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Clinical Trials/NCT02801981
NCT02801981
Completed
Phase 1

A Double-blind, Randomized, Placebo Controlled, Dose Escalating Crossover Study to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Parameters of Single Doses of GSK2330672 in Japanese Healthy Male Volunteers

GlaxoSmithKline1 site in 1 country16 target enrollmentJune 2016

Overview

Phase
Phase 1
Intervention
GSK2230672
Conditions
Cholestasis
Sponsor
GlaxoSmithKline
Enrollment
16
Locations
1
Primary Endpoint
Safety as assessed by body temperature
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study will be the first to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics following single dose of 10 milligrams (mg) to 180 mg of GSK2330672 in Japanese healthy subjects. This is a double-blind, randomized, placebo-controlled, dose-escalating and incomplete block crossover study to be conducted in 16 Japanese healthy subjects. Study will be conducted in four periods; subjects will receive either placebo or GSK2330672 (10 mg, 30 mg, 90 mg or 180 mg based on randomization) in each treatment period. Each period will be separated by washout period (at least 6 days from dosing). Total duration of study for each subject will be approximately 5 weeks from the first dosing to follow up visit.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
August 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Japanese male aged between 20 and 64 years of age inclusive, at the time of signing the informed consent
  • Healthy as determined by the investigator or medically qualified designee based on a medical evaluation including medical history, physical examination, laboratory tests and 12-lead ECG. A subject with a clinical abnormality or laboratory parameter(s) which is/are not specifically listed in the inclusion or exclusion criteria, outside the reference range for the population being studied may be included only if the investigator (in consultation with the Medical Monitor if required) agree and document that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
  • Regular bowel movement \>=1 per two days.
  • Body weight \>= 50 kilogram and body mass index (BMI) is more than or equal to 18.5 kilogram / square meter (kg/m\^2) and less than 25.0 kg/m\^2
  • Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the consent form and in this protocol.

Exclusion Criteria

  • Alanine transaminase (ALT) and/or bilirubin \>1.5x Upper limit of normal (ULN) (isolated bilirubin \>1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin \<35%).
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome)
  • QT interval corrected for heart rate according to Fridericia's formula (QTcF) \> 450 millisecond (msec)
  • Current or chronic history of inflammatory bowel disease, chronic diarrhea, Crohn's disease or malabsorption syndromes.
  • Current or chronic history of cholelithiasis, inflammatory gall bladder disease, cholestatic liver injury, and cholecystecomy.
  • Fecal occult blood test positive at screening.
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (includes St. John's Wort) within 14 days or 5 half-lives, whichever is longer, prior to the first dose of study medication.
  • History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of \>14 drinks. One drink is equivalent to 12 grams (g) of alcohol: 350 millilitre (mL) of beer, 150 mL of wine or 45 mL of 80 proof distilled spirits.
  • History or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.
  • History of sensitivity to heparin or heparin-induced thrombocytopenia.

Arms & Interventions

Sequence 1: GSK2230672 10mg, 30mg, 90mg, and Placebo

Subjects will receive GSK2230672 10 mg in period 1, GSK2230672 30 mg in Period 2, GSK2230672 90 mg in Period 3 and placebo in period 4.

Intervention: GSK2230672

Sequence 1: GSK2230672 10mg, 30mg, 90mg, and Placebo

Subjects will receive GSK2230672 10 mg in period 1, GSK2230672 30 mg in Period 2, GSK2230672 90 mg in Period 3 and placebo in period 4.

Intervention: Placebo

Sequence 2:GSK2230672 10mg, 30mg, Placebo, and GSK2230672 90mg

Subjects will receive GSK2230672 10 mg in period 1, GSK2230672 30 mg in Period 2, placebo in period 3, and GSK2230672 90 mg in period 4.

Intervention: GSK2230672

Sequence 2:GSK2230672 10mg, 30mg, Placebo, and GSK2230672 90mg

Subjects will receive GSK2230672 10 mg in period 1, GSK2230672 30 mg in Period 2, placebo in period 3, and GSK2230672 90 mg in period 4.

Intervention: Placebo

Sequence 3:GSK2230672 10mg, Placebo, GSK2230672 90mg and 180mg

Subjects will receive GSK2230672 10 mg in period 1, placebo in Period 2, GSK2230672 90 mg in Period 3 and GSK2230672 180 mg in period 4.

Intervention: GSK2230672

Sequence 3:GSK2230672 10mg, Placebo, GSK2230672 90mg and 180mg

Subjects will receive GSK2230672 10 mg in period 1, placebo in Period 2, GSK2230672 90 mg in Period 3 and GSK2230672 180 mg in period 4.

Intervention: Placebo

Sequence 4: Placebo, GSK2230672 30mg, 90mg and 180mg

Subjects will receive placebo in period 1, GSK2230672 30 mg in Period 2, GSK2230672 90 mg in Period 3 and GSK2230672 180 mg in period 4.

Intervention: GSK2230672

Sequence 4: Placebo, GSK2230672 30mg, 90mg and 180mg

Subjects will receive placebo in period 1, GSK2230672 30 mg in Period 2, GSK2230672 90 mg in Period 3 and GSK2230672 180 mg in period 4.

Intervention: Placebo

Outcomes

Primary Outcomes

Safety as assessed by body temperature

Time Frame: Maximum of 5 weeks

Body temperature will be measured on Day -1, post dose 2 hrs, 12.5 hrs, 24.5 hrs and at 48 hrs in each period and at follow-up.

Safety as assessed by clinical chemistry parameters

Time Frame: Maximum of 5 weeks

Blood sample will be collected on Day -1, at 48 hrs in each period and at follow-up

Number of Subjects with Adverse events (AE)

Time Frame: Maximum of 5 weeks

Safety as assessed by blood pressure

Time Frame: Maximum of 5 weeks

Systolic and diastolic blood pressure will be measured on Day -1, post dose 2 hours (hrs), 12.5 hrs, 24.5 hrs and at 48 hrs in each period and at follow-up.

Safety as assessed by heart rate

Time Frame: Maximum of 5 weeks

Heart rate will be measured on Day -1, post dose 2 hrs, 12.5 hrs, 24.5 hrs and at 48 hrs in each period and at follow-up.

Safety as assessed by haematology

Time Frame: Maximum of 5 weeks

Blood sample will be collected on Day -1, at 48 hrs in each period and at follow-up

Safety as assessed by fecal occult blood

Time Frame: Maximum of 5 weeks

Fecal occult blood testing will be conducted on Screening (2 samples during Screening period) and each dosing period (anytime from dosing to next dose).

Safety as assessed by Electrocardiogram (ECG)

Time Frame: Maximum of 5 weeks

Electrocardiogram will be measured on Day -1, post dose 2 hrs, 12.5 hrs, 24.5 hrs and at 48 hrs in each period and at follow-up.

Safety as assessed by urinalysis

Time Frame: Maximum of 5 weeks

Sample will be collected on Day -1, at 48 hrs in each period and at follow-up

Secondary Outcomes

  • Plasma concentration of GSK2330672(Blood samples will be collected predose and post dose at 0.5 hrs, 2 hr, 3.5 hr, 5 hr on Day 1 of each period)

Study Sites (1)

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