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Aqualung Therapeutics

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uuid0002ue6

Namestring
Aqualung Therapeutics
Legal namestring
Aqualung Therapeutics Corporation
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Aqualung Therapeutics Corporation is a clinical-stage immunotherapeutics company developing a platform of biologic therapies that target extracellular nicotinamide phosphoribosyltransferase (eNAMPT) and its downstream TLR4-mediated inflammatory signaling cascade. The company's lead asset, ALT-100 mAb, is a humanized monoclonal antibody designed to neutralize eNAMPT as an upstream master regulatory cytokine rather than downstream single cytokines, with the goal of interrupting unchecked inflammation and vascular leakage at their source. The pipeline also includes NTyP-100 (a novel nanocarrier delivery platform) and SELP-100 (a fusion immunoglobulin protein targeting SELPLG/P-selectin), together marketed as the eNamptor platform. Lead clinical programs are the PUERTA Phase 2a trial in acute respiratory distress syndrome (ARDS) and the PAISANO Phase 2a trial in progressive pulmonary fibrosis, with additional preclinical-stage exploration across radiation-induced lung injury, NASH, pulmonary hypertension, IBD, lupus vasculitis, prostate cancer, and chorioamnionitis-related preterm birth.

The company is pre-revenue and operates a biotech development model in which operating capital is sourced from a combination of NIH grant awards (STTR and other mechanisms) and venture financing. As of the most recent disclosures, total venture funding includes a $2.5 million convertible note round completed in January 2022, alongside multiple NIH awards. Pricing is not publicly disclosed because no product is commercialized; future revenue is expected to derive from biopharmaceutical product sales following FDA approval and from pharmaceutical licensing or partnership arrangements for global commercialization. The customer base consists of multiple end-market segments — critical care/ICU, pulmonology, radiation oncology, hepatology, rheumatology, gastroenterology, oncology, and obstetrics — but the company's effective near-term "customers" are academic collaborators, the NIH, and prospective licensing partners. The company is headquartered in Tucson, Arizona with a satellite office in Jupiter, Florida near the Herbert Wertheim UF Scripps Institute, and is led by Founder/CEO Dr. Joe G.N. "Skip" Garcia alongside a small leadership team including a President, fractional CFO, CMO, and CMC lead.

Short descriptiontext

Aqualung Therapeutics is a clinical-stage biotech developing ALT-100 mAb, a humanized monoclonal antibody neutralizing eNAMPT to treat acute respiratory distress syndrome, progressive pulmonary fibrosis, and other inflammatory and fibrotic diseases.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersTucson, United States
HQ citystring
Tucson
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
anti-inflammatory monoclonal antibodies, inflammatory disease therapeutics, pulmonary fibrosis treatment, biopharmaceutical drug development, eNAMPT pathway therapeutics
Industry4 codes
1Monoclonal Antibody Therapeutics (mAbs)
CodeHLAAAAAAPrimaryYes
2Rare Immunology, Autoimmune & Autoinflammatory Therapies
CodeHLAIAIAEPrimaryNo
3Therapeutic Peptides & Protein/Peptide Biologics
CodeHLAAAAAHPrimaryNo
4Fusion Proteins & Fc-Engineered Biologics
CodeHLAAAAADPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Misc Health & Allied Services, Nec8090
Product category
Biopharmaceutical Therapeutics
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Biopharmaceutical Development and Commercialization
TypeOne Time License
Description

Pre-commercial stage biotech company developing novel monoclonal antibody therapeutics. Revenue will be generated through product sales following FDA approval. The company is pursuing development of ALT-100 mAb for multiple inflammatory and fibrotic disease indications.

aqualungtherapeutics.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 6 records shown
1eNamptor
Description

The company's technology platform consisting of ALT-100 mAb (humanized monoclonal antibody), NTyP-100 (nanocarrier), and SELP-100 (fusion immunoglobulin protein), along with biomarker and genotyping tools for targeted clinical development.

aqualungtherapeutics.com
+5 more records
Core offering1 text field

Aqualung Therapeutics is a clinical-stage biopharmaceutical company developing novel monoclonal antibody and biologic therapeutics targeting extracellular NAMPT (eNAMPT) to treat uncontrolled inflammation and fibrosis. Its lead candidate, ALT-100 mAb, is in Phase 2a clinical trials for Acute Respiratory Distress Syndrome (ARDS) and progressive pulmonary fibrosis, supported by a complementary platform that includes the NTyP-100 nanocarrier and SELP-100 fusion immunoglobulin protein.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Phase 1A studies in healthy volunteers reported no serious adverse events
+3 more records
Product overview1 text field

