Chronic Pulmonary Infections Pipeline: 10+ Leading Companies Driving the Next Wave of Innovative Therapeutics and Precision Treatments | DelveInsight

The chronic pulmonary infections market is undergoing a significant transformation, driven by pioneering companies such as Chiesi Farmaceutici, Armata Pharmaceuticals, Genentech, Altesa Biosciences, and Kinaset Therapeutics. With the advancement of novel inhaled antimicrobials, bacteriophage therapies, targeted immunomodulators, and precision diagnostics, these innovators are reshaping the treatment landscape for persistent lung infections. The current pipeline is focused on addressing antibiotic resistance, enhancing pathogen-specific therapies, and improving outcomes in high-risk populations such as those with COPD and cystic fibrosis. These next-gen approaches offer promising solutions for long-term infection control and improved respiratory health.

DelveInsight's "Chronic Pulmonary Infections Pipeline Insight, 2025" comprehensively analyzes the current clinical landscape and growth prospects in the chronic pulmonary infections market. The report covers disease insights, treatment guidelines, and a detailed pipeline assessment from preclinical to marketed stages. It includes drug mechanisms, clinical studies, regulatory progress, and key developments such as collaborations, mergers, funding, and designations.

For emerging chronic pulmonary infections drugs, the chronic pulmonary infections pipeline analysis report provides a 360° view of the therapeutic landscape by development stage, product type, route of administration, molecule type, and mechanism of action (MOA). The pipeline research covers business opportunities, challenges, future partnerships, strong competitors, and growth strategies.

Key Takeaways from the Chronic Pulmonary Infections Pipeline Report
• DelveInsight's chronic pulmonary infections pipeline analysis depicts a strong space with 10+ active players working to develop 15+ pipeline drugs for chronic pulmonary infections treatment.
• The leading chronic pulmonary infections companies include Chiesi Farmaceutici, Armata Pharmaceuticals, Genentech, Altesa Biosciences, Kinaset Therapeutics, Apogee Therapeutics, and others are evaluating their lead assets to improve the chronic pulmonary infections treatment landscape.
• Key chronic pulmonary infections pipeline therapies in various stages of development include Tanimilast, AP-PA02, Astegolimab, Vapendavir, KN-002, APG808, and others.
• In March 2025, Japan's Ministry of Health, Labour and Welfare granted marketing and manufacturing authorization for Dupixent (dupilumab) to treat chronic obstructive pulmonary disease (COPD) in adults with inadequate control using existing therapies.
• In February 2025, Insmed Incorporated announced that the FDA informed the company it does not plan to hold an advisory committee meeting to discuss the New Drug Application (NDA) for brensocatib for patients with non-cystic fibrosis bronchiectasis.
• In December 2024, Inogen received FDA 510(k) clearance for its SIMEOX 200 Airway Clearance Device, expanding its respiratory product portfolio in the U.S. The upgraded version of the original Simeox uses high-frequency oscillatory vibrations and intermittent negative pressure during exhalation to improve bronchial drainage in patients with chronic lung diseases like Bronchiectasis, COPD, Cystic Fibrosis, and Primary Ciliary Dyskinesia.
• In September 2024, Regeneron Pharmaceuticals, Inc. and Sanofi announced FDA approval of Dupixent® (dupilumab) as an add-on maintenance treatment for adults with inadequately controlled chronic obstructive pulmonary disease (COPD) with an eosinophilic phenotype. Dupixent is the first biologic approved in the U.S. for
• In September 2024, GSK plc announced positive results from the Phase III MATINEE trial of Nucala (mepolizumab) in adults with chronic obstructive pulmonary disease (COPD). The trial demonstrated that adding Nucala to optimized inhaled maintenance therapy significantly reduced the annualized rate of moderate/severe exacerbations compared to placebo in COPD patients with type 2 inflammation.

