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Disease

Lung Diseases, Interstitial

Late-stage therapeutic developmentEmerging researchRising momentum
11
Publications
13
Clinical trials
4
Related conditions
3
Related treatments
4
Related proteins
2024
Latest publication
Current focus
Immunoconjugates biologyTherapeutic developmentTrastuzumab biologyInflammation & immunity
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this disease.

Efficacy and Safety of Trastuzumab Deruxtecan in Patients With HER2-Expressing Solid Tumors: Primary Results From the DESTINY-PanTumor02 Phase II Trial.

Research2023-10-23Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer.

Research2022-03-01The New England journal of medicine

Trastuzumab Deruxtecan in <i>HER2</i>-Mutant Non-Small-Cell Lung Cancer.

Research2021-09-18The New England journal of medicine

Rheumatoid arthritis-interstitial lung disease: manifestations and current concepts in pathogenesis and management.

Research2021-06-23European respiratory review : an official journal of the European Respiratory Society

Trastuzumab Deruxtecan in Previously Treated HER2-Positive Gastric Cancer.

Research2020-05-29The New England journal of medicine

Trastuzumab Deruxtecan in Previously Treated HER2-Positive Breast Cancer.

Research2019-12-11The New England journal of medicine

FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer.

Research2018-12-01The New England journal of medicine

What's happening now

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

Major developments
Upcoming trial readoutHigh impact
Results expected Q4 20272026-07-27
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 Milestones5View
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 timeline6

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)

Clinical trials

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

The current development programme across all trial phases.

Clinical programme
13
All trials
4
Active
8
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).&nbsp;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).&nbsp;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.&nbsp;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).&nbsp;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 ↗

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

11 papers

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

Publications over time
20182024
Most influential

FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer.

The New England journal of medicine · 2018 · 2,091 cites

Trastuzumab Deruxtecan in Previously Treated HER2-Positive Breast Cancer.

The New England journal of medicine · 2020 · 1,483 cites

Trastuzumab Deruxtecan in Previously Treated HER2-Positive Gastric Cancer.

The New England journal of medicine · 2020 · 983 cites

Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer.

The New England journal of medicine · 2022 · 893 cites

Trastuzumab Deruxtecan in <i>HER2</i>-Mutant Non-Small-Cell Lung Cancer.

The New England journal of medicine · 2022 · 751 cites

Efficacy and Safety of Trastuzumab Deruxtecan in Patients With HER2-Expressing Solid Tumors: Primary Results From the DESTINY-PanTumor02 Phase II Trial.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024 · 717 cites
Recent publications
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

4 matches

Key proteins & gene products studied in this disease. Number shows shared papers.

Related conditions

4 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

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.

Causes

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.

Pathophysiology

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.

Risk factors

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.

Current standard of care

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.

Defined in MeSH

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.

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.