Developer docs
API playgroundTry for free, no card

Search company profiles

Armata Pharmaceuticals

Full company profile

uuid0003lki

Namestring
Armata Pharmaceuticals
Legal namestring
Armata Pharmaceuticals, Inc.
Company typeenum
Public
Founded yearint
2019
Descriptiontext

Armata Pharmaceuticals, Inc. (NYSE American: ARMP) is a late clinical-stage biotechnology company developing high-purity, pathogen-specific bacteriophage therapeutics to treat antibiotic-resistant bacterial infections in humans. The company's lead clinical candidate, AP-SA02, is a fixed multi-phage cocktail administered intravenously as adjunct therapy for complicated Staphylococcus aureus bacteremia caused by MSSA or MRSA; AP-SA02 demonstrated an 88% clinical response rate at day 12 versus 58% for placebo with zero relapse in the treatment arm in the Phase 2a diSArm study, and is positioned to enter a pivotal Phase 3 superiority study in H2 2026 after receiving FDA Fast Track Designation and Qualified Infectious Disease Product (QIDP) status. A second program, AP-PA02, targets Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-cystic fibrosis bronchiectasis patients, with related candidate AP-PA03 in earlier development. Underlying the pipeline is a proprietary synthetic phage platform supported by published cryo-EM structural biology work (collaboration with University of Alabama at Birmingham, published in Communications Biology / Nature Portfolio) and a 56,000 square foot in-house cGMP manufacturing facility in Los Angeles commissioned in November 2025.

The company is pre-commercial and generates no product revenue; its operating revenue consists of grant and award income (notably $1.1 million in Q1 2026 from the Medical Technology Enterprise Consortium), while development is funded primarily through non-dilutive U.S. Department of Defense awards totaling $28.7 million through MTEC and a series of secured credit facilities from its majority owner Innoviva Strategic Opportunities LLC totaling over $130 million since 2020, including a $25 million facility executed in May 2026 maturing January 2029. Armata was formed in 2019 through the merger involving AmpliPhi Biosciences, is incorporated in Delaware with operational headquarters in Los Angeles and Marina del Rey, California, is led by CEO Dr. Deborah L. Birx (appointed July 2023), and serves an eventual patient population of hospitalized S. aureus bacteremia cases and chronic respiratory infection sufferers with high unmet need given rising antimicrobial resistance.

Short descriptiontext

Armata Pharmaceuticals is a late clinical-stage biotechnology company developing high-purity bacteriophage therapeutics for antibiotic-resistant bacterial infections, advancing lead candidate AP-SA02 for Staphylococcus aureus bacteremia and AP-PA02 for Pseudomonas aeruginosa respiratory infections in cystic fibrosis patients.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersMarina Del Rey, United States
HQ citystring
Marina Del Rey
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bacteriophage therapeutics, antibiotic-resistant infections, clinical-stage biotechnology, phage cocktail therapeutics, infectious disease biologics
Industry4 codes
1Infectious Disease Specialty Pharmaceuticals (Non-vaccine)
CodeHLAIACAMPrimaryYes
2Infectious Disease & Antimicrobials Pharmaceuticals
CodeHLAIAAAGPrimaryNo
3Regulatory Strategy & IND/NDA/BLA Submissions Support
CodeHLAIALAHPrimaryNo
4Microbiome Modulating Small Molecules & Antibiotic Alternatives
CodeHLAAAFAGPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biopharmaceutical Therapeutics
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Grant and Award Revenue
TypeData Monetisation
Description

Armata generates grant and award revenue from government and non-governmental sources. The company recognized $0.8 million in Q1 2026 from Medical Technology Enterprise Consortium cost-sharing for the AP-SA02 program. Historically, the company has received substantial non-dilutive funding from the U.S. Department of Defense for clinical development.

investor.armatapharma.com
2Pharmaceutical Product Sales (Future)
TypeLicensing Royalties
Description

Pre-commercial stage. The company is advancing bacteriophage therapeutics through clinical development toward regulatory approval. If approved, AP-SA02 and AP-PA02 would be commercialized as prescription biologics for treatment of antibiotic-resistant bacterial infections, generating product revenue through standard pharmaceutical distribution channels.