Aqualung Therapeutics is a clinical-stage immunotherapeutics company developing a platform of novel biologics targeting inflammatory and fibrotic diseases. The company's core portfolio consists of three main therapeutic candidates: ALT-100 mAb (a humanized monoclonal antibody neutralizing eNAMPT), NTyP-100 nanocarrier, and SELP-100 fusion immunoglobulin protein. These candidates target the eNAMPT/TLR4 inflammatory pathway to address conditions including Acute Respiratory Distress Syndrome (ARDS), progressive pulmonary fibrosis, radiation-induced lung injury, chorioamnionitis, inflammatory bowel disease, pulmonary hypertension, and prostate cancer.

Product and service3 records
1ALT-100 mAb
CategoryBiologic therapeutic (monoclonal antibody)
Description

Humanized monoclonal antibody (mAb) designed to neutralize extracellular NAMPT (eNAMPT) and disrupt TLR4-mediated inflammatory signaling. Lead therapeutic candidate in Phase 2a clinical trials for Acute Respiratory Distress Syndrome (ARDS) and progressive pulmonary fibrosis, with planned indications across multiple inflammatory and fibrotic diseases.

2NTyP-100 Nanocarrier
CategoryDrug delivery platform technology
Description

Novel nanocarrier technology platform designed for targeted drug delivery in inflammatory and fibrotic disease applications.

3SELP-100 Fusion Immunoglobulin Protein
CategoryBiologic therapeutic (fusion protein)
Description

Fusion immunoglobulin protein platform technology for treating inflammatory conditions, targeting SELPLG/P-selectin glycoprotein ligand 1 in preclinical ARDS studies.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Strong academic partnership including collaboration on ALT-100 program for IPF, research conducted at Herbert Wertheim UF Scripps Institute for Biomedical Innovation & Technology, company affiliated with UF startups ecosystem, CEO serves as Associate Vice President for Research at UF and Director of Center for Inflammation Science and Systems Medicine

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

FibroGen developed pamrevlumab, a monoclonal antibody targeting connective tissue growth factor (CTGF) in idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). Direct competitor to ALT-100 mAb in the PPF/PPF clinical development landscape with a similar biologic-modality approach.

TypeDirect peer
Description

Pliant Therapeutics is developing bexotegrast (an integrin-targeting biologic) for IPF and PPF, in Phase 2b/3 development. Direct clinical-stage peer in pulmonary fibrosis with comparable development-stage dynamics and patient population overlap.

TypeBroad incumbent
Description

United Therapeutics markets Tyvaso (inhaled treprostinil) for pulmonary hypertension and IPF, and is developing broader inflammatory/fibrotic pipelines. As an established commercial player in pulmonary medicine, they represent both a competitor and a potential large-pharma acquirer/partner for Aqualung's lead program.

TypeBroad incumbent
Description

Boehringer Ingelheim markets Ofev (nintedanib), one of two approved therapies for IPF and PPF. As a broad incumbent in pulmonary and inflammatory disease with deep commercial infrastructure, they are the dominant benchmark for any IPF/PPF entrant and a likely strategic acquirer.

TypeDirect peer
Description

Blade Therapeutics (now part of certain hedge fund structures) is developing novel antifibrotic therapies for IPF and other fibrotic diseases. Direct peer in clinical-stage pulmonary fibrosis drug development with comparable mechanism exploration around inflammation-driven fibrosis.

TypeDirect peer
Description

AnaptysBio is a clinical-stage antibody developer advancing wholly-owned mAbs targeting inflammatory and autoimmune pathways (e.g., IL-36R, PD-1 agonist). Comparable as a small-cap inflammation-focused antibody platform with a multi-indication strategy and similar partnership/licensing economics.

TypeDirect peer
Description

Humanigen previously advanced lenzilumab, a GM-CSF-targeting monoclonal antibody, for ARDS and COVID-related acute inflammation. Direct ARDS-focused mAb competitor whose clinical experience provides the regulatory and endpoint benchmark for Aqualung's PUERTA trial.

