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A Single Dose Of Compound SB-681323 Compared To Prednisolone On A Protein That Is an Indicator For Rheumatoid Arthritis

27. Juli 2017 aktualisiert von: GlaxoSmithKline

A Randomised, Placebo-controlled, Parallel Group Single Dose Study of SB681323 in Patients With Active RA to Investigate the CRP Dose Response Relationship

This study is designed to compare a range of doses of SB-681323 with prednisolone, which has known effects on rheumatoid arthritis patients. By comparing the two drugs and their effects on blood proteins that indicate for rheumatoid arthritis, we hope to ascertain information on the most effective dose of SB-681323 to use in future.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Arthritis, Rheuma

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Tatsächlich)

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

Australien
- New South Wales
  - Darlinghurst, New South Wales, Australien, 2010
    - GSK Investigational Site
- Queensland
  - Douglas, Queensland, Australien, 4814
    - GSK Investigational Site
  - Woolloongabba, Queensland, Australien, 4102
    - GSK Investigational Site
- South Australia
  - Daw Park, South Australia, Australien, 5041
    - GSK Investigational Site
  - Woodville, South Australia, Australien, 5011
    - GSK Investigational Site
- Tasmania
  - Hobart, Tasmania, Australien, 7000
    - GSK Investigational Site
- Western Australia
  - Shenton Park, Western Australia, Australien, 6008
    - GSK Investigational Site
Deutschland
- - Berlin, Deutschland, 14059
    - GSK Investigational Site
  - Berlin, Deutschland, 13125
    - GSK Investigational Site
  - Berlin, Deutschland, 14109
    - GSK Investigational Site
  - Berlin, Deutschland, 12163
    - GSK Investigational Site
- Baden-Wuerttemberg
  - Villingen-Schwenningen, Baden-Wuerttemberg, Deutschland, 78054
    - GSK Investigational Site
- Niedersachsen
  - Hildesheim, Niedersachsen, Deutschland, 31134
    - GSK Investigational Site
- Sachsen
  - Chemnitz, Sachsen, Deutschland, 09111
    - GSK Investigational Site
  - Leipzig, Sachsen, Deutschland, 04107
    - GSK Investigational Site
  - Leipzig, Sachsen, Deutschland, 04229
    - GSK Investigational Site
Frankreich
- - Montpellier Cedex 5, Frankreich, 34295
    - GSK Investigational Site
- Picardie
  - Amiens, Picardie, Frankreich, 80054
    - GSK Investigational Site
Russische Föderation
- - Ekaterinburg, Russische Föderation, 620102
    - GSK Investigational Site
  - Moscow, Russische Föderation, 115522
    - GSK Investigational Site
  - Ryazan, Russische Föderation, 390026
    - GSK Investigational Site
  - Yaroslavl, Russische Föderation, 150003
    - GSK Investigational Site
Vereinigtes Königreich
- - Oxford, Vereinigtes Königreich, OX3 7LP
    - GSK Investigational Site
  - Sheffield, Vereinigtes Königreich, S10 2RX
    - GSK Investigational Site
- Cambridgeshire
  - Cambridge, Cambridgeshire, Vereinigtes Königreich, CB2 0QQ
    - GSK Investigational Site
- Lancashire
  - Wigan, Lancashire, Vereinigtes Königreich, WN6 9EP
    - GSK Investigational Site
- Merseyside
  - Liverpool, Merseyside, Vereinigtes Königreich, L9 7AL
    - GSK Investigational Site
- Northumberland
  - Newcastle, Northumberland, Vereinigtes Königreich, NE1 4LP
    - 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 und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion criteria:

Must have a diagnosis of RA according to the revised 1987 criteria of the American College of Rheumatology.
Must have 3 or more swollen or 3 or more tender/painful joints at screening.
Must be on stable weekly methotrexate (2.5mg - 25mg) for at least eight weeks prior to screening.

Exclusion criteria:

Must not be morbidly obese.