investor.armatapharma.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Infrastructure, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Armata Pharmaceuticals develops high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant bacterial infections. Its lead clinical candidate, AP-SA02, is a multi-phage cocktail administered intravenously for complicated Staphylococcus aureus bacteremia (including MRSA) and is advancing toward a Phase 3 superiority study. A second candidate, AP-PA02, targets Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-CF bronchiectasis patients. The company supports its pipeline with proprietary synthetic phage engineering technology and an in-house 56,000 sq ft cGMP manufacturing facility in Los Angeles.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 88% clinical response rate at day 12 for AP-SA02 vs 58% for placebo in Phase 2a diSArm study
+1 more record
Product overview1 text field

Armata Pharmaceuticals is a late clinical-stage biotechnology company developing a pipeline of high-purity, pathogen-specific bacteriophage therapeutics for treating antibiotic-resistant bacterial infections. The company's product portfolio includes clinical candidates AP-SA02 (for Staphylococcus aureus bacteremia) and AP-PA02 (for Pseudomonas aeruginosa respiratory infections), along with manufacturing capabilities including a cGMP facility in Los Angeles. The company operates a proprietary bacteriophage-based technology platform using both natural and synthetic phage candidates.

Product and service4 records
1AP-SA02
CategoryClinical-stage bacteriophage therapeutic candidate
Description

Fixed multi-phage cocktail administered intravenously as adjunct treatment of complicated Staphylococcus aureus bacteremia caused by MSSA or MRSA; advancing toward Phase 3 superiority study after FDA End-of-Phase 2 alignment and QIDP and Fast Track designations.

2AP-PA02
CategoryClinical-stage bacteriophage therapeutic candidate
Description

Therapeutic phage cocktail targeting Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-CF bronchiectasis patients; includes phage P7-1 structurally characterized in collaboration with the University of Alabama at Birmingham.

3AP-PA03
CategoryPipeline bacteriophage therapeutic candidate
Description

Pipeline candidate related to the AP-PA02 program for Pseudomonas aeruginosa infections, part of Armata's pipeline of natural and synthetic phage candidates.

4cGMP Phage Manufacturing Facility
CategoryBiologics manufacturing capability
Description

State-of-the-art 56,000 square foot cGMP manufacturing facility in Los Angeles with clean rooms and quality control laboratories, producing high-purity bacteriophage therapeutics for clinical trials and potential commercialization.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-04
Description

Research collaboration with University of Alabama at Birmingham for structural characterization of phage P7-1, a component of the AP-PA02 phage cocktail. The study used cryo-electron microscopy to reveal phage architecture and has been published in Communications Biology (Nature Portfolio). This collaboration supports Armata's understanding of phage structure for engineering next-generation therapeutics.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage company developing engineered bacteriophage products enhanced with CRISPR-Cas3 to target antibiotic-resistant pathogens — directly comparable in modality (engineered phage) and infectious-disease focus to Armata's pipeline.

TypeDirect peer
Description

Clinical-stage phage therapy company developing customized phage cocktails for chronic infections and microbiome-related diseases — comparable in phage-cocktail approach and infectious-disease focus, with both natural and engineered phage candidates.

TypeDirect peer
Description

Clinical-stage phage-based biotherapeutics company developing products for antibiotic-resistant bacterial infections — directly comparable modality and therapeutic focus to Armata, with parallel pipeline approach.

TypeBroad incumbent
Description

Clinical-stage anti-infectives company developing immunotherapy-based approaches (Cloudbreak) and traditional antivirals/antifungals for serious infections — a broader anti-infectives peer with similar small-cap clinical-stage profile and FDA designation history.

TypeDirect peer
Description

Commercial-stage phage technology company producing phage-based products for food safety, animal health, and human therapeutics — a peer in the broader bacteriophage space, though with a more diversified commercial focus than Armata's pure-play anti-infectives strategy.

TypeBroad incumbent
Description

Commercial/clinical-stage anti-infectives company with approved antibiotic (XENLETA) for community-acquired bacterial pneumonia — a broader incumbent in the anti-infectives space with comparable size profile and target indications (serious bacterial infections).

TypeDirect peer
Description

Developer of engineered phage-based precision medicines (Eligobiotics) for microbiome modulation and infectious disease — a direct phage-therapeutics peer, though earlier-stage than Armata, with overlapping technology approach.

TypeDirect peer
Description

Clinical-stage bacteriophage therapy company developing phage-based treatments for antibiotic-resistant infections, including S. aureus and P. aeruginosa — the most directly comparable peer to Armata given overlapping targets and modality.