TypeEmerging player
Description

Galapagos has been developing novel mechanism therapies in IPF (e.g., ziritaxestat, discontinued) and inflammatory bowel disease. Comparable as a mid-cap biotech with parallel inflammation/fibrosis pipeline ambitions, though with a broader small-molecule focus.

TypeBroad incumbent
Description

Genentech/Roche markets Actemra (tocilizumab), used in cytokine storm and ARDS-adjacent indications, and is active across autoimmune/inflammatory biologics. As a broad incumbent, they represent a likely large-pharma partner or acquirer for ALT-100 given their IL-6 pathway experience in critical care.

TypeDirect peer
Description

Athersys developed MultiStem (multipotent adult progenitor cells) for ARDS, advancing through Phase 2/3 trials. Direct ARDS clinical-stage peer in acute inflammatory lung injury with comparable regulatory pathway challenges and trial design considerations.

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 risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment9 records

Each record includes

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

Ideal customer profile2 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
Profiles6 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds6 records

Each record includes

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

Investors4 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&A

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 →

Aqualung Therapeutics

Biopharmaceutical Therapeuticsaqualungtherapeutics.com

Aqualung Therapeutics is a clinical-stage biotech developing ALT-100 mAb, a humanized monoclonal antibody neutralizing eNAMPT to treat acute respiratory distress syndrome, progressive pulmonary fibrosis, and other inflammatory and fibrotic diseases.

What Aqualung Therapeutics does

Aqualung Therapeutics Corporation is a clinical-stage immunotherapeutics company developing a platform of biologic therapies that target extracellular nicotinamide phosphoribosyltransferase (eNAMPT) and its downstream TLR4-mediated inflammatory signaling cascade. The company's lead asset, ALT-100 mAb, is a humanized monoclonal antibody designed to neutralize eNAMPT as an upstream master regulatory cytokine rather than downstream single cytokines, with the goal of interrupting unchecked inflammation and vascular leakage at their source. The pipeline also includes NTyP-100 (a novel nanocarrier delivery platform) and SELP-100 (a fusion immunoglobulin protein targeting SELPLG/P-selectin), together marketed as the eNamptor platform. Lead clinical programs are the PUERTA Phase 2a trial in acute respiratory distress syndrome (ARDS) and the PAISANO Phase 2a trial in progressive pulmonary fibrosis, with additional preclinical-stage exploration across radiation-induced lung injury, NASH, pulmonary hypertension, IBD, lupus vasculitis, prostate cancer, and chorioamnionitis-related preterm birth.

The company is pre-revenue and operates a biotech development model in which operating capital is sourced from a combination of NIH grant awards (STTR and other mechanisms) and venture financing. As of the most recent disclosures, total venture funding includes a $2.5 million convertible note round completed in January 2022, alongside multiple NIH awards. Pricing is not publicly disclosed because no product is commercialized; future revenue is expected to derive from biopharmaceutical product sales following FDA approval and from pharmaceutical licensing or partnership arrangements for global commercialization. The customer base consists of multiple end-market segments — critical care/ICU, pulmonology, radiation oncology, hepatology, rheumatology, gastroenterology, oncology, and obstetrics — but the company's effective near-term "customers" are academic collaborators, the NIH, and prospective licensing partners. The company is headquartered in Tucson, Arizona with a satellite office in Jupiter, Florida near the Herbert Wertheim UF Scripps Institute, and is led by Founder/CEO Dr. Joe G.N. "Skip" Garcia alongside a small leadership team including a President, fractional CFO, CMO, and CMC lead.

Aqualung Therapeutics firmographics

Firmographics
Name
Aqualung Therapeutics
Legal name
Aqualung Therapeutics Corporation
Website
https://aqualungtherapeutics.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
Aqualung Therapeutics is a clinical-stage biotech developing ALT-100 mAb, a humanized monoclonal antibody neutralizing eNAMPT to treat acute respiratory distress syndrome, progressive pulmonary fibrosis, and other inflammatory and fibrotic diseases.
Ownership category
akta.pro rank

