ConductScience.org, home

Trial · NCT01471665

GSK2190915 Neutrophilic Asthma Study

NCT01471665, Phase 2, Completed, GlaxoSmithKline

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. GSK2190915 Neutrophilic Asthma Study. Trials, record NCT01471665. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01471665

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
GSK2190915 Neutrophilic Asthma Study
NCT number
NCT01471665
Status
Completed
Phases
Phase 2
Enrollment
14 participants, actual
Lead sponsor
GlaxoSmithKline
Conditions
Asthma
Interventions
GSK2190915 100mg, Placebo
First posted
2011-11-16
Last updated
2016-11-22

Source ClinicalTrials.gov

Registered outcomes8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryThe numbers of neutrophils in induced sputum in asthmatic subjects (average of absolute and percentage count on Visit 4 and Visit 5)13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailyPharmacodynamics
SecondaryThe levels of LTE4 in urine, LTB4-glucuronide in urine and LTB4 in sputum supernatant in asthmatic subjectsOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailyPharmacodynamics
SecondaryThe levels of high sensitive C-reactive protein (hsCRP) and other biomarkers (for example IL-17) in blood in asthmatic subjectsOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailyPharmacodynamics
SecondaryChanges in symptoms in asthmatic subjects compared to placebo using the asthma control questionnaireOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailySafety and tolerability and efficacy
SecondaryChanges in lung function as measured by Forced Expiratory Volume in one second (FEV1) in subjects with asthmaOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailySafety and tolerability and efficacy
SecondaryPlasma concentrations of GSK2190915 following repeated doses in asthmatic subjectsOn days 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailyPharmacokinetics
SecondaryIncidence of treatment emergent adverse events in asthmatic subjects and vital signs, electrocardiograms and safety laboratory parameters in asthmatic subjectsOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailySafety and tolerability and effiacy
SecondaryThe levels of biomarkers in sputum supernatant, for example IL-17, IL-8, neutrophil elastase and myeloperoxidase, as samples permit, in asthmatic subjectsOver 13 - 16 days post treatment with 100mg GSK2190915 or placebo once dailyPharmacodynamics

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
24333186DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01471665

GET https://conductscience.org/api/trials/v1/NCT01471665/registered