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Armata Pharmaceuticals

Armata Pharmaceuticals logo
🇺🇸United States
Ownership
Public, Subsidiary
Established
2005-01-01
Employees
66
Market Cap
$87M
Website
http://www.armatapharma.com
Introduction

Armata Pharmaceuticals, Inc. operates as a clinical-stage biotechnology company, which focuses on the development of bacteriophage therapeutics for the treatment of drug-resistant bacterial infections. The company was founded in 1989 and is headquartered in Los Angeles, CA.

Clinical Trials

13

Active:0
Completed:11

Trial Phases

2 Phases

Phase 1:3
Phase 2:8

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (11 trials with phase data)• Click on a phase to view related trials

Phase 2
8 (72.7%)
Phase 1
3 (27.3%)

Study to Evaluate the Safety, Phage Kinetics, and Efficacy of Inhaled AP-PA02 in Subjects With Non-Cystic Fibrosis Bronchiectasis and Chronic Pulmonary Pseudomonas Aeruginosa Infection

Phase 2
Completed
Conditions
Lung Infection
Non-cystic Fibrosis Bronchiectasis
Pseudomonas Aeruginosa
First Posted Date
2022-11-15
Last Posted Date
2024-08-14
Lead Sponsor
Armata Pharmaceuticals, Inc.
Target Recruit Count
48
Registration Number
NCT05616221
Locations
🇺🇸

Velocity Clinical Research, Mobile, Alabama, United States

🇺🇸

Southern California Institute for Respiratory Diseases Cedars-Sinai West Tower, Los Angeles, California, United States

🇺🇸

UCONN Health, Farmington, Connecticut, United States

and more 20 locations

Study Evaluating Safety, Tolerability, and Efficacy of Intravenous AP-SA02 in Subjects with S. Aureus Bacteremia

Phase 1
Completed
Conditions
Bacteremia
Bacteremia Staph
Staphylococcus Aureus
Bacteremia Due to Staphylococcus Aureus
Staphylococcus Aureus Bacteremia
Interventions
Other: Placebo
First Posted Date
2022-01-11
Last Posted Date
2025-03-26
Lead Sponsor
Armata Pharmaceuticals, Inc.
Target Recruit Count
50
Registration Number
NCT05184764
Locations
🇺🇸

Banner University Medical Center, Tucson, Arizona, United States

🇺🇸

University of California, San Diego (UCSD) - Medical Center, La Jolla, California, United States

🇺🇸

University of Southern California Keck School of Medicine, Los Angeles, California, United States

and more 25 locations

Ph 1/2 Study Evaluating Safety and Tolerability of Inhaled AP-PA02 in Subjects With Chronic Pseudomonas Aeruginosa Lung Infections and Cystic Fibrosis

Phase 1
Completed
Conditions
Pseudomonas
Cystic Fibrosis
Pseudomonas Aeruginosa
Lung Infection
Lung Infection Pseudomonal
First Posted Date
2020-10-22
Last Posted Date
2024-01-31
Lead Sponsor
Armata Pharmaceuticals, Inc.
Target Recruit Count
29
Registration Number
NCT04596319
Locations
🇺🇸

Children's Hospital Los Angeles, Los Angeles, California, United States

🇺🇸

University of South Florida, Tampa, Florida, United States

🇺🇸

St. Luke's Cystic Fibrosis Center of Idaho, Boise, Idaho, United States

and more 17 locations
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News

Armata's Bacteriophage Therapy Shows Promising Results in Treating Staphylococcus aureus Bacteremia

Armata Pharmaceuticals' Phase 1b/2a diSArm trial demonstrated that AP-SA02, a novel intravenous bacteriophage therapy, met all primary endpoints for safety, tolerability, and clinical response in complicated Staphylococcus aureus bacteremia.

Non-Cystic Fibrosis Bronchiectasis Market Expected to Reach USD 7.5 Billion by 2035, Driven by Novel Therapies

The Non-Cystic Fibrosis Bronchiectasis (NCFB) market is projected to grow from USD 1.7 billion in 2024 to USD 7.5 billion by 2035, representing a robust CAGR of 14.62%.

Phage Therapies and Novel Molecules Show Promise in Treating Chronic Pseudomonas Aeruginosa Pulmonary Infections

• Armata Pharmaceuticals' AP-PA02, a therapeutic phage cocktail, is currently in Phase II trials for bronchiectasis and pseudomonal infections, targeting *P. aeruginosa* in respiratory infections. • BiomX's BX004, a phage therapy, is in Phase I/II trials for chronic *Pseudomonas aeruginosa* pulmonary infections in cystic fibrosis patients, demonstrating activity against antibiotic-resistant strains. • The pipeline for chronic *Pseudomonas aeruginosa* pulmonary infections includes over 12 drugs in various stages of clinical development, with companies like Gilead and Respirion also involved.

NCFB Pipeline Shows Promise with Over 15 Companies Developing New Therapies

• The non-cystic fibrosis bronchiectasis (NCFB) market is experiencing growth due to rising prevalence and increased awareness, leading to early diagnosis and treatment. • Over 15 companies are actively developing more than 15 NCFB drugs, aiming to improve the treatment landscape for this chronic lung condition. • Key players like Insmed, AstraZeneca, and Verona Pharma are advancing promising therapies such as brensocatib, benralizumab and ensifentrine through clinical trials. • Recent clinical trial milestones, including Phase III results for brensocatib and Phase II enrollment for AP-PA02, signal progress in addressing unmet needs in NCFB treatment.

Iovance's MDA-TIL Trial Terminated, Sention's ST-1891 Phase II Completed

Iovance Biotherapeutics' MDA-TIL Phase II trial was terminated due to lack of efficacy, significantly decreasing its Phase Transition Success Rate (PTSR) in ovarian, colorectal, and pancreatic cancers.

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