Aqualung Therapeutics industry classification

Industry
Product category
Biopharmaceutical Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Services-Misc Health & Allied Services, Nec (8090)
akta.pro primary industry
Monoclonal Antibody Therapeutics (mAbs) (HLAAAAAA)
akta.pro secondary industries
Rare Immunology, Autoimmune & Autoinflammatory Therapies (HLAIAIAE), Therapeutic Peptides & Protein/Peptide Biologics (HLAAAAAH), Fusion Proteins & Fc-Engineered Biologics (HLAAAAAD)

Keywords

  • Anti-inflammatory monoclonal antibodies
  • Inflammatory disease therapeutics
  • Pulmonary fibrosis treatment
  • Biopharmaceutical drug development
  • ENAMPT pathway therapeutics

Where Aqualung Therapeutics is headquartered

Location

Headquarters

HQ city
Tucson
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Aqualung Therapeutics business model

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

Revenue model

  1. Biopharmaceutical Development and Commercialization: Pre-commercial stage biotech company developing novel monoclonal antibody therapeutics. Revenue will be generated through product sales following FDA approval. The company is pursuing development of ALT-100 mAb for multiple inflammatory and fibrotic disease indications.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Aqualung Therapeutics product offering

Product offering

Core offering

Aqualung Therapeutics is a clinical-stage biopharmaceutical company developing novel monoclonal antibody and biologic therapeutics targeting extracellular NAMPT (eNAMPT) to treat uncontrolled inflammation and fibrosis. Its lead candidate, ALT-100 mAb, is in Phase 2a clinical trials for Acute Respiratory Distress Syndrome (ARDS) and progressive pulmonary fibrosis, supported by a complementary platform that includes the NTyP-100 nanocarrier and SELP-100 fusion immunoglobulin protein.

Product overview

Aqualung Therapeutics is a clinical-stage immunotherapeutics company developing a platform of novel biologics targeting inflammatory and fibrotic diseases. The company's core portfolio consists of three main therapeutic candidates: ALT-100 mAb (a humanized monoclonal antibody neutralizing eNAMPT), NTyP-100 nanocarrier, and SELP-100 fusion immunoglobulin protein. These candidates target the eNAMPT/TLR4 inflammatory pathway to address conditions including Acute Respiratory Distress Syndrome (ARDS), progressive pulmonary fibrosis, radiation-induced lung injury, chorioamnionitis, inflammatory bowel disease, pulmonary hypertension, and prostate cancer.

Differentiator

Problem solved

Functional benefit

Brands

  • eNamptor: The company's technology platform consisting of ALT-100 mAb (humanized monoclonal antibody), NTyP-100 (nanocarrier), and SELP-100 (fusion immunoglobulin protein), along with biomarker and genotyping tools for targeted clinical development.
  • ALT-100 mAb
  • NTyP-100
  • SELP-100
  • PAISANO Trial
  • PUERTA Trial

Products and services

  • ALT-100 mAb Humanized monoclonal antibody (mAb) designed to neutralize extracellular NAMPT (eNAMPT) and disrupt TLR4-mediated inflammatory signaling. Lead therapeutic candidate in Phase 2a clinical trials for Acute Respiratory Distress Syndrome (ARDS) and progressive pulmonary fibrosis, with planned indications across multiple inflammatory and fibrotic diseases.
  • NTyP-100 Nanocarrier Novel nanocarrier technology platform designed for targeted drug delivery in inflammatory and fibrotic disease applications.
  • SELP-100 Fusion Immunoglobulin Protein Fusion immunoglobulin protein platform technology for treating inflammatory conditions, targeting SELPLG/P-selectin glycoprotein ligand 1 in preclinical ARDS studies.

Quantifiable outcome

  • Phase 1A studies in healthy volunteers reported no serious adverse events
  • +3 more outcomes

Companies that use Aqualung Therapeutics

Customer profile

Segments9 records

Ideal customer profiles2 records

Aqualung Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Aqualung Therapeutics partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • University of FloridacoreStrategic or Co-development PartnerStrong academic partnership including collaboration on ALT-100 program for IPF, research conducted at Herbert Wertheim UF Scripps Institute for Biomedical Innovation & Technology, company affiliated with UF startups ecosystem, CEO serves as Associate Vice President for Research at UF and Director of Center for Inflammation Science and Systems Medicine