TypeBroad incumbent
Description

Clinical-stage anti-infectives company developing oral and IV antibiotics for multi-drug resistant infections — comparable as a small-cap anti-infectives peer targeting similar hospital-treated resistant infections, though via traditional small-molecule approach rather than phage.

TypeOthers
Description

Anti-infectives company developing targeted small-molecule antibiotics for drug-resistant infections, acquired by Innoviva in 2022 — a sibling entity under Armata's controlling shareholder, providing relevant peer benchmarks for anti-infectives development and Innoviva's broader strategic portfolio.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds17 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors8 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Armata Pharmaceuticals

Biopharmaceutical Therapeuticsarmatapharma.com

Armata Pharmaceuticals is a late clinical-stage biotechnology company developing high-purity bacteriophage therapeutics for antibiotic-resistant bacterial infections, advancing lead candidate AP-SA02 for Staphylococcus aureus bacteremia and AP-PA02 for Pseudomonas aeruginosa respiratory infections in cystic fibrosis patients.

What Armata Pharmaceuticals does

Armata Pharmaceuticals, Inc. (NYSE American: ARMP) is a late clinical-stage biotechnology company developing high-purity, pathogen-specific bacteriophage therapeutics to treat antibiotic-resistant bacterial infections in humans. The company's lead clinical candidate, AP-SA02, is a fixed multi-phage cocktail administered intravenously as adjunct therapy for complicated Staphylococcus aureus bacteremia caused by MSSA or MRSA; AP-SA02 demonstrated an 88% clinical response rate at day 12 versus 58% for placebo with zero relapse in the treatment arm in the Phase 2a diSArm study, and is positioned to enter a pivotal Phase 3 superiority study in H2 2026 after receiving FDA Fast Track Designation and Qualified Infectious Disease Product (QIDP) status. A second program, AP-PA02, targets Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-cystic fibrosis bronchiectasis patients, with related candidate AP-PA03 in earlier development. Underlying the pipeline is a proprietary synthetic phage platform supported by published cryo-EM structural biology work (collaboration with University of Alabama at Birmingham, published in Communications Biology / Nature Portfolio) and a 56,000 square foot in-house cGMP manufacturing facility in Los Angeles commissioned in November 2025.

The company is pre-commercial and generates no product revenue; its operating revenue consists of grant and award income (notably $1.1 million in Q1 2026 from the Medical Technology Enterprise Consortium), while development is funded primarily through non-dilutive U.S. Department of Defense awards totaling $28.7 million through MTEC and a series of secured credit facilities from its majority owner Innoviva Strategic Opportunities LLC totaling over $130 million since 2020, including a $25 million facility executed in May 2026 maturing January 2029. Armata was formed in 2019 through the merger involving AmpliPhi Biosciences, is incorporated in Delaware with operational headquarters in Los Angeles and Marina del Rey, California, is led by CEO Dr. Deborah L. Birx (appointed July 2023), and serves an eventual patient population of hospitalized S. aureus bacteremia cases and chronic respiratory infection sufferers with high unmet need given rising antimicrobial resistance.

Armata Pharmaceuticals firmographics

Firmographics
Name
Armata Pharmaceuticals
Legal name
Armata Pharmaceuticals, Inc.
Website
https://armatapharma.com
Company type
Public
Founded year
2019
Operating status
Operating
Headcount range
51–100 employees
Short description
Armata Pharmaceuticals is a late clinical-stage biotechnology company developing high-purity bacteriophage therapeutics for antibiotic-resistant bacterial infections, advancing lead candidate AP-SA02 for Staphylococcus aureus bacteremia and AP-PA02 for Pseudomonas aeruginosa respiratory infections in cystic fibrosis patients.
Ownership category
akta.pro rank

Armata Pharmaceuticals industry classification

Industry
Product category
Biopharmaceutical Therapeutics
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Infectious Disease Specialty Pharmaceuticals (Non-vaccine) (HLAIACAM)
akta.pro secondary industries
Infectious Disease & Antimicrobials Pharmaceuticals (HLAIAAAG), Regulatory Strategy & IND/NDA/BLA Submissions Support (HLAIALAH), Microbiome Modulating Small Molecules & Antibiotic Alternatives (HLAAAFAG)

