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Disease

Lung Diseases

Late-stage therapeutic developmentEmerging researchRising momentum
16
Publications
20
Clinical trials
7
Related conditions
2025
Latest publication
Latest activity
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Recent clinical, regulatory, research and industry developments relating to this disease.

Application of metagenomic next-generation sequencing in pathogen detection of lung infections.

Research2025-05-01Frontiers in cellular and infection microbiology

Inflammation unites diverse acute and chronic diseases.

Research2024-07-24European journal of clinical investigation

The Association between Dyslipidemia and Pulmonary Diseases.

Research2024-07-12Journal of atherosclerosis and thrombosis

Update of EULAR recommendations for the treatment of systemic sclerosis.

Research2016-11-09Annals of the rheumatic diseases

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Major developments
Important regulatory approvalImportant
Nintedanib Viatris is indicated in adults for the treatment of idiopathic pulmonary fibrosis (IPF). Nintedanib Viatris is also indicated in adults for the treatment of other chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype. Nintedanib Viatris is indicated in children and adolescents from 6 to 17 years old for the treatment of clinically significant, progressive fibrosing interstitial lung diseases (ILDs). Nintedanib Viatris is indicated in adults, adolescents and children aged 6 years and older for the treatment of systemic sclerosis associated interstitial lung disease (SSc-ILD).2025-08-22
Clinical Milestones8View
Regulatory Updates1View
  • 2025-08-22Approval — NintedanibNintedanib Viatris is indicated in adults for the treatment of idiopathic pulmonary fibrosis (IPF). Nintedanib Viatris is also indicated in adults for the treatment of other chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype. Nintedanib Viatris is indicated in children and adolescents from 6 to 17 years old for the treatment of clinically significant, progressive fibrosing interstitial lung diseases (ILDs). Nintedanib Viatris is indicated in adults, adolescents and children aged 6 years and older for the treatment of systemic sclerosis associated interstitial lung disease (SSc-ILD).
Activity timeline9

Therapeutic landscape

Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.

Approved & established therapies
Nintedanibapproved

Approval — Nintedanib Viatris is indicated in adults for the treatment of idiopathic pulmonary fibro… (2025)

Azathioprineapproved

Approval — Jayempi is indicated in combination with other immunosuppressive agents for the prophylax… (2021)

Clinical trials

14 sponsors · 2 new · 1 completed in the last 12 months (net +1)

The current development programme across all trial phases.

Clinical programme
20
All trials
6
Active
11
Late-stage
6
Completed
Late-stage studies
Recruiting
Recently completed

Regulatory timeline

Drug regulatory events matched to this condition by indication — EMA.

First approvals
2025emaApprovalNintedanib· Nintedanib Viatris is indicated in adults for the treatment of idiopathic pulmonary fibrosis (IPF). Nintedanib Viatris is also indicated in adults for the treatment of other chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype. Nintedanib Viatris is indicated in children and adolescents from 6 to 17 years old for the treatment of clinically significant, progressive fibrosing interstitial lung diseases (ILDs). Nintedanib Viatris is indicated in adults, adolescents and children aged 6 years and older for the treatment of systemic sclerosis associated interstitial lung disease (SSc-ILD). source ↗
2024emaApprovalNintedanib· Nintedanib Accord is indicated in adults for the treatment of idiopathic pulmonary fibrosis (IPF). Nintedanib Accord is also indicated in adults for the treatment of other chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype (see section 5.1). Nintedanib Accord is indicated in adults for the treatment of systemic sclerosis associated interstitial lung disease (SSc-ILD). Nintedanib Accord is indicated in adults for the treatment of idiopathic pulmonary fibrosis (IPF). Nintedanib Accord is also indicated in adults for the treatment of other chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype. Nintedanib Accord is indicated in children and adolescents from 6 to 17 years old for the treatment of clinically significant, progressive fibrosing interstitial lung diseases (ILDs). Nintedanib Accord is indicated in adults, adolescents and children aged 6 years and older for the treatment of systemic sclerosis associated interstitial lung disease (SSc-ILD). source ↗
2021emaApprovalAzathioprine· Jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. Azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). Jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. Jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases: severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – DMARDs) auto-immune hepatitis  systemic lupus erythematosus dermatomyositis polyarteritis nodosa pemphigus vulgaris and bullous pemphigoid Behçet’s disease refractory auto-immune haemolytic anaemia, caused by warm IgG antibodies chronic refractory idiopathic thrombocytopenic purpura Jayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (IBD) (Crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. It is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3 Jayempi is indicated for the treatment of generalised myasthenia gravis. Depending on the severity of the disease, Jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment. source ↗

European Medicines Agency (CC BY 4.0). Events are matched to this condition by drug indication text — approvals/updates for drugs indicated for it, not disease-specific acts.

Research activity

16 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Publications over time
19972025
Most influential
Recent publications
Major themes8
  • Lung Diseases4
  • Anti-Bacterial Agents1
  • Bacteria1
  • Blockchain1
  • Cardiovascular Diseases1
  • Cellular Senescence1
  • Confidentiality1
  • COVID-191
Leading journals6
  • Allergy1
  • Annals of the rheumatic diseases1
  • Annual review of physiology1
  • Clinical microbiology reviews1
  • European journal of clinical investigation1
  • Frontiers in cellular and infection microbiology1
Leading researchers8
  • Becker M2
  • Adcock IM1
  • Adler A1
  • Allanore Y1
  • Altmüller J1
  • Amato MB1
  • Aschenbrenner AC1
  • Augustin M1
Affiliations (unnormalised)6
  • Ghent University Hospital2
  • Ambroise Paré Hospital1
  • Asthma and COPD Competence Center1
  • Basel University1
  • Brigham and Women's Hospital1
  • Carleton University1

Related conditions

7 matches

Diseases frequently studied alongside this one. Number shows shared papers.

Disease profile

A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.

Overview

Lung diseases are pathological processes involving any part of the lung. The literature grounding here treats them as a broad category that includes acute and chronic conditions, with attention to diagnosis, microbiology, etiology, immunology, and drug therapy. Aging-related changes in the lung are also discussed as part of this disease space.

Causes

The supplied grounding does not support a single cause for lung diseases because it is a broad category rather than one disorder. The literature indicates that etiology varies by condition and may include infectious causes, immune-mediated processes, and age-associated biological changes. Postacute sequelae after SARS-CoV-2 infection are also covered as one disease-related context.

Pathophysiology

The grounding supports several mechanisms relevant to lung disease, including aging and cellular senescence. Aging of the lung is associated with molecular and physiological changes that alter lung function, reduce pulmonary remodeling and regenerative capacity, and increase susceptibility to acute and chronic disease. The literature also points to altered interactions between pulmonary resident cells and systemic immune cells, as well as immune dysregulation in some lung-related conditions.

Risk factors

Older age is supported as a risk factor because natural lung aging is associated with increased susceptibility to infection and chronic lung disease. The grounding also indicates that risk varies by disease subtype and may depend on factors such as infection-related exposures and immune status. No broader unified risk profile is supported for all lung diseases.

Current standard of care

The supplied grounding does not support a single standard of care for all lung diseases because treatment depends on the specific underlying condition. The literature only supports that drug therapy is one of the covered management areas, and that diagnosis and clinical monitoring are important components of care. For chronic lung disease assessment, chest electrical impedance tomography is described as a clinical tool for monitoring regional lung ventilation and pulmonary function.

AI-generated summary grounded in MeSH and 6 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

Pathological processes involving any part of the LUNG.

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.