Lung Diseases, Interstitial
Recent clinical, regulatory, research and industry developments relating to this disease.
Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer.
Trastuzumab Deruxtecan in <i>HER2</i>-Mutant Non-Small-Cell Lung Cancer.
Trastuzumab Deruxtecan in Previously Treated HER2-Positive Gastric Cancer.
Trastuzumab Deruxtecan in Previously Treated HER2-Positive Breast Cancer.
FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
- 1 regulatory approval from EMA on record.
- 3 clinical trials expected to report results, the earliest in Q2 2027.
- Q2 2027A Phase 1, Study of Nebulized Matrix - Allogeneic Human Amniotic Fluid (HAF) In Patients With Interstitial Lung Disease: AIRMID Trial
- Q4 2027Phase IIa Investigation of H01 in Adults With Interstitial Lung Disease (The SOLIS Study)
- Q4 2028A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Belimumab Administered Subcutaneously in Adults With Interstitial Lung Disease (ILD) Associated With Connective Tissue Disease (CTD)
Clinical MilestonesViewHide
- 2026-03-04An Open-label Trial of the Long-term Safety and Tolerability of Nintedanib Per os, on Top of Standard of Care, Over at Least 3 Years, in Children and Adolescents With Clinically Significant Fibrosing Interstitial Lung Disease (InPedILD®-ON)Results posted
- 2026-01-09A Double Blind, Randomized, Placebo-controlled Trial Evaluating the Efficacy and Safety of BI 1015550 Over at Least 52 Weeks in Patients With Progressive Fibrosing Interstitial Lung Diseases (PF-ILDs)Results posted
- 2026-07-27Phase IIa Investigation of H01 in Adults With Interstitial Lung Disease (The SOLIS Study)Results expected Q4 2027
- 2026-03-03A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Belimumab Administered Subcutaneously in Adults With Interstitial Lung Disease (ILD) Associated With Connective Tissue Disease (CTD)Results expected Q4 2028
- 2026-01-29A Phase 1, Study of Nebulized Matrix - Allogeneic Human Amniotic Fluid (HAF) In Patients With Interstitial Lung Disease: AIRMID TrialResults expected Q2 2027
Regulatory UpdatesViewHide
- 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).
- 2026-07-27ClinicalPhase IIa Investigation of H01 in Adults With Interstitial Lung Disease (The SOLIS Study)Results expected Q4 2027
- 2026-03-04ClinicalAn Open-label Trial of the Long-term Safety and Tolerability of Nintedanib Per os, on Top of Standard of Care, Over at Least 3 Years, in Children and Adolescents With Clinically Significant Fibrosing Interstitial Lung Disease (InPedILD®-ON)Results posted
- 2026-03-03ClinicalA Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Belimumab Administered Subcutaneously in Adults With Interstitial Lung Disease (ILD) Associated With Connective Tissue Disease (CTD)Results expected Q4 2028
- 2026-01-29ClinicalA Phase 1, Study of Nebulized Matrix - Allogeneic Human Amniotic Fluid (HAF) In Patients With Interstitial Lung Disease: AIRMID TrialResults expected Q2 2027
- 2026-01-09ClinicalA Double Blind, Randomized, Placebo-controlled Trial Evaluating the Efficacy and Safety of BI 1015550 Over at Least 52 Weeks in Patients With Progressive Fibrosing Interstitial Lung Diseases (PF-ILDs)Results posted
- 2025-08-22RegulatoryApproval — 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).
Therapeutic landscape
Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.
Approval — Nintedanib Viatris is indicated in adults for the treatment of idiopathic pulmonary fibro… (2025)
Clinical trials
The current development programme across all trial phases.
Regulatory timeline
Drug regulatory events matched to this condition by indication — EMA.
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
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Major themes8
- Lung Diseases, Interstitial5
- Carcinoma, Non-Small-Cell Lung2
- Immunoconjugates2
- Lung Neoplasms2
- Pneumonia2
- Antineoplastic Agents1
- Arthritis, Rheumatoid1
- Breast Neoplasms1
Leading journals6
- The New England journal of medicine5
- Cancer treatment reviews1
- ESMO open1
- European respiratory review : an official journal of the European Respiratory Society1
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology1
- Respiratory research1
Leading researchers8
- Iwata H3
- Andre F2
- Hurvitz SA2
- Im SA2
- Kim SB2
- Lee C2
- Li BT2
- Modi S2
Affiliations (unnormalised)6
- Memorial Sloan Kettering Cancer Center3
- Icahn School of Medicine at Mount Sinai2
- Advanced Cancer Translational Research Institute1
- Aichi Cancer Center Hospital1
- Asan Medical Center1
- Brigham and Women's Hospital and Dana Farber Cancer Institute1
Disease biology
Key proteins & gene products studied in this disease. Number shows shared papers.
Related conditions
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.
Interstitial lung diseases are a diverse group of disorders that affect the lung parenchyma. They are characterized by inflammation that begins in the pulmonary alveoli and extends into the interstitium, which can progress to diffuse pulmonary fibrosis. They are classified by known or unknown etiology and by radiological-pathological features.
The grounding supports both idiopathic and known-cause forms of interstitial lung disease. It specifically includes chemically induced disease, such as drug-related interstitial lung disease/pneumonitis associated with trastuzumab deruxtecan. It also supports interstitial lung disease associated with rheumatoid arthritis as a disease-related cause.
The core process is initial inflammation in the pulmonary alveoli with extension into the interstitium and beyond. This inflammatory injury can lead to diffuse pulmonary fibrosis. In rheumatoid arthritis-associated interstitial lung disease, the literature also emphasizes evolving concepts in pulmonary fibrosis pathogenesis.
The grounding supports rheumatoid arthritis as a condition associated with interstitial lung disease, particularly rheumatoid arthritis-associated ILD. Exposure to trastuzumab deruxtecan is a risk for drug-related interstitial lung disease/pneumonitis. The supplied material does not support additional risk factors.
Management is described at the level of diagnosis and drug therapy rather than specific regimens. For drug-related interstitial lung disease/pneumonitis, the literature emphasizes proactive monitoring, diagnosis of exclusion, and management of the adverse event. For rheumatoid arthritis-associated interstitial lung disease, the review notes therapeutic strategies and a rational clinical approach to diagnosis and management, but the supplied grounding does not support specific treatment classes beyond general management.
AI-generated summary grounded in MeSH and 2 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.
Reference
Authoritative identity, definition & identifiers.
A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.
- 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.