Scale indicators4 records

Recent moves6 records

Expansion highlights5 records

Aqualung Therapeutics competitors and assessment

Company assessment

Direct peers

  • FibroGen: FibroGen developed pamrevlumab, a monoclonal antibody targeting connective tissue growth factor (CTGF) in idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). Direct competitor to ALT-100 mAb in the PPF/PPF clinical development landscape with a similar biologic-modality approach.
  • Pliant Therapeutics: Pliant Therapeutics is developing bexotegrast (an integrin-targeting biologic) for IPF and PPF, in Phase 2b/3 development. Direct clinical-stage peer in pulmonary fibrosis with comparable development-stage dynamics and patient population overlap.
  • Blade Therapeutics: Blade Therapeutics (now part of certain hedge fund structures) is developing novel antifibrotic therapies for IPF and other fibrotic diseases. Direct peer in clinical-stage pulmonary fibrosis drug development with comparable mechanism exploration around inflammation-driven fibrosis.
  • AnaptysBio: AnaptysBio is a clinical-stage antibody developer advancing wholly-owned mAbs targeting inflammatory and autoimmune pathways (e.g., IL-36R, PD-1 agonist). Comparable as a small-cap inflammation-focused antibody platform with a multi-indication strategy and similar partnership/licensing economics.
  • Humanigen (now Kelun-Biotech / lenzilumab successor): Humanigen previously advanced lenzilumab, a GM-CSF-targeting monoclonal antibody, for ARDS and COVID-related acute inflammation. Direct ARDS-focused mAb competitor whose clinical experience provides the regulatory and endpoint benchmark for Aqualung's PUERTA trial.
  • Athersys: Athersys developed MultiStem (multipotent adult progenitor cells) for ARDS, advancing through Phase 2/3 trials. Direct ARDS clinical-stage peer in acute inflammatory lung injury with comparable regulatory pathway challenges and trial design considerations.

Broad incumbents

  • United Therapeutics: United Therapeutics markets Tyvaso (inhaled treprostinil) for pulmonary hypertension and IPF, and is developing broader inflammatory/fibrotic pipelines. As an established commercial player in pulmonary medicine, they represent both a competitor and a potential large-pharma acquirer/partner for Aqualung's lead program.
  • Boehringer Ingelheim: Boehringer Ingelheim markets Ofev (nintedanib), one of two approved therapies for IPF and PPF. As a broad incumbent in pulmonary and inflammatory disease with deep commercial infrastructure, they are the dominant benchmark for any IPF/PPF entrant and a likely strategic acquirer.
  • Genentech (Roche): Genentech/Roche markets Actemra (tocilizumab), used in cytokine storm and ARDS-adjacent indications, and is active across autoimmune/inflammatory biologics. As a broad incumbent, they represent a likely large-pharma partner or acquirer for ALT-100 given their IL-6 pathway experience in critical care.

Emerging players

  • Galapagos NV: Galapagos has been developing novel mechanism therapies in IPF (e.g., ziritaxestat, discontinued) and inflammatory bowel disease. Comparable as a mid-cap biotech with parallel inflammation/fibrosis pipeline ambitions, though with a broader small-molecule focus.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks5 records

Key highlights7 records

Customer concentration

Aqualung Therapeutics social profiles

Digital presence

Aqualung Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Aqualung Therapeutics leadership team

Management profile

Number of profiles

Profiles6 records

Aqualung Therapeutics funding detail

Funding detail

Funding overview

Funding rounds6 records

Investors4 records

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

Aqualung Therapeutics M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Aqualung Therapeutics

What does Aqualung Therapeutics do?

Aqualung Therapeutics is a clinical-stage biopharmaceutical company developing novel monoclonal antibody and biologic therapeutics targeting extracellular NAMPT (eNAMPT) to treat uncontrolled inflammation and fibrosis. Its lead candidate, ALT-100 mAb, is in Phase 2a clinical trials for Acute Respiratory Distress Syndrome (ARDS) and progressive pulmonary fibrosis, supported by a complementary platform that includes the NTyP-100 nanocarrier and SELP-100 fusion immunoglobulin protein.

Is Aqualung Therapeutics a public or private company?

Aqualung Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Aqualung Therapeutics founded?

Aqualung Therapeutics was founded in 2019. It employs 1 to 10 people.

Where is Aqualung Therapeutics based?

Aqualung Therapeutics is headquartered in Tucson, United States, in the North America region.

How does Aqualung Therapeutics make money?

One revenue line is on record: biopharmaceutical Development and Commercialization.

