Evidence map›Paper›PMID 29018526›Full record

ArticleBMJ open respiratory research2017

Design of the PF-ILD trial: a double-blind, randomised, placebo-controlled phase III trial of nintedanib in patients with progressive fibrosing interstitial lung disease.

Kevin R Flaherty, Kevin K Brown, Athol U Wells, Emmanuelle Clerisme-Beaty, Harold R Collard, Vincent Cottin, Anand Devaraj, Yoshikazu Inoue, Florence Le Maulf, Luca Richeldi and 4 more

3 registry-linked trialsAbstract read
In one paragraph

Article in BMJ open respiratory research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 94 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 4 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02999178 phase3completednot on this map

A Double Blind, Randomized, Placebo-controlled Trial Evaluating the Efficacy and Safety of Nintedanib Over 52 Weeks in Patients With Progressive Fibrosing Interstitial Lung Disease (PF-ILD)

TypeinterventionalSponsorBoehringer IngelheimRan2017 to 2019Enrolled663ConditionsLung Diseases, InterstitialArmsNintedanib, Placebo
NCT05828953 phase2active not recruitingnot on this mapstarted 2021, after this paper: background citation

A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial of Anlotinib Capsules for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)/Progressive Fibrosis-interstitial Lung Disease (PF-ILDs)

TypeinterventionalSponsorFirst Affiliated Hospital of Wenzhou Medical UniversityRan2021 to 2026Enrolled30ConditionsInterstitial Lung DiseasesArmsAnlotinib, Placebo
NCT06297096 phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Multicentre Clinical Trial Evaluating the Safety and Efficacy of the Combination of Nintedanib+Tocilizumab Compared to Standard Treatment in Patients With Systemic Sclerosis and Interstitial Lung Disease. Analysis With Theranostic Approach

TypeinterventionalSponsorNational Institute of Geriatrics, Rheumatology and Rehabilitation, PolandRan2025 to 2028Enrolled86ConditionsSystemic Sclerosis, Interstitial Lung DiseaseArmsTocilizumab, Nintedanib, Standard therapy
3 · Its place in the literature

Who cites it

94 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Effect of breathing exercises on patients with interstitial lung disease: A systematic review and meta-analysis.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2024
    Pooled it
  3. Guideline
  4. Pooled it
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Article
  10. Article
  11. Progressive pulmonary fibrosis: the importance of identification and intervention.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

34 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Kevin R FlahertyDivision of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Kevin K BrownDepartment of Medicine, National Jewish Health, Denver, Colorado, USA.
Athol U WellsInterstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.
Emmanuelle Clerisme-BeatyBoehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut, USA.
Harold R CollardDepartment of Medicine, University of California, San Francisco, San Francisco, California, USA.
Vincent CottinRespiratory Diseases Department, National Reference Center for Rare Pulmonary Diseases, Respiratory Diseases Department, Louis Pradel Hospital, Claude Bernard Lyon 1 University, Lyon, France.
Anand DevarajDepartment of Radiology, Royal Brompton Hospital, London, UK.
Yoshikazu InoueClinical Research Center, National Hospital Organization, Kinki-Chuo Chest Medical Center, Osaka, Japan.
Florence Le MaulfBoehringer Ingelheim France SAS Reims, Reims, France.
Luca RicheldiUniversità Cattolica del Sacro Cuore, Fondazione Policlinico A. Gemelli, Rome, Italy.
Hendrik SchmidtBoehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.
Simon WalshDepartment of Radiology, King's College Hospital, London, UK.
William MezzanotteBoehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut, USA.
Rozsa Schlenker-HercegBoehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

600 patients aged ≥18 years will be randomised in a 1:1 ratio to nintedanib or placebo. Patients with diagnosis of IPF will be excluded. The study population will be enriched with two-thirds having a usual interstitial pneumonia-like pattern on HRCT. The primary endpoint is the annual rate of decline in forced vital capacity over 52 weeks. The main secondary endpoints are the absolute change from baseline in King's Brief Interstitial Lung Disease Questionnaire total score, time to first acute interstitial lung disease exacerbation or death and time to all-cause mortality over 52 weeks. ETHICS AND DISSEMINATION: The trial is conducted in accordance with the Declaration of Helsinki, the International Conference on Harmonisation Tripartite Guideline for Good Clinical Practice (GCP) and Japanese GCP regulations. TRIAL REGISTRATION NUMBER: NCT02999178.

Indexed as

interstitial fibrosisrare lung diseases

Identifiers

PMID29018526
PMCPMC5604725

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.