Evidence map›Paper›PMID 31218221›Full record

ArticleERJ open research2019

Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two

Jennifer L Taylor-Cousar, Marcus A Mall, Bonnie W Ramsey, Edward F McKone, Elizabeth Tullis, Gautham Marigowda, Charlotte M McKee, David Waltz, Samuel M Moskowitz, Jessica Savage and 2 more

Open access · goldAbstract read
In one paragraph

Article in ERJ open research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Clinimetric properties of field exercise tests in cystic fibrosis: a systematic review.European respiratory review : an official journal of the European Respiratory Society · 2024
    Pooled it
  2. Trial
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  6. Review
  7. Article
  8. Article
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  11. Lentiviral Gene Therapy for Cystic Fibrosis: A Promising Approach and First-in-Human Trial.American journal of respiratory and critical care medicine · 2024
    Review
  12. Article
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  15. Review
  16. Article
  17. Article
  18. Observational
  19. Review
  20. Functional restoration of a CFTR splicing mutation through RNA delivery of CRISPR adenine base editor.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    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

12 authors at 7 institutions in 4 countries.

Jennifer L Taylor-CousarNational Jewish Health, Denver, CO, USA.
Marcus A MallCharité - Universitätsmedizin Berlin, Berlin Institute of Health, German Center for Lung Research, Berlin, Germany.
Bonnie W RamseySeattle Children's Hospital, Seattle, WA, USA.
Edward F McKoneSt Vincent's University Hospital and University College Dublin School of Medicine, Dublin, Ireland.
Elizabeth TullisSt Michael's Hospital, Toronto, ON, Canada.
Gautham MarigowdaVertex Pharmaceuticals Inc., Boston, MA, USA.
Charlotte M McKeeVertex Pharmaceuticals Inc., Boston, MA, USA.
David WaltzVertex Pharmaceuticals Inc., Boston, MA, USA.
Samuel M MoskowitzVertex Pharmaceuticals Inc., Boston, MA, USA.
Jessica SavageVertex Pharmaceuticals Inc., Boston, MA, USA.
Fengjuan XuanVertex Pharmaceuticals Inc., Boston, MA, USA.
Steven M RoweGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID https://orcid.org/0000-0001-9045-0133
Vertex Pharmaceuticals (United States) · USGerman Center for Lung Research · DENational Jewish Health · USSeattle Children's Hospital · USSt. Michael's Hospital · CAUniversity College Dublin · IEUniversity of Alabama at Birmingham · US

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Brian R. Davis · 2007 to 2026
$23.0M
Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss · 2010 to 2026
$21.4M
Translational Program in CFTR-Related Airway DiseasesR35HL135816 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2017 to 2022
$6.3M
NHLBI NIH HHS R35 HL135816NIDDK NIH HHS P30 DK072482NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator gene (

Identifiers

PMID31218221
PMCPMC6571452
OpenAlexW2952212183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.