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A Study in Asthmatics to Determine the Efficacy and Dose Response of Repeat Doses of GW870086X on Forced Expiratory Volume in 1 Second (FEV1)

30. November 2016 aktualisiert von: GlaxoSmithKline

A Phase II Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Multicentre Study to Determine the Efficacy and Dose Response of Repeat Inhaled Doses of GW870086X on FEV1 in Adults With Persistent Asthma

This is a randomised, double-blind, placebo-controlled, parallel group study to determine the efficacy of twenty-seven day- repeat inhaled daily doses of GW870086X on forced expiratory volume in 1 second (FEV1). Initially there will be 3 treatment arms; placebo, 2mg GW870086X and 4mg GW870086X. After an interim analysis the trial may; continue to completion using the original doses, be terminated early, or have a fourth arm added of either 1mg GW870086X once daily or 3mg GW870086X once daily.

Studienübersicht

Detaillierte Beschreibung

This is a randomised, double-blind, placebo-controlled, parallel group study to determine the efficacy of twenty-seven day- repeat inhaled doses of GW870086X on FEV1. GW870086X is a novel inhaled corticosteroid with potent glucocorticoid activity currently in development by GlaxoSmithKline (GSK) as an inhaled treatment of persistent asthma. Initially, subjects will be randomised to receive placebo, 2mg or 4mg GW870086X once daily. An interim analysis will be performed on the primary endpoint to potentially adapt the study design after approximately 45 subjects have completed dosing. Based on the results of the interim analysis, the trial may continue to completion using the original doses or an adaptation to the doses could be made. Either the 1mg GW870086X once daily arm or 3mg GW870086X once daily arm may be added, or the trial could be terminated early. After screening there will be a 4 week run in period prior to start of treatment and after will be a follow up period 1-2 weeks after last dose. Approximately 120 subjects will complete the study. Key safety assessments include; clinical laboratory tests, vital signs and collection of adverse events (AE's).

Studientyp

Interventionell

Einschreibung (Tatsächlich)

136

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Sofia, Bulgarien, 1612
        • GSK Investigational Site
      • Berlin, Deutschland, 14050
        • GSK Investigational Site
      • Berlin, Deutschland, 10969
        • GSK Investigational Site
      • Hamburg, Deutschland, 20354
        • GSK Investigational Site
    • Hessen
      • Frankfurt, Hessen, Deutschland, 60596
        • GSK Investigational Site
    • Niedersachsen
      • Hannover, Niedersachsen, Deutschland, 30625
        • GSK Investigational Site
    • Sachsen-Anhalt
      • Magdeburg, Sachsen-Anhalt, Deutschland, 39112
        • GSK Investigational Site
    • Schleswig-Holstein
      • Luebeck, Schleswig-Holstein, Deutschland, 23552
        • GSK Investigational Site
      • Bloemfontein,, Südafrika, 9301
        • GSK Investigational Site
      • George, Südafrika, 6529
        • GSK Investigational Site
      • Newton Park, Port Elizabeth, Südafrika, 6045
        • GSK Investigational Site

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 65 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Male or female between 18 and 65 years
  • A female subject is eligible to participate if she is of: Non-childbearing potential. Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to discontinue HRT to allow confirmation of post-menopausal status prior to study enrollment.
  • Male subjects must agree to use one of the protocol contraception methods.
  • Body weight, men ≥ 50 kg, women ≥ 45 kg and BMI within the range 18.5 - 29.0 kg/m2 (inclusive).
  • Documented history of bronchial asthma, first diagnosed at least 6 months prior to the screening visit and currently being treated only with intermittent short-acting beta-2 agonist therapy
  • Severity of Disease: A best FEV1 of 60%-85% of the predicted normal value during the Visit 1 screening period.
  • No history of smoking within 6 months of the start of the study and with a total pack year history of ≤10 pack years
  • Capable of giving written informed consent
  • Single QTcB or QTcF < 450 msec; or QTc < 480 msec in subjects with Bundle Branch Block.
  • AST and ALT < 2xULN; alkaline phosphatase and bilirubin ≤ 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).

