unaudited)


(Unaudited)


(Unaudited)














Grant Revenue


$

980,000


$

1,883,000


$

1,776,000


$

3,119,000

Operating expenses:













Research and development



8,259,000



9,020,000



17,863,000



17,048,000

General and administrative



2,350,000



2,083,000



4,888,000



4,066,000

Total operating expenses



10,609,000



11,103,000



22,751,000



21,114,000

Loss from operations



(9,629,000)



(9,220,000)



(20,975,000)



(17,995,000)

Other income (expense), net



46,000



5,000



64,000



6,000

Change in fair value of convertible debt



6,036,000



-



2,874,000



-

Loss before income taxes and Net Loss


$

(3,547,000)


$

(9,215,000)


$

(18,037,000)


$

(17,989,000)

Net loss per share, basic


$

(0.10)


$

(0.26)


$

(0.50)


$

(0.55)

Weighted average shares outstanding, basic



36,068,130



35,999,642



36,056,649



32,517,416

Net loss per share, diluted


$

(0.17)


$

(0.26)


$

(0.50)


$

(0.55)

Weighted average shares outstanding, diluted



56,544,698



35,999,642



36,056,649



32,517,416

 

Armata Pharmaceuticals, Inc


Condensed Consolidated Statements of Cash Flows












Six Months Ended June 30,




2023


2022








Operating activities:








Net loss


$

(18,037,000)


$

(17,989,000)


Adjustments required to reconcile net loss to net cash used in operating activities:








Share-based compensation



1,118,000



1,442,000


Depreciation



458,000



421,000


Change in fair value of convertible debt



(2,874,000)



-


Changes in operating assets and liabilities, net



(10,295,000)



4,463,000


Net cash used in operating activities



(29,630,000)



(11,663,000)


Investing activities:








Purchases of property and equipment, net



(2,232,000)



(1,372,000)


Net cash used in investing activities



(2,232,000)



(1,372,000)


Financing activities:








Proceeds from issuance of convertible debt, net



29,226,000



-


Proceeds from sale of common shares, net of offering costs



-



44,414,000


Proceeds from exercise of warrants and share-based options



-



71,000


Net cash provided by (used in) financing activities



29,226,000



44,485,000


Net increase (decrease) in cash and cash equivalents



(2,636,000)



31,450,000


Cash, cash equivalents and restricted cash, beginning of period



20,812,000



11,488,000


Cash, cash equivalents and restricted cash, end of period


$

18,176,000


$

42,938,000


























Reconciliation of Cash and cash equivalents:



Six Months Ended June 30,




2023


2022

Cash and cash equivalents


$

12,456,000


$

36,978,000


Restricted cash



5,720,000



5,960,000


Cash, cash equivalents and restricted cash


$

18,176,000


$

42,938,000


 

 

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SOURCE Armata Pharmaceuticals, Inc.

Armata Pharmaceuticals, Inc.

NYSE:ARMP

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Biotechnology
Biological Products, (no Disgnostic Substances)
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United States of America
LOS ANGELES