Evidence map›Paper›PMID 32393215›Full record

Trial reportBMC pulmonary medicine2020

Efficacy of revefenacin, a long-acting muscarinic antagonist for nebulized therapy, in patients with markers of more severe COPD: a post hoc subgroup analysis.

James F Donohue, Edward Kerwin, Chris N Barnes, Edmund J Moran, Brett Haumann, Glenn D Crater

2 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in BMC pulmonary medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 40% 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.

NCT02459080 phase3completednot on this map

A Phase 3, 12-week, Randomized, Double-blind Placebo-controlled Parallel Group Study of Nebulized TD-4208 in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorMylan Inc.Ran2015 to 2016Enrolled619ConditionsChronic Obstructive Pulmonary Disease (COPD)ArmsTD-4208, Placebo
NCT02512510 phase3completednot on this map

A Phase 3, 12-week, Randomized, Double-blind Placebo-controlled Parallel Group Study of Nebulized TD-4208 in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorMylan Inc.Ran2015 to 2016Enrolled611ConditionsChronic Obstructive Pulmonary Disease (COPD)ArmsTD-4208, Placebo
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Revefenacin Area Under the Curve Spirometry in Patients with Moderate to Very Severe COPD.International journal of chronic obstructive pulmonary disease · 2024
    Trial
  2. Article
  3. Article
  4. Revefenacin, a once-daily, long-acting muscarinic antagonist, for nebulized maintenance therapy in patients with chronic obstructive pulmonary disease.American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists · 2021
    Review
  5. Review
  6. Revefenacin: A Once-Daily, Long-Acting Bronchodilator For Nebulized Treatment Of COPD.International journal of chronic obstructive pulmonary disease · 2019
    Review
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

6 authors at 3 institutions in 1 country.

James F DonohuePulmonary Medicine, UNC School of Medicine, 321 S Columbia St, Chapel Hill, NC, 27516, USA.
Edward KerwinClinical Research Institute of Southern Oregon, LLC, 3860 Crater Lake Ave, Medford, OR, 97504, USA.
Chris N BarnesTheravance Biopharma US, Inc., 901 Gateway Blvd, South San Francisco, CA, 94080, USA.
Edmund J MoranTheravance Biopharma US, Inc., 901 Gateway Blvd, South San Francisco, CA, 94080, USA.
Brett HaumannTheravance Biopharma US, Inc., 901 Gateway Blvd, South San Francisco, CA, 94080, USA.
Glenn D CraterTheravance Biopharma US, Inc., 901 Gateway Blvd, South San Francisco, CA, 94080, USA. gcrater@theravance.com.
Theravance Biopharma (United States) · USClinical Research Institute · USUniversity of North Carolina Health Care · US

Funding

Theravance Biopharma Ireland Limited Not applicable
6 · The paper itself

Abstract

backgroundRevefenacin, a once-daily, long-acting muscarinic antagonist delivered via standard jet nebulizer, increased trough forced expiratory volume in 1 s (FEV

methodsA post hoc subgroup analysis of two replicate, randomized, phase 3 trials was conducted over 12 weeks. Endpoints included least squares change from baseline in trough FEV

resultsRevefenacin demonstrated significant improvements in FEV

conclusionsRevefenacin showed significantly greater improvements in FEV

trial registrationClinical trials registered with www.clinicaltrials.gov (Studies 0126 [NCT02459080; prospectively registered 22 May 2015] and 0127 [NCT02512510; prospectively registered 28 July 2015]).

Indexed as

Administration, InhalationAgedAged, 80 and overBenzamidesBronchodilator AgentsCarbamatesDose-Response Relationship, DrugDouble-Blind MethodFemaleForced Expiratory VolumeHumansLungMaleMiddle AgedMuscarinic AntagonistsPulmonary Disease, Chronic ObstructiveBenzamidesBronchodilator AgentsCarbamatesMuscarinic AntagonistsrevefenacinCOPDEfficacyLong-acting muscarinic antagonistNebulized therapyRevefenacin

Identifiers

PMID32393215
PMCPMC7216337
OpenAlexW3024372630

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.