Keywords

  • Bacteriophage therapeutics
  • Antibiotic-resistant infections
  • Clinical-stage biotechnology
  • Phage cocktail therapeutics
  • Infectious disease biologics

Where Armata Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Marina Del Rey
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Armata Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Infrastructure, Marketing or Sales

Revenue model

  1. Grant and Award Revenue: Armata generates grant and award revenue from government and non-governmental sources. The company recognized $0.8 million in Q1 2026 from Medical Technology Enterprise Consortium cost-sharing for the AP-SA02 program. Historically, the company has received substantial non-dilutive funding from the U.S. Department of Defense for clinical development.
  2. Pharmaceutical Product Sales (Future): Pre-commercial stage. The company is advancing bacteriophage therapeutics through clinical development toward regulatory approval. If approved, AP-SA02 and AP-PA02 would be commercialized as prescription biologics for treatment of antibiotic-resistant bacterial infections, generating product revenue through standard pharmaceutical distribution channels.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Armata Pharmaceuticals product offering

Product offering

Core offering

Armata Pharmaceuticals develops high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant bacterial infections. Its lead clinical candidate, AP-SA02, is a multi-phage cocktail administered intravenously for complicated Staphylococcus aureus bacteremia (including MRSA) and is advancing toward a Phase 3 superiority study. A second candidate, AP-PA02, targets Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-CF bronchiectasis patients. The company supports its pipeline with proprietary synthetic phage engineering technology and an in-house 56,000 sq ft cGMP manufacturing facility in Los Angeles.

Product overview

Armata Pharmaceuticals is a late clinical-stage biotechnology company developing a pipeline of high-purity, pathogen-specific bacteriophage therapeutics for treating antibiotic-resistant bacterial infections. The company's product portfolio includes clinical candidates AP-SA02 (for Staphylococcus aureus bacteremia) and AP-PA02 (for Pseudomonas aeruginosa respiratory infections), along with manufacturing capabilities including a cGMP facility in Los Angeles. The company operates a proprietary bacteriophage-based technology platform using both natural and synthetic phage candidates.

Differentiator

Problem solved

Functional benefit

Products and services

  • AP-SA02 Fixed multi-phage cocktail administered intravenously as adjunct treatment of complicated Staphylococcus aureus bacteremia caused by MSSA or MRSA; advancing toward Phase 3 superiority study after FDA End-of-Phase 2 alignment and QIDP and Fast Track designations.
  • AP-PA02 Therapeutic phage cocktail targeting Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-CF bronchiectasis patients; includes phage P7-1 structurally characterized in collaboration with the University of Alabama at Birmingham.
  • AP-PA03 Pipeline candidate related to the AP-PA02 program for Pseudomonas aeruginosa infections, part of Armata's pipeline of natural and synthetic phage candidates.
  • cGMP Phage Manufacturing Facility State-of-the-art 56,000 square foot cGMP manufacturing facility in Los Angeles with clean rooms and quality control laboratories, producing high-purity bacteriophage therapeutics for clinical trials and potential commercialization.

Quantifiable outcome

  • 88% clinical response rate at day 12 for AP-SA02 vs 58% for placebo in Phase 2a diSArm study
  • +1 more outcomes

Companies that use Armata Pharmaceuticals

Customer profile

Segments2 records

Ideal customer profiles3 records

Armata Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Armata Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • University of Alabama at BirminghamcoreStrategic or Co-development Partner · 4 May 2026Research collaboration with University of Alabama at Birmingham for structural characterization of phage P7-1, a component of the AP-PA02 phage cocktail. The study used cryo-electron microscopy to reveal phage architecture and has been published in Communications Biology (Nature Portfolio). This collaboration supports Armata's understanding of phage structure for engineering next-generation therapeutics.