Who are Aqualung Therapeutics's main competitors?

Direct peers on record are FibroGen, Pliant Therapeutics, Blade Therapeutics, AnaptysBio, Humanigen (now Kelun-Biotech / lenzilumab successor) and Athersys. Broad incumbents are United Therapeutics, Boehringer Ingelheim and Genentech (Roche). Galapagos NV is listed as an emerging player.

Does Aqualung Therapeutics have an API?

No public API is recorded for Aqualung Therapeutics.

What industry is Aqualung Therapeutics in?

Aqualung Therapeutics's product category is Biopharmaceutical Therapeutics. Its primary akta.pro industry code is HLAAAAAA, Monoclonal Antibody Therapeutics (mAbs), with a secondary code of HLAIAIAE, Rare Immunology, Autoimmune & Autoinflammatory Therapies. Its NAICS code is 541714 and its SIC code is 8090.

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Live signals
EIN PresswirePhase 2a Study Clinically Validates the eNAMPT Pathway and Demonstrates Favorable Safety Profile of ALT-100 in ARDSAqualung Therapeutics published positive results from its Phase 2a PUERTA trial of ALT-100 in ARDS, showing improved SOFA scores, more ventilator-free days, and reduced inflammatory biomarkers versus placebo. The study also reported a favorable safety profile with adverse events comparable to placebo. The company is now evaluating the optimal clinical development strategy for ALT-100 across inflammatory and fibrotic indications.PR NewswireAqualung Therapeutics Receives FDA Clearance for Phase 2a Lung Fibrosis StudyAqualung Therapeutics received FDA clearance for a Phase 2a study of ALT-100 mAb to treat Progressive Pulmonary Fibrosis. The company plans to initiate the multicenter PAISANO trial upon securing the next round of funding.YahooAqualung Therapeutics Corp., an Immunotherapeutics Biotech Company, Closes a $2.5M Convertible Note Raise With a Committed Series A Lead InvestorAqualung Therapeutics closed a $2.5 million convertible note raise, led by a $1.5 million investment from JSR Life Sciences, bringing its total funding to over $17 million. The capital will facilitate an upcoming 'First in Human' phase 1A safety trial for the ALT-100 mAb therapy and support an IND filing with the US FDA for Acute Respiratory Distress Syndrome (ARDS).PR NewswireAqualung Therapeutics Corporation To Present New Data At Biotech Showcase Investor ConferenceAqualung Therapeutics Corporation will present new data on its lead drug eNamptor™ at the Biotech Showcase investor conference in San Francisco on January 14, 2020. The company has received a $1.7M NIH STTR grant and has a $3M Department of Defense award pending to fund development of treatments for ARDS, a condition affecting approximately 488,000 US patients annually with over 30% mortality and no FDA-approved drugs. The anticipated US market for ARDS treatment is $2.8 billion, and the company expects to complete IND-enabling studies by late 2020 or early 2021.PR NewswireAqualung Therapeutics Corporation Receives $225 Thousand Dollar National Institute of Health (NIH) Grant to Establish Biomarker Panel for Patients with Acute Respiratory Distress SyndromeAqualung Therapeutics Corporation received a $225,000 grant from the National Institutes of Health (NIH) to develop a biomarker panel for patients with Acute Respiratory Distress Syndrome. This funding supports the creation of the CRIT-ICU Panel, which aims to stratify patients into high and low mortality sub-groups to accelerate clinical trial strategies. The initiative seeks to establish a point-of-care test that predicts ICU mortality and identifies responders to emerging therapies like eNamptorTM.PR NewswireAqualung Therapeutics Corporation Receives A $1.7 Million National Institute Of Health (NIH) Fastrack Award To Develop An Novel Immune-Based Therapeutic Antibody For Critically Ill Patients With AcuteAqualung Therapeutics Corporation has received a $1.7 million NIH FASTRACK Award (R42HL145930) to advance eNamptor™, a humanized monoclonal antibody targeting extracellular eNAMPT for treating Acute Respiratory Distress Syndrome. The STTR award will fund lead candidate selection, preclinical studies, pharmacokinetic/pharmacodynamic and toxicology studies in animal models, and submission of an FDA IND application over a three-year period. ARDS has a 30-40% mortality rate with no FDA-approved treatments, making this non-dilutive funding a significant milestone for advancing the therapy toward clinical development.