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A Study to Evaluate the Effect of Two Different Repeat Doses of GSK2190915 on the QTc Interval.

This study has been withdrawn prior to enrollment.
(Study was terminated due to toxicology findings after screening started but before first subject first dose.)
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT01721135
First received: November 1, 2012
Last updated: August 20, 2013
Last verified: August 2013

November 1, 2012
August 20, 2013
September 2010
December 2014   (final data collection date for primary outcome measure)
Change from baseline in QTcF interval at each timepoint on Day 5 (average of at least 3 12-lead Holter ECG replicates per time point) for 100mg GSK2190915 as compared with time-matched placebo [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01721135 on ClinicalTrials.gov Archive Site
  • Change from baseline in QTcF interval at each timepoint on Day 5 (average of at least 3 12-lead Holter ECG replicates per time point) for 1000mg GSK2190915 as compared with time-matched placebo [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Change from baseline in QTcB interval at each timepoint on Day 5 (average of at least 3 12-lead Holter ECG replicates per time point) for 100mg and 1000mg GSK2190915 as compared with time-matched placebo [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Change from baseline in QTcF interval at each timepoint on Day 5 (average of at least 3 12-lead Holter ECG replicates per time point) for moxifloxacin as compared with time-matched placebo [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Plasma concentrations of GSK2190915 taken on Day 5 to derive pharmacokinetic parameters including Maximum observed concentration (Cmax), Time of occurrence of Cmax (tmax) and Area under the concentration-time curve over the dosing interval (AUC(0-τ)) [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Heart rate and ECG parameters taken on Day 1 and Day 5 compared with concentration of Plasma GSK2190915 to find relationship [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Maximal change from baseline on Day 5 for QTcF and QTcB [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Change from baseline at each timepoint on Day 5 for other cardiac electrophysiological parameters: QT, QRS, RR, PR and ventricular rate [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
  • Assessment of safety and tolerability of GSK2190915 by 12-lead ECGs, vital signs, adverse events and clinical laboratory tests throughout treatment period [ Time Frame: 5 days ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
A Study to Evaluate the Effect of Two Different Repeat Doses of GSK2190915 on the QTc Interval.
A Randomised, Placebo Controlled, Four-way Cross-over Study to Assess Cardiac Re-polarisation Following Repeat Dosing With GSK2190915 and Placebo for Five Days, With Moxifloxacin as a Positive Control, in Healthy Male and Female Subjects.

This study is a randomized, placebo controlled, four way crossover, in which the the effect of GSK2190915 on the QTc interval is assessed. Healthy subjects will recieve a 5 day course of each of the following; oral placebo, GSK2190915 100mg, GSK2190915 1000mg and moxifloxacin 400mg (single dose) with a weeks washout prior to starting the next course. Key assessments include a 12- lead electrocardiogram and pharmacokinetic testing. Safety will be assessed by blood pressure, heart rate, clinical laboratory safety tests and collection of adverse events .

This is a randomized, placebo controlled, four way crossover thorough QT study to evaluate the effect of repeat dose GSK2190915 on the QTc interval in healthy male and female subjects. Approximately 48 subjects will receive oral placebo, GSK2190915 (100mg or 1000mg) and moxifloxacin (400mg). GSK2190915 or matching placebo will be given once daily for 5 days with a moxifloxacin matching placebo given on Day 5. Moxifloxacin (positive control) will be given as a single-blind single dose on Day 5 with placebo administered on Days 1-4. Individual time-matched changes from baseline in QTcF (difference from placebo) for GSK2190915 will be determined 0-24 hours after dosing on Day 5 (primary endpoint). Secondary endpoints will include changes from baseline in QTcF, QTcB and QT interval at each timepoint after 5 days dosing of GSK2190915 and single dose moxifloxacin (400mg). Plasma concentrations on Day 5 (0-24 hours) and pharmacokinetic parameters of GSK2190915 will also be derived.

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Asthma
  • Drug: GSK2190915 100mg
    Film coated oral tablet
  • Drug: GSK2190915 200mg
    Film coated oral tablet
  • Drug: moxifloxacin 400mg
    Film coated oral tablet
  • Drug: moxifloxacin placebo
    Film coated oral tablet
  • Drug: GSK2190915 placebo
    Film coated oral tablet
  • Experimental: GSK2190915 100mg
    GSK2190915 100mg on days 1-5; moxifloxacin placebo on day 5
    Interventions:
    • Drug: GSK2190915 100mg
    • Drug: moxifloxacin placebo
    • Drug: GSK2190915 placebo
  • Experimental: GSK2190915 1000mg
    GSK2190915 1000mg on days 1-5; moxifloxacin placebo on day 5
    Interventions:
    • Drug: GSK2190915 200mg
    • Drug: moxifloxacin placebo
  • Active Comparator: moxifloxacin 400mg
    placebo tablet on days 1-5; moxifloxacin 400mg on day 5
    Interventions:
    • Drug: moxifloxacin 400mg
    • Drug: GSK2190915 placebo
  • Placebo Comparator: placebo
    placebo tablet on days 1-5; moxifloxacin placebo on day 5
    Interventions:
    • Drug: moxifloxacin placebo
    • Drug: GSK2190915 placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
December 2014
December 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or female between 18 and 65 years of age inclusive
  • Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), alkaline phosphatase and bilirubin ≤ 1.5x Upper limit of normal (ULN)
  • Healthy as determined by a physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring.
  • A female subject is eligible to participate if she is of: Non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy; or postmenopausal . Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods. Those of child-bearing potential must agree to use one of the protocol contraception methods.
  • Body mass index (BMI) within the range 18.5-29.0 kg/m2 (inclusive)
  • Capable of giving written informed consent
  • Current non-smokers who have not used tobacco products in the 6 month period preceding screening
  • No significant abnormality on 12-lead electrocardiogram (ECG) at screening
  • A 24 hour Holter ECG at screening that demonstrates no clinically significant abnormalities

Exclusion Criteria:

  • A physician deems the subject unsuitable for the study
  • A screening Holter ECG tracing that reveals clinically concerning arrhythmias
  • A blood pressure that is persistently higher than 140/90 millimetres of mercury (mmHg) at screening.
  • A mean heart rate outside the range 40-90 beats per minute (bpm) at screening.
  • History or presence of any medically significant disease, or any disorder. In particular, a family history of QT prolongation, of early or sudden cardiac death or of early cardiovascular disease.
  • A positive result for Hepatitis B or Hepatitis C within 3 months of screening
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities
  • A positive pre-study drug/alcohol screen
  • A positive test for Human Immunodeficiency Virus (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 3 months of the first dosing day in the current study
  • Exposure to more than four new chemical entities within 12 months prior to the first dosing day
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements from 14 days before screening until the follow-up visit unless permitted by the investigator
  • 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 3 month period
  • Pregnant females
  • Lactating females
  • Unwillingness or inability to follow the procedures outlined in the protocol
  • Subject is mentally or legally incapacitated
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United Kingdom
 
NCT01721135
112360
No
GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
August 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP