Evidence map›Paper›PMID 28744115›Full record

Trial reportInternational journal of chronic obstructive pulmonary disease2017

Bronchodilator efficacy of extrafine glycopyrronium bromide: the Glyco 2 study.

Dave Singh, Mario Scuri, Sara Collarini, Stefano Vezzoli, Fabrizia Mariotti, Annamaria Muraro, Daniela Acerbi

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of chronic obstructive pulmonary disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01176903 (Randomized, Double-blind, Placebo-controlled, Cross-over Study to Investigate the Bronchodilator Efficacy and Safety After Single and Repeated Administrations of Different Doses of Glycopyrrolate Via pMDI in Moderate to Severe COPD Patients.), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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.

NCT01176903 phase1 / phase2completednot on this map

Randomized, Double-blind, Placebo-controlled, Cross-over Study to Investigate the Bronchodilator Efficacy and Safety After Single and Repeated Administrations of Different Doses of Glycopyrrolate Via pMDI in Moderate to Severe COPD Patients.

TypeinterventionalSponsorChiesi Farmaceutici S.p.A.Ran2010 to 2011Enrolled65ConditionsChronic Obstructive Pulmonary Disease (COPD)ArmsGlycopyrrolate, Tiotropium, placebo
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. 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

7 authors at 1 institution in 1 country.

Dave SinghMedicines Evaluation, University Of Manchester, University Hospital of South Manchester, Manchester, UK.
Mario ScuriGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Sara CollariniGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Stefano VezzoliGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Fabrizia MariottiGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Annamaria MuraroGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Daniela AcerbiGlobal Clinical Development, Chiesi Farmaceutici SpA, Parma, Italy.
Chiesi (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An extrafine formulation of the long-acting muscarinic antagonist glycopyrronium bromide (GB) is in development for chronic obstructive pulmonary disease (COPD), in combination with beclometasone dipropionate and formoterol fumarate - a "fixed triple". This two-part study was randomized, double blind, placebo controlled in patients with moderate-to-severe COPD: Part 1: single-dose escalation, GB 12.5, 25, 50, 100 or 200 μg versus placebo; Part 2: repeat-dose (7-day), four-period crossover, GB 12.5, 25 or 50 μg twice daily (BID) versus placebo, with an open-label extension in which all patients received tiotropium 18 μg once daily. On the morning of Day 8 in all five periods, patients also received formoterol 12 μg. In study Part 1, 27 patients were recruited. All GB doses significantly increased from baseline forced expiratory volume in 1 second (FEV

Indexed as

Administration, InhalationAdrenergic beta-2 Receptor AgonistsAdultAgedAlbuterolBronchodilator AgentsCross-Over StudiesDouble-Blind MethodDrug Therapy, CombinationEnglandFemaleForced Expiratory VolumeGlycopyrrolateHumansIpratropiumLungAdrenergic beta-2 Receptor AgonistsAlbuterolBronchodilator AgentsGlycopyrrolateIpratropiumMuscarinic AntagonistsTiotropium BromidebronchodilatorCOPDdose-rangingglycopyrronium

Identifiers

PMID28744115
PMCPMC5511020
OpenAlexW2727679611

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.