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Clareo Health | Dose-ranging Study of Vilanterol (VI) Inhalation Powder in Children

Dose-ranging Study of Vilanterol (VI) Inhalation Powder in Children

NCT01573767·120 sites·ClinicalTrials.gov

What this study is about

Take this into the appointment.

Saves the questions and what to expect into your notes, next to the visit they belong to.

Keep this study

Lead

GlaxoSmithKline

Age

5–11

Sex

ALL

Healthy volunteers

Not accepted

You may be eligible if

Written informed consent from at least one parent/ legal guardian to take part in the study.:
Diagnosis of asthma
pre-bronchodilator PEF between ≥50% to ≤90% of their best post-bronchodilator value
Receiving stable asthma therapy of short acting beta-agonist (SABA) plus ICS (total daily dose FP 200mcg or equivalent)

You may not be if

history of life-threatening asthma
history of asthma exacerbation for asthma within 6 months prior to screening.
Culture-documented or suspected bacterial or viral infection
significant abnormality or medical condition
Present use of any tobacco products

The record

StatusCompleted

PhasePhase 2

Taking part463

StartedApr 2012

UpdatedJan 9, 2017

Conditions

Where120

GSK Investigational Site
Birmingham, Alabama, United States
GSK Investigational Site
Mobile, Alabama, United States
GSK Investigational Site
Little Rock, Arkansas, United States