Scale indicators8 records

Recent moves7 records

Expansion highlights5 records

Armata Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Locus Biosciences: Clinical-stage company developing engineered bacteriophage products enhanced with CRISPR-Cas3 to target antibiotic-resistant pathogens — directly comparable in modality (engineered phage) and infectious-disease focus to Armata's pipeline.
  • BiomX: Clinical-stage phage therapy company developing customized phage cocktails for chronic infections and microbiome-related diseases — comparable in phage-cocktail approach and infectious-disease focus, with both natural and engineered phage candidates.
  • Phagelux: Clinical-stage phage-based biotherapeutics company developing products for antibiotic-resistant bacterial infections — directly comparable modality and therapeutic focus to Armata, with parallel pipeline approach.
  • Intralytix: Commercial-stage phage technology company producing phage-based products for food safety, animal health, and human therapeutics — a peer in the broader bacteriophage space, though with a more diversified commercial focus than Armata's pure-play anti-infectives strategy.
  • Eligo Bioscience: Developer of engineered phage-based precision medicines (Eligobiotics) for microbiome modulation and infectious disease — a direct phage-therapeutics peer, though earlier-stage than Armata, with overlapping technology approach.
  • Adaptive Phage Therapeutics: Clinical-stage bacteriophage therapy company developing phage-based treatments for antibiotic-resistant infections, including S. aureus and P. aeruginosa — the most directly comparable peer to Armata given overlapping targets and modality.

Broad incumbents

  • Cidara Therapeutics: Clinical-stage anti-infectives company developing immunotherapy-based approaches (Cloudbreak) and traditional antivirals/antifungals for serious infections — a broader anti-infectives peer with similar small-cap clinical-stage profile and FDA designation history.
  • Nabriva Therapeutics: Commercial/clinical-stage anti-infectives company with approved antibiotic (XENLETA) for community-acquired bacterial pneumonia — a broader incumbent in the anti-infectives space with comparable size profile and target indications (serious bacterial infections).
  • Iterum Therapeutics: Clinical-stage anti-infectives company developing oral and IV antibiotics for multi-drug resistant infections — comparable as a small-cap anti-infectives peer targeting similar hospital-treated resistant infections, though via traditional small-molecule approach rather than phage.

Others

  • Entasis Therapeutics: Anti-infectives company developing targeted small-molecule antibiotics for drug-resistant infections, acquired by Innoviva in 2022 — a sibling entity under Armata's controlling shareholder, providing relevant peer benchmarks for anti-infectives development and Innoviva's broader strategic portfolio.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Armata Pharmaceuticals social profiles

Digital presence

Armata Pharmaceuticals compliance and trust

Trust signal

Compliance3 records

Armata Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Armata Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles10 records

Armata Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds17 records

Investors8 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Armata Pharmaceuticals M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Armata Pharmaceuticals

What does Armata Pharmaceuticals do?

Armata Pharmaceuticals develops high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant bacterial infections. Its lead clinical candidate, AP-SA02, is a multi-phage cocktail administered intravenously for complicated Staphylococcus aureus bacteremia (including MRSA) and is advancing toward a Phase 3 superiority study. A second candidate, AP-PA02, targets Pseudomonas aeruginosa respiratory infections in cystic fibrosis and non-CF bronchiectasis patients. The company supports its pipeline with proprietary synthetic phage engineering technology and an in-house 56,000 sq ft cGMP manufacturing facility in Los Angeles.

Is Armata Pharmaceuticals a public or private company?

Armata Pharmaceuticals is a public company. It is classified as public and is currently operating.

When was Armata Pharmaceuticals founded?

Armata Pharmaceuticals was founded in 2019. It employs 51 to 100 people.

Where is Armata Pharmaceuticals based?

Armata Pharmaceuticals is headquartered in Marina Del Rey, United States, in the North America region.

How does Armata Pharmaceuticals make money?

Two revenue lines are on record. Grant and Award Revenue is the primary driver. The others are pharmaceutical Product Sales (Future).

Who are Armata Pharmaceuticals's main competitors?

Direct peers on record are Locus Biosciences, BiomX, Phagelux, Intralytix, Eligo Bioscience and Adaptive Phage Therapeutics. Broad incumbents are Cidara Therapeutics, Nabriva Therapeutics and Iterum Therapeutics. Entasis Therapeutics is listed as an others.

Does Armata Pharmaceuticals have an API?

No public API is recorded for Armata Pharmaceuticals.

What industry is Armata Pharmaceuticals in?

