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Armata Pharmaceuticals Announces Structural Biology Publication

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Armata Pharmaceuticals (NYSE American: ARMP) announced a publication in Communications Biology describing the structure of phage Pa193, a key component of their multi-phage clinical candidate AP-PA02. The study, utilizing cryogenic electron microscopy, focuses on treating Pseudomonas aeruginosa infections in patients with cystic fibrosis (CF) or non-cystic fibrosis bronchiectasis (NCFB). The research provides detailed structural analysis at single atom resolution, offering insights into phage stability and genome-delivery mechanisms. This understanding could potentially expand clinical applications to other pathogens beyond P. aeruginosa.

Armata Pharmaceuticals (NYSE American: ARMP) ha annunciato una pubblicazione su Communications Biology che descrive la struttura del fago Pa193, un componente chiave del loro candidato clinico multi-fago AP-PA02. Lo studio, che utilizza la microscopia elettronica criogenica, si concentra sul trattamento delle infezioni da Pseudomonas aeruginosa in pazienti con fibrosi cistica (FC) o bronchiectasia non fibrotica (NCFB). La ricerca offre un'analisi strutturale dettagliata a risoluzione atomica singola, fornendo spunti sulla stabilità del fago e sui meccanismi di consegna del genoma. Questa comprensione potrebbe espandere potenzialmente le applicazioni cliniche ad altri patogeni oltre a P. aeruginosa.

Armata Pharmaceuticals (NYSE American: ARMP) anunció una publicación en Communications Biology que describe la estructura del fago Pa193, un componente clave de su candidato clínico multi-fago AP-PA02. El estudio, que utiliza microscopía electrónica criogénica, se centra en el tratamiento de infecciones por Pseudomonas aeruginosa en pacientes con fibrosis quística (FQ) o bronquiectasia no asociada a fibrosis quística (NCFB). La investigación proporciona un análisis estructural detallado a resolución de un solo átomo, ofreciendo perspectivas sobre la estabilidad del fago y los mecanismos de entrega del genoma. Este entendimiento podría expandir potencialmente las aplicaciones clínicas a otros patógenos más allá de P. aeruginosa.

Armata Pharmaceuticals (NYSE American: ARMP)는 Communications Biology에 파지 Pa193의 구조를 설명하는 발표를 했습니다. 이는 그들의 다중 파지 임상 후보 AP-PA02의 핵심 구성 요소입니다. 이 연구는 극저온 전자 현미경을 사용하여 치료하는 것을 중심으로 하며, 낭성 섬유증 (CF) 환자나 비낭성 섬유증 기관지 확장증 (NCFB) 환자의 Pseudomonas aeruginosa 감염을 목표로 합니다. 연구는 단일 원자 해상도에서의 자세한 구조 분석을 제공하며, 파지의 안정성과 유전체 전달 메커니즘에 대한 통찰력을 제공합니다. 이 이해는 P. aeruginosa 외의 다른 병원체에 대한 임상 응용 프로그램을 확장할 수 있는 잠재력을 가질 수 있습니다.

Armata Pharmaceuticals (NYSE American: ARMP) a annoncé une publication dans Communications Biology décrivant la structure du phage Pa193, un élément clé de leur candidat clinique multi-phage AP-PA02. L'étude, utilisant la microscopie électronique cryogénique, se concentre sur le traitement des infections à Pseudomonas aeruginosa chez des patients atteints de fibrose kystique (FK) ou de bronchiectasie non fibrosée (NCFB). La recherche fournit une analyse structurale détaillée à résolution atomique unique, offrant des éclairages sur la stabilité des phages et les mécanismes de livraison du génome. Cette compréhension pourrait potentiellement étendre les applications cliniques à d'autres agents pathogènes au-delà de P. aeruginosa.

Armata Pharmaceuticals (NYSE American: ARMP) gab die Veröffentlichung in Communications Biology bekannt, die die Struktur des Phagen Pa193 beschreibt, eines Schlüsselkomponenten ihres Multi-Phagen-Kandidaten AP-PA02. Die Studie, die Kryo-Elektronenmikroskopie nutzt, konzentriert sich auf die Behandlung von Pseudomonas aeruginosa-Infektionen bei Patienten mit zystischer Fibrose (CF) oder nichtzystischer Fibrose-Bronchiektasie (NCFB). Die Forschung bietet eine detaillierte strukturelle Analyse mit atomarer Auflösung und liefert Einblicke in die Stabilität des Phagen sowie in Mechanismen der Genomübertragung. Dieses Verständnis könnte potenziell die klinischen Anwendungen auf andere Krankheitserreger über P. aeruginosa hinaus erweitern.