Exclusion Criteria:

  • A positive test for Hepatitis B or Hepatitis C antibody.
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities
  • The subject has a positive pre-study drug/alcohol screen unless a positive can be explained by the patients' medication.
  • Past or present disease, which as judged by the investigator, may affect the outcome of this study.
  • Clinically significant abnormalities in safety laboratory analysis at screening, as determined by the investigator.
  • Subject is hypertensive at screening.
  • History of life-threatening asthma, defined as an asthma episode that required intubation and/or was associated with hypercapnoea, respiratory arrest and/or hypoxic seizures.
  • Administration of oral, injectable or dermal steroids within 8 weeks of screening.
  • Exacerbation of asthma within 4 weeks prior to the first dose of study medication.
  • Respiratory Infection that is not resolved within the 4 weeks before screening and led to a change in asthma management, or in the opinion of the Investigator is expected to affect the subjects asthma status or the subjects ability to participate in the study.
  • Any asthma exacerbation requiring oral corticosteroids within 8 weeks of screening. A subject must not have had any hospitalisation for asthma within 6 months prior to screening
  • A positive test for HIV antibody.
  • History of regular alcohol consumption within 6 months of the study.
  • The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
  • Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
  • Use of prescription or non-prescription drugs within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety. Paracetamol is an exception and will be permitted at daily doses of up to 4 g from screening to follow-up.
  • Has taken Xanthines (including theophylline, but not including caffeine), anticholinergics, cromoglycates and/or long-acting beta-2 agonists within 1 week prior to screening and is unable to abstain from them throughout the study.
  • Unable to abstain from other medications other than short acting inhaled beta-2 agonists and paracetamol (up to 4 g per day) 7 days before screening until the follow-up visit.
  • Unable to abstain from medication or supplements that significantly inhibit the cytochrome P450 subfamily enzyme CYP3A4, from screening and throughout the study.
  • Unable to use the DISKHALER® device correctly.
  • History of sensitivity to any of the study medications.
  • Where participation in the study would result in donation of blood or blood products in excess of 500 ml within a 56 day period.
  • Unwillingness or inability to follow the procedures outlined in the protocol.
  • The subject is not able to understand or comply with protocol requirements, instructions and protocol stated restrictions.
  • Vulnerable subjects.
  • Subject is mentally or legally incapacitated.
  • Urinary cotinine levels indicative of smoking or history within 6 months prior to screening.
  • Consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices from 7 days prior to the first dose of study medication.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: GW870086 2mg
GW870086 2mg once daily in the morning for 27 ± 2 days
oral inhalation
Experimental: GW870086 4mg
GW870086 4mg once daily in the morning for 27 ± 2 days
oral inhalation
Placebo-Komparator: Placebo
Placebo once daily in the morning for 27 ± 2 days
oral inhalation
Experimental: GW870086 1mg
GW870086 1mg once daily in the morning for 27 ± 2 days
oral inhalation
Experimental: GW870086 3mg
GW870086 3mg once daily in the morning for 27 ± 2 days
oral inhalation

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Change from baseline associated with GW870086X versus placebo at Day 28 on FEV1
Zeitfenster: Day 28
Day 28

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Change from baseline in FEV1 on Day 7, Day 14 and Day 21
Zeitfenster: Days; 7, 14, 21
Days; 7, 14, 21
Change from baseline in peak expiratory flow rate (PEFR) measured twice daily over 28 days
Zeitfenster: Days 1-28
Days 1-28
Rescue medication usage
Zeitfenster: Days 1-28
Days 1-28
Assessment of vital signs, safety laboratory parameters and incidences of adverse events throughout treatment period
Zeitfenster: 9-10 weeks
9-10 weeks

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Dezember 2010

Primärer Abschluss (Tatsächlich)

1. Juli 2011

Studienabschluss (Tatsächlich)

1. August 2011

Studienanmeldedaten

Zuerst eingereicht

19. November 2010

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

19. November 2010

Zuerst gepostet (Schätzen)

22. November 2010

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

1. Dezember 2016

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

30. November 2016

Zuletzt verifiziert

1. November 2016

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

Ja

Beschreibung des IPD-Plans

Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Studiendaten/Dokumente

  1. Statistischer Analyseplan
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  2. Einwilligungserklärung
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  3. Studienprotokoll
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  4. Kommentiertes Fallberichtsformular
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  5. Einzelner Teilnehmerdatensatz
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  6. Datensatzspezifikation
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register
  7. Klinischer Studienbericht
    Informationskennung: 114749
    Informationskommentare: For additional information about this study please refer to the GSK Clinical Study Register

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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