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: Doppelt

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme	Maßnahmenbeschreibung	Zeitfenster
Analysis for C-Reactive protein (CRP) levels 72 hours post-dose following SB-681323 Zeitfenster: Day 3 (at 72 hour)	CRP levels were compared between SB-681323 and placebo 72 hours post-dose. The ratio of the dose response relationship of placebo and 7.5mg, 15mg and 25mg of SB-681323 has been presented.	Day 3 (at 72 hour)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme	Maßnahmenbeschreibung	Zeitfenster
Analysis of CRP levels 24 and 48 hours post-dose following SB-681323 Zeitfenster: Day 1 (at 24 hour) and Day 2 (at 48 hour)	CRP levels were compared between SB-681323 and placebo 24 and 48 hours post-dose. The ratio of the dose response relationship of placebo and 7.5mg, 15mg and 25mg of SB-681323 has been presented.	Day 1 (at 24 hour) and Day 2 (at 48 hour)
Analysis of Interleukin (IL)-6 levels up to 72 hours post-dose following SB-681323 Zeitfenster: Upto Day 3 (at 1, 3, 24 and 72 hour)	A blood sample of approximately 5 milliliter (mL) was taken for measurement of serum markers. IL-6 measurements were performed at 1 hour, 3, hours, 24 hours and 72 hours post-dose. The ratio of the dose response relationship of placebo and 7.5mg, 15mg and 25mg of SB-681323 has been presented.	Upto Day 3 (at 1, 3, 24 and 72 hour)
Number of participants with adverse events (AE) and serious adverse events (SAE) Zeitfenster: Upto Day 3 (72 hours)	An AE is defined as any untoward medical occurrence in a participant or clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a medicinal product. An SAE is defined as any untoward medical occurrence that, at any dose, results in death, is life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect, may jeopardize the participant or require medical or surgical intervention to prevent one of the other outcomes listed in the definition above, or is an event of possible drug-induced liver injury. There were no SAEs reported in this study.	Upto Day 3 (72 hours)
Change from Baseline in vital sign systolic blood pressure (SBP) and diastolic blood pressure (DBP) Zeitfenster: Baseline (at pre-dose Day 0) and Day 3 (at 90 minutes, 3 hour, 24 and 72 hour)	Supine vital signs SBP and DBP were recorded whilst the participant was in a supine position (participant lying flat with maximum one pillow) having rested in that position for at least 10 minutes before each reading. Measurements were performed at 90 minutes, 3 hours, 24 hours and 72 hours post-dose. Baseline was defined as assessment performed pre-dose at Day 0. Change from Baseline was calculated by subtracting the Baseline value from the individual post-randomization values at the time of assessment.	Baseline (at pre-dose Day 0) and Day 3 (at 90 minutes, 3 hour, 24 and 72 hour)
Change from Baseline in vital sign heart rate Zeitfenster: Baseline (at pre-dose Day 0) and Day 3 (at 90 minutes, 3 hour, 24 and 72 hour)	Supine vital signs (heart rate) was recorded whilst the participant was in a supine position (participant lying flat with maximum one pillow) having rested in that position for at least 10 minutes before each reading. Measurements were performed at 90 minutes, 3 hours, 24 hours and 72 hours post-dose. Baseline was defined as assessment performed pre-dose at Day 0. Change from Baseline was calculated by subtracting the Baseline value from the individual post-randomization values at the time of assessment.	Baseline (at pre-dose Day 0) and Day 3 (at 90 minutes, 3 hour, 24 and 72 hour)
Number of participants with abnormal electrocardiogram (ECG) findings Zeitfenster: Day 1 (pre-dose, 1 hour and 3 hour)	Full 12-lead ECGs were recorded using an ECG machine that automatically calculated the pulse rate and measured PR, RR, QRS, QT, QTc(b) intervals (Bazett's correction was applied to QTc measurements). Measurements were carried out at pre-dose, 1 hour and 3 hours on Day 1. ECG findings were characterized as abnormal-not clinically significant (A-NCS) and abnormal-clinically significant (A-CS). Data has been presented for A-NCS findings on Day 1.	Day 1 (pre-dose, 1 hour and 3 hour)
Number of participants with clinical chemistry data outside the clinical concern range Zeitfenster: Upto Day 3 (pre-dose, 24, 48 and 72 hours	Clinical chemistry parameters included albumin, alkaline phosphatase, alanine amino transferase, indirect bilirubin, calcium, chloride, creatinine, gamma glutamyl transferase, glucose, potassium, lactate dehydrogenase, triglycerides. Measurements were carried out at pre-dose, 24 hours, 48 hours and 72 hours. Data for number of participants with values outside clinical concern range defined as high and low have been presented.	Upto Day 3 (pre-dose, 24, 48 and 72 hours
Number of participants with hematology data outside the clinical concern Zeitfenster: Upto Day 3 (pre-dose, 24 and 72 hours)	Hematology parameters included eosinophils, hemoglobin, hematocrit, lymphocytes, mean corpuscle hemoglobin, mean corpuscle volume, platelet count, reticulocytes, white blood cell count (WBC). Measurements were carried out at pre-dose, 24 hours and 72 hours. Data for number of participants with values outside clinical concern range defined as high and low have been presented.	Upto Day 3 (pre-dose, 24 and 72 hours)
Number of participants with abnormal urinalysis dipstick results Zeitfenster: Upto Day 3 (pre-dose, 24 and 72 hours)	Approximately 10-20 mL mid-stream urine was collected into a sterile container and was screened by dipstick for: occult blood, proteins, ketones, glucose, red blood cells (RBC) and WBC. Sediment microscopy was performed only if any of the Multi-stick tests were abnormal. In such cases, microscopy was performed for: WBC, RBC, hyaline casts, granular casts, cellular casts. Data for number of participants with abnormal urinalysis results for positive parameters as assessed by dipstick and microscopic analysis have been presented.	Upto Day 3 (pre-dose, 24 and 72 hours)
Whole blood messenger RNA (mRNA) levels of tumor necrosis factor alpha [TNF-α], IL-8, IL-1β and Cyclo-oxygenase-2 [COX-2] (and other genes implicated in the pathogenesis of RA or genes involved in the mode of action of the compounds administered) Zeitfenster: Pre-dose, 45 minutes, 90 minutes and 3 hours on Day 1	Blood samples were taken for extraction of whole blood mRNA (2 x 2.5mL PAXgene tubes). The samples were taken at the time-points pre-dose, 45 minutes, 90 minutes and 3 hours. Messenger RNA levels for various markers was measured. These markers included Prednisolone markers: DDIT4, DUSP1, FKBP5, GILZ, IL1R2, TXNIP, ZNF145 and p38 markers: COX2, IFI30, IL1b, IL6, IL8, TNF. An aliquot of mRNA was stored for later analysis of other genes associated with the pathogenesis of RA and in the mode of action of the compounds administered.	Pre-dose, 45 minutes, 90 minutes and 3 hours on Day 1

Mitarbeiter und Ermittler

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

Sponsor

GlaxoSmithKline

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 (Tatsächlich)

21. Juni 2005

Primärer Abschluss (Tatsächlich)

3. August 2006

Studienabschluss (Tatsächlich)

3. August 2006

Studienanmeldedaten

Zuerst eingereicht

24. August 2005

Zuerst eingereicht, das die QC-Kriterien erfüllt hat