Armata Pharmaceuticals's product category is Biopharmaceutical Therapeutics. Its primary akta.pro industry code is HLAIACAM, Infectious Disease Specialty Pharmaceuticals (Non-vaccine), with a secondary code of HLAIAAAG, Infectious Disease & Antimicrobials Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Investing.comArmata Pharmaceuticals receives two U.S. patents for therapiesArmata Pharmaceuticals received two U.S. patents for its bacteriophage programs AP-SA02 and AP-PA02, covering treatments for Staphylococcus aureus and Pseudomonas infections. The patents provide protection until 2041 and 2043, respectively, and AP-SA02 is in development for complicated bacteremia. The company plans to advance AP-SA02 into a Phase 3 superiority study in the second half of 2026.BenzingaArmata Pharmaceuticals Stock Slides after Pentagon Funding - Armata Pharmaceuticals (AMEX:ARMP)Armata Pharmaceuticals shares fell 10.95% to $3.74 on Wednesday after receiving $3.7 million in additional non-dilutive DoD funding for its AP-SA02 bacteriophage program. The funding brings cumulative DoD support to about $32.4 million, but the stock remains 21.2% below its 20-day moving average.AInvestArmata Pharmaceuticals (ARMP) Plunges 16%: A Technical Collapse Amidst Biotech VolatilityArmata Pharmaceuticals stock fell 16.22% to $4.65 on technical selling, breaking below key moving averages and testing the $4.49 Bollinger Band lower bound. The decline occurred despite a stable biotech sector, with Vertex down only 0.77%. A sustained hold above $4.50 is needed to confirm a technical bounce.AdvfnArmata Pharmaceuticals Shares Rise 8% After FDA Grants AP-SA02 Breakthrough Therapy DesignationArmata Pharmaceuticals shares rose 8% after the FDA granted Breakthrough Therapy designation to AP-SA02, its multi-phage product for complicated S. aureus bacteremia. The designation follows Phase 1b/2a data showing 100% of patients maintained clinical response versus 75% on placebo. AP-SA02 now holds three FDA designations.MarketScreenerArmata Pharma Shares Rise on FDA Breakthrough Therapy Designation for Antibacterial TreatmentArmata Pharmaceuticals shares rose 10% to $5.92 after the FDA granted breakthrough therapy designation for its antibacterial candidate AP-SA02. The designation expedites review of the intravenous treatment for complicated S. aureus bacteremia, with the company aiming to bring the therapy to patients quickly.Markets DailyHC Wainwright Forecasts Armata Pharmaceuticals Q3 EarningsHC Wainwright analysts lowered their Q3 2026 earnings per share estimates for Armata Pharmaceuticals to ($0.57) from a previous forecast of ($0.53). This revision follows the company's recent quarterly report where it beat consensus estimates for both EPS and revenue, posting $2.51 million in sales.PR NewswireArmata Pharmaceuticals Announces Financial Results for the Second Quarter 2026 and Provides a Corporate UpdateArmata Pharmaceuticals reported a net income of $74.1 million for the second quarter of 2026, driven primarily by a $91.0 million non-cash gain from the change in fair value of its Convertible Loan. The company also announced that it has submitted the Phase 3 protocol for its AP-SA02 bacteriophage therapeutic to the FDA and received Fast Track designation, with plans to initiate the pivotal study in the second half of 2026.YahooArmata Pharmaceuticals Announces Financial Results for the Second Quarter 2026 and Provides a Corporate UpdateArmata Pharmaceuticals announced its financial results for the second quarter of 2026 and provided a corporate update regarding its lead candidate, AP-SA02. The company submitted the Phase 3 superiority protocol to the FDA and received additional non-dilutive funding from the U.S. Department of War to support the study's initiation in the second half of 2026.Stock TitanArmata Q2 2026 Earnings: $74.1M Net IncomeArmata Pharmaceuticals reported a $74.1 million net income for the second quarter of 2026, driven primarily by a $91.0 million non-cash gain from the change in fair value of its Convertible Loan. The company also announced significant progress on its lead candidate AP-SA02, including FDA Fast Track designation and an agreement to initiate a pivotal Phase 3 study in the second half of 2026.Seeking AlphaInnoviva: The Royalty Decline Is Real, But The Valuation Is Too Pessimistic (NASDAQ:INVA)An analyst from Fair Value Desk has issued a buy rating for Innoviva Inc. (INVA) at its current price of ~$21, arguing the market is overly pessimistic about royalty revenue decline from GSK respiratory products. The analysis projects 68% upside to a base-case fair value of $36.92, citing strong growth in Innoviva Specialty Therapeutics (IST) products (37% YoY growth in Q1 2026, reaching $172.1M in 2025 net sales) which the author believes will offset royalty decline. Key risks identified include margin compression (gross margin fell from ~100% to 74.8%), Armata Pharmaceuticals strategic investment impairment risk ($773M in investments), and management's capital allocation decisions.