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Chronic Pulmonary Infections Overview
Chronic pulmonary infections are long-lasting lung infections that progress slowly and often resist treatment, requiring prolonged care. They are commonly caused by bacteria (e.g., Mycobacterium tuberculosis, Pseudomonas aeruginosa), fungi (Aspergillus), and sometimes viruses, especially in people with conditions like COPD, cystic fibrosis, or weakened immunity. Symptoms include persistent cough, blood-tinged sputum, fatigue, breathlessness, chest pain, fever, night sweats, and weight loss. If left untreated, these infections can lead to complications like bronchiectasis or lung abscesses.

Diagnosis involves clinical evaluation, imaging (X-ray or CT), and lab tests such as sputum cultures, bronchoscopy, or PCR. Treatments are pathogen-specific and often lengthy. TB, for instance, requires multi-drug regimens over several months. NTM and Pseudomonas infections may need inhaled or IV antibiotics, while fungal infections are managed with antifungals. In severe or unresponsive cases, surgery may be needed. Effective management also includes treating underlying diseases and maintaining good pulmonary hygiene.

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Chronic Pulmonary Infections Treatment Analysis: Drug Profile
Tanimilast (CHF6001): Chiesi Farmaceutici
Tanimilast is an innovative inhaled phosphodiesterase 4 (PDE4) inhibitor developed by Chiesi Farmaceutici for the treatment of chronic inflammatory lung diseases such as COPD and asthma. By targeting airway inflammation, it helps manage exacerbations commonly seen in chronic pulmonary conditions. Clinical studies have demonstrated its potential in improving lung function and reducing flare-ups in patients with COPD, making it a promising candidate for treating chronic pulmonary infections associated with underlying inflammation. The drug is currently in Phase III development for this indication.

AP-PA02: Armata Pharmaceuticals
AP-PA02 is a cutting-edge phage therapy developed by Armata Pharmaceuticals, specifically designed to combat Pseudomonas aeruginosa-driven respiratory infections. This formulation comprises a potent cocktail of natural bacteriophages, each selected for its broad host range and ability to target different receptor classes on P. aeruginosa. Engineered for synergistic action, AP-PA02 is delivered via inhalation in a sterile liquid form and manufactured under cGMP conditions at Armata's California facility. It is currently in Phase II clinical trials for the treatment of chronic pulmonary infections.

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Chronic Pulmonary Infections Therapeutics Assessment
By Product Type
• Mono
• Combination
• Mono/Combination.

By Stage
• Late-stage products (Phase III)
• Mid-stage products (Phase II)
• Early-stage product (Phase I) along with the details of
• Pre-clinical and Discovery stage candidates
• Discontinued & Inactive candidates

By Route of Administration
• Intravenous
• Subcutaneous
• Oral
• Intramuscular

By Molecule Type
• Monoclonal antibody
• Small molecule
• Peptide

Scope of the Chronic Pulmonary Infections Pipeline Report
• Coverage: Global
• Key Chronic Pulmonary Infections Companies: Chiesi Farmaceutici, Armata Pharmaceuticals, Genentech, Altesa Biosciences, Kinaset Therapeutics, Apogee Therapeutics, and others.
• Key Chronic Pulmonary Infections Pipeline Therapies: Tanimilast, AP-PA02, Astegolimab, Vapendavir, KN-002, APG808, and others.

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Table of Contents
1. Introduction
2. Executive Summary
3. Chronic Pulmonary Infections Pipeline: Overview
4. Analytical Perspective In-depth Commercial Assessment
5. Chronic Pulmonary Infections Pipeline Therapeutics
6. Chronic Pulmonary Infections Pipeline: Late-Stage Products (Phase III)
7. Chronic Pulmonary Infections Pipeline: Mid-Stage Products (Phase II)
8. Chronic Pulmonary Infections Pipeline: Early Stage Products (Phase I)
9. Therapeutic Assessment
10. Inactive Products
11. Company-University Collaborations (Licensing/Partnering) Analysis
12. Key Companies
13. Key Products
14. Unmet Needs
15. Market Drivers and Barriers
16. Future Perspectives and Conclusion
17. Analyst Views
18. Appendix

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This release was published on openPR.