Evidence map›Paper›PMID 29615049›Full record

Trial reportRespiratory research2018

A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial.

Timm Greulich, Jens M Hohlfeld, Petra Neuser, Katrin Lueer, Andreas Klemmer, Carmen Schade-Brittinger, Susanne Harnisch, Holger Garn, Harald Renz, Ursula Homburg and 6 more

Open access · goldAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Respiratory research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Perspectives in Therapy of Chronic Rhinosinusitis.Diagnostics (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Future Trends in Nebulized Therapies for Pulmonary Disease.Journal of personalized medicine · 2020
    Review
  17. 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

16 authors at 6 institutions in 1 country.

Timm GreulichDepartment of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-University, Member of the German Centre for Lung Research (DZL), Marburg, Germany. greulich@med.uni-marburg.de.ORCID 0000-0002-2368-3014
Jens M HohlfeldDepartment of Respiratory Medicine, Hannover Medical School, Fraunhofer Institute for Toxicology and Experimental Medicine, Member of the German Centre for Lung Research (DZL), Hannover, Germany.
Petra NeuserCoordinating Center for Clinical Trials, Member of the German Centre for Lung Research (DZL), Philipps-University, Marburg, Germany.
Katrin LueerDepartment of Respiratory Medicine, Hannover Medical School, Fraunhofer Institute for Toxicology and Experimental Medicine, Member of the German Centre for Lung Research (DZL), Hannover, Germany.
Andreas KlemmerDepartment of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-University, Member of the German Centre for Lung Research (DZL), Marburg, Germany.
Carmen Schade-BrittingerCoordinating Center for Clinical Trials, Member of the German Centre for Lung Research (DZL), Philipps-University, Marburg, Germany.
Susanne HarnischCoordinating Center for Clinical Trials, Member of the German Centre for Lung Research (DZL), Philipps-University, Marburg, Germany.
Holger GarnDepartment of Medicine, Institute of Laboratory Medicine and Pathobiochemistry - Molecular Diagnostics, Member of the German Centre for Lung Research (DZL), Philipps-University, Marburg, Germany.
Harald RenzDepartment of Medicine, Institute of Laboratory Medicine and Pathobiochemistry - Molecular Diagnostics, Member of the German Centre for Lung Research (DZL), Philipps-University, Marburg, Germany.
Ursula HomburgSterna Biologicals GmbH & Co. KG, Marburg, Germany.
Jonas RenzSterna Biologicals GmbH & Co. KG, Marburg, Germany.
Anne KirstenPulmonary Research Institute at LungenClinic Grosshansdorf, Airway Research Center North (ARCN), Member of the German Centre for Lung Research (DZL), Grosshansdorf, Germany.
Frauke PedersenPulmonary Research Institute at LungenClinic Grosshansdorf, Airway Research Center North (ARCN), Member of the German Centre for Lung Research (DZL), Grosshansdorf, Germany.
Meike MüllerDepartment of Respiratory Medicine, Hannover Medical School, Fraunhofer Institute for Toxicology and Experimental Medicine, Member of the German Centre for Lung Research (DZL), Hannover, Germany.
Claus F VogelmeierDepartment of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-University, Member of the German Centre for Lung Research (DZL), Marburg, Germany.
Henrik WatzPulmonary Research Institute at LungenClinic Grosshansdorf, Airway Research Center North (ARCN), Member of the German Centre for Lung Research (DZL), Grosshansdorf, Germany.
German Center for Lung Research · DELungenClinic Grosshansdorf · DEMedizinische Hochschule Hannover · DESterna Biologicals (Germany) · DEUniversities of Giessen and Marburg Lung Center · DEPhilipps University of Marburg · DE

Funding

German Federal Ministry of Education and Research, the German Center for Lung Research (DZL) FKZ82DZL40502 and FKZ82DZLC15A2
6 · The paper itself

Abstract

backgroundA subset of COPD-patients presents with eosinophilic airway inflammation. While treatment of asthmatic patients with the GATA3-specific DNAzyme SB010 attenuated sputum eosinophilia after allergen challenge, this specific treatment has not been evaluated in patients with COPD. Our objective was to evaluate the feasibility and safety of inhaled SB010 in COPD patients with sputum eosinophilia.

methodsWe conducted a randomized, double-blind, placebo-controlled, multicentre clinical trial in COPD-patients with sputum eosinophilia (≥2.5% non-squamous cells). Patients inhaled 10 mg SB010 bid or matching placebo via the controlled inhalation system AKITA2 APIXNEB for 28 days. Endpoints included the feasibility of the study (primary), patient's safety, sputum eosinophils, F

resultsOne hundred thirty patients were screened, 23 patients were randomized (FEV

conclusionIn patients with eosinophilic COPD, sputum eosinophils could be reduced by inhalation of SB010. Long-term studies are needed to demonstrate clinical efficacy.

Indexed as

Administration, InhalationAgedDNA, CatalyticDouble-Blind MethodEosinophilsFeasibility StudiesFemaleGATA3 Transcription FactorHumansMaleMiddle AgedPulmonary Disease, Chronic ObstructivePulmonary EosinophiliaSputumDNA, CatalyticGATA3 protein, humanGATA3 Transcription FactorCOPDDNAzymeEosinophilsSB010SputumT-helper-2-cells

Identifiers

PMID29615049
PMCPMC5883532
OpenAlexW2796200794

What OpenQuestion holds

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LicenceCC BY
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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.