Armata Pharmaceuticals, INC 8-K filings

Current reports — the filing a company makes when something happens that shareholders need to know about before the next quarterly report.

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Armata Pharmaceuticals announced significant progress in clinical, regulatory, and manufacturing for its AP-SA02 phage therapy, supporting a planned Phase 3 study initiation in late 2026.
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Armata Pharmaceuticals announced the promotion of David House to Chief Financial Officer and updated employment terms for Pierre Kyme, effective July 17, 2026.
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Armata Pharmaceuticals announced it has received agreement from the FDA on an Initial Pediatric Study Plan for AP-SA02, a key regulatory step for its Staphylococcus aureus bacteremia treatment.
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Armata Pharmaceuticals has appointed Dr. Daniel Gilmer to its Nominating and Corporate Governance Committee.
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Armata Pharmaceuticals shareholders re-elected seven board members and ratified the appointment of Ernst & Young LLP.
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Armata Pharmaceuticals announced a $25 million secured credit agreement with Innoviva and reported its first quarter 2026 financial results, highlighting progress on its lead therapeutic candidate AP-SA02.
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Armata Pharmaceuticals announced its intravenously administered Staphylococcus aureus multi-phage product candidate, AP-SA02, has received U.S. FDA Fast Track Designation for adjunct treatment of complicated bacteremia.
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Armata Pharmaceuticals announced the appointment of Dr. Daniel Gilmer to its Board of Directors, effective April 24, 2026.
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Armata Pharmaceuticals has scheduled its 2026 annual meeting of stockholders for June 11, 2026.
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Armata Pharmaceuticals announced its fourth quarter and full-year 2025 financial results, reporting a significant net loss and an audit opinion raising going concern doubts.
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Armata Pharmaceuticals announced a delay in its Q4 and full-year 2025 financial results while providing significant updates on its lead bacteriophage therapeutic, AP-SA02.
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Armata Pharmaceuticals announced its AP-SA02 product candidate received FDA Qualified Infectious Disease Product designation for complicated S. aureus bacteremia, offering significant development incentives.
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Armata Pharmaceuticals, Inc. has secured extensions for its credit agreements, outstanding warrants, and a voting agreement with principal shareholder Innoviva Strategic Opportunities LLC.
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Armata Pharmaceuticals announced FDA agreement to advance its AP-SA02 bacteriophage product into a Phase 3 superiority study for complicated Staphylococcus aureus bacteremia, marking a significant milestone for phage therapy.
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Armata Pharmaceuticals, Inc. has entered into a Capital on Demand Sales Agreement to offer and sell up to $100 million of its common stock through an at-the-market offering program.
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Armata Pharmaceuticals announced its Q3 2025 financial results and positive Phase 2a clinical data for AP-SA02 in complicated S. aureus bacteremia.
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Armata Pharmaceuticals announced positive Phase 2a clinical trial results for its bacteriophage cocktail AP-SA02 in treating complicated Staphylococcus aureus bacteremia, paving the way for a pivotal Phase 3 study.
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Armata Pharmaceuticals presents positive clinical data for its bacteriophage therapies, AP-SA02 and AP-PA02, highlighting significant efficacy and safety in treating serious bacterial infections.
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Armata Pharmaceuticals secured a $15 million loan from Innoviva and announced positive Phase 1b/2a clinical trial results for its lead S. aureus therapeutic phage candidate, AP-SA02, alongside its second quarter 2025 financial results.
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Armata Pharmaceuticals, Inc. announced that its shareholders elected seven directors, approved executive compensation on an advisory basis, and ratified Ernst & Young LLP as its independent auditor at the Annual Meeting held on June 12, 2025.
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Armata Pharmaceuticals reports positive topline data from its Phase 1b/2a diSArm study of AP-SA02 in complicated Staphylococcus aureus bacteremia, showing improved clinical outcomes.
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Armata Pharmaceuticals reported its Q1 2025 financial results, highlighting progress in clinical trials and securing additional funding.
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Armata Pharmaceuticals receives $4.65 million in additional non-dilutive funding from the Department of Defense to advance its AP-SA02 clinical trial for Staphylococcus aureus bacteremia.
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Armata Pharmaceuticals announces the date for its 2025 annual meeting of stockholders and related deadlines for stockholder proposals and director nominations.
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Armata Pharmaceuticals reports encouraging Phase 2 results for AP-PA02 and secures a $10 million credit agreement to advance its bacteriophage therapeutics.
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Armata Pharmaceuticals has entered into a $10 million secured credit agreement with Innoviva Strategic Opportunities LLC to further the development of its bacteriophage therapeutics.
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Armata Pharmaceuticals reports encouraging topline results from its Phase 2 Tailwind study, demonstrating a significant reduction of Pseudomonas aeruginosa in the lungs of non-cystic fibrosis bronchiectasis patients using inhaled AP-PA02.
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Armata Pharmaceuticals has finalized a separation agreement with its former Chief Medical Officer, Mina Pastagia, M.D., following her departure in November.
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Armata Pharmaceuticals has extended its debt maturity dates to January 10, 2026, and appointed new leadership in finance and regulatory strategy as it prepares for Phase 3 clinical trials.
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Armata Pharmaceuticals reported third quarter 2024 financial results and provided a corporate update, highlighting the completion of enrollment in two key clinical trials and securing additional funding.