Evidence map›Paper›PMID 41595688›Full record

ReviewBiomedicines2026

Most Promising Emerging Therapies for Pulmonary Fibrosis: Targeting Novel Pathways.

Lorenzo Carriera, Roberto Lipsi, Meridiana Dodaj, Riccardo Inchingolo, Andrea Smargiassi, Angelo Coppola, Pier-Valerio Mari, Roberto Barone, Simone Ielo, Raffaele Scala and 1 more

Abstract readReview
In one paragraph

Review in Biomedicines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
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

11 authors.

Lorenzo CarrieraFacoltà di Medicina e Chirurgia, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.ORCID 0009-0006-2538-1278
Roberto LipsiDepartment of Pulmonology and Sub-Intensive Respiratory Unit, Ospedale Santa Maria della Misericordia, 06156 Perugia, Italy.
Meridiana DodajDepartment of Pulmonology and Sub-Intensive Respiratory Unit, Ospedale Santa Maria della Misericordia, 06156 Perugia, Italy.
Riccardo InchingoloUOC Pneumologia, Dipartimento Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.ORCID 0000-0003-2843-9966
Andrea SmargiassiUOC Pneumologia, Dipartimento Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.ORCID 0000-0003-0637-7282
Angelo CoppolaUOC Pneumologia, Ospedale San Filippo Neri-ASL Roma 1, 00135 Rome, Italy.
Pier-Valerio MariInternal Medicine, San Carlo di Nancy Hospital, 00165 Rome, Italy.ORCID 0000-0002-3307-217X
Roberto BaroneFacoltà di Medicina e Chirurgia, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.ORCID 0009-0003-7257-1080
Simone IeloPulmonology and Respiratory Intensive Care Unit, Ospedale San Donato, USL Toscana Sud-Est, 52100 Arezzo, Italy.ORCID 0009-0002-2838-423X
Raffaele ScalaPulmonology and Respiratory Intensive Care Unit, Ospedale San Donato, USL Toscana Sud-Est, 52100 Arezzo, Italy.
Luca RicheldiUOC Pneumologia, Dipartimento Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial lung diseases (ILDs) encompass a heterogeneous group of disorders characterized by varying degrees of inflammation and fibrosis. Despite advances in understanding the pathogenesis, therapeutic options remain limited, particularly for patients with progressive phenotypes. Current international guidelines for idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF) emphasize the need for antifibrotic strategies and call for novel pharmacological interventions targeting key molecular pathways involved in fibrogenesis. This review provides a comprehensive overview of the most promising emerging pharmacological agents for ILDs, with particular attention to their mechanisms of action, efficacy, and safety profiles as reported in recent preclinical and clinical studies. The recent approval of Nerandomilast and the ongoing phase III trials of other agents mark a pivotal transition toward a new generation of antifibrotic therapies, aiming to achieve more effective disease control and improved patient outcomes. In view of an enlargement of active drugs aiming at controlling the disease with different mechanisms, the Authors underline the need for a "precision medicine" model to be applied to each ILD phenotyped patient, mirroring what already happens for other respiratory diseases.

Indexed as

antifibrotic therapyIPFnerandomilastPPFpulmonary fibrosis

Identifiers

PMID41595688
PMCPMC12839304

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.