Positive
  • Advanced understanding of phage Pa193 structure could lead to expanded therapeutic applications
  • Research progress supports development of clinical candidate AP-PA02
  • Successful structural analysis at single atom resolution demonstrates technological capability
Negative
  • None.

Insights

This structural biology publication, while scientifically interesting, has immediate impact on Armata Pharmaceuticals' business prospects or stock value. The study describes the atomic structure of phage Pa193, which is part of their clinical candidate AP-PA02, but doesn't provide new clinical data or regulatory progress.

The research demonstrates scientific capabilities and potentially aids future development, but lacks concrete advancement in the company's clinical pipeline. While it may help inform future therapeutic applications, there are no immediate catalysts for value creation. The publication primarily serves to build scientific credibility and understanding of their technology platform.

The involvement of notable researchers and publication in a Nature Portfolio journal adds academic prestige, but investors should focus more on upcoming clinical trial results and regulatory milestones for AP-PA02 in CF and NCFB indications.

Publication describes the structure of phage Pa193, a top candidate for inclusion into Armata's multi-phage anti-Pseudomonas clinical products

LOS ANGELES, Oct. 30, 2024 /PRNewswire/ -- Armata Pharmaceuticals, Inc. (NYSE American: ARMP) ("Armata" or the "Company"), a biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for antibiotic-resistant and difficult-to-treat bacterial infections, today announced a paper in Communications Biology, published by Nature Portfolio.

The publication, titled, "Cryo-EM analysis of Pseudomonas phage Pa193 structural components," describes the structure of phage Pa193. Pa193 is representative of a family of phages present in Armata's multi-phage clinical candidate, AP-PA02, which the company is developing to treat chronic Pseudomonas aeruginosa infections in patients with cystic fibrosis (CF) or non-cystic fibrosis bronchiectasis (NCFB).

"We are very pleased to simultaneously advance the fundamental understanding of phage structure while remaining laser focused on phage function in full clinical development. One of our phage clinical candidates contributed to the important learnings from this study," stated Dr. Deborah Birx, Chief Executive Officer of Armata. "As we continue to advance our proprietary development programs, which are founded on uncompromising science and rigorously designed clinical trials, this study furthers our understanding of phage structural components and how changes in phage biology may expand their clinical utility to other dangerous pathogens beyond P. aeruginosa, potentially informing future development plans." 

Dr. Gino Cingolani, Anderson Family Endowed Chair in Medical Education, Research & Patient Care and Professor in the Department of Biochemistry and Molecular Genetics, The University of Alabama at Birmingham, and co-author of the paper, stated, "This research highlights our ability to decipher a whole virus at the single atom resolution. Leveraging cryogenic electron microscopy, proteomics and bioinformatic analysis, we are now able to take a complete inventory of all structural components of a large macromolecular assembly, such as Pa193. The opportunities are endless. From a basic-science standpoint, understanding both the architecture and design principles of Pa193 provides valuable insight into its stability and mechanisms of genome-delivery. These findings can be generalized to other members of the Pa193 phage family and aid in structure prediction and protein engineering, valuable to using phages as biomedicines for therapeutic applications."

The full publication can be found here: https://www.nature.com/articles/s42003-024-06985-x

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
Armata Pharmaceuticals, Inc.
ir@armatapharma.com
310-665-2928 x234

Investor Relations:
Joyce Allaire
LifeSci Advisors, LLC
jallaire@lifesciadvisors.com
212-915-2569

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SOURCE Armata Pharmaceuticals, Inc.

FAQ

What is the purpose of Armata Pharmaceuticals' phage Pa193 study?

The study describes the structure of phage Pa193, which is part of Armata's multi-phage clinical candidate AP-PA02, being developed to treat Pseudomonas aeruginosa infections in CF and NCFB patients.

What technology was used in Armata's (ARMP) phage structure research?

The research utilized cryogenic electron microscopy, proteomics, and bioinformatic analysis to study the phage structure at single atom resolution.

What conditions is Armata Pharmaceuticals' AP-PA02 targeting?

AP-PA02 is being developed to treat chronic Pseudomonas aeruginosa infections in patients with cystic fibrosis (CF) or non-cystic fibrosis bronchiectasis (NCFB).

Armata Pharmaceuticals, Inc.

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