Evidence map›Paper›PMID 36112543›Full record

ReviewUnited European gastroenterology journal2022

Landscape of new drugs and targets in inflammatory bowel disease.

Sophie Vieujean, Ferdinando D'Amico, Patrick Netter, Silvio Danese, Laurent Peyrin-Biroulet

Open access · hybridAbstract readReview
In one paragraph

Review in United European gastroenterology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Landscape of new drugs and targets in inflammatory bowel disease.United European gastroenterology journal · 2022
    Review
  13. Changing paradigms in management of inflammatory bowel disease.United European gastroenterology journal · 2022
    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

5 authors at 5 institutions in 3 countries.

Sophie VieujeanHepato-Gastroenterology and Digestive Oncology, University Hospital CHU of Liège, Liège, Belgium.ORCID 0000-0002-1859-7146
Ferdinando D'AmicoDepartment of Gastroenterology and Endoscopy, IRCCS San Raffaele Hospital and Vita-Salute San Raffaele University, Milan, Italy.ORCID 0000-0002-8591-6995
Patrick NetterUniversité de Lorraine, CNRS, Laboratoire IMoPA, Nancy, France.
Silvio DaneseDepartment of Gastroenterology and Endoscopy, IRCCS San Raffaele Hospital and Vita-Salute San Raffaele University, Milan, Italy.
Laurent Peyrin-BirouletDepartment of Gastroenterology, University of Lorraine, CHRU-Nancy, Nancy, France.ORCID 0000-0003-2536-6618
Centre Hospitalier Universitaire de Liège · BECentre National de la Recherche Scientifique · FRHumanitas University · ITInserm · FRVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the therapeutic armamentarium of Inflammatory bowel diseases (IBD) physicians has expanded rapidly in recent years, a proportion of patients remain with a suboptimal response to medical treatment due to primary no response, loss of response or intolerance to currently available drugs. Our growing knowledges of IBD pathophysiology has led to the development of a multitude of new therapies over time, which may, 1 day, be able to address this unmet medical need. This review aims to provide physicians an update of emerging therapies in IBD by focusing on drugs currently in phase 3 clinical trials. Among the most promising molecules are anti-IL-23, JAK-inhibitors, anti-integrins and S1P modulators. While the results in terms of efficacy and safety are fairly clear for some classes, the question of safety remains more uncertain for other classes. Molecules at a more preliminary stage of development (phase 1 and 2), one of which may 1 day offer an optimal benefit-risk ratio, will also be presented as well as their respective mechanisms of action.

Indexed as

Inflammatory Bowel DiseasesJanus Kinase InhibitorsClinical Trials, Phase III as TopicHumansJanus Kinase Inhibitorsclinical trialsinflammatory bowel diseasenew drugsphase 1phase 2phase 3

Identifiers

PMID36112543
PMCPMC9752289
OpenAlexW4296028018

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.