Dose-escalation Study of GSK2330672 in Japanese Healthy Male Volunteers
- Conditions
- Cholestasis
- Interventions
- Drug: GSK2230672Drug: Placebo
- Registration Number
- NCT02801981
- Lead Sponsor
- GlaxoSmithKline
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 16
- 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.
- 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.
- History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or Medical Monitor, contraindicates their participation
- A positive pre-study syphilis, Hepatitis B surface antigen, Hepatitis C antibody, Human Immunodeficiency Virus (HIV) antigen antibody or Human T-cell Lymphotropic Virus-1 (HTLV-1) antibody result of screening
- A positive pre-study urine drug screen.
- History of donation of blood or blood products >= 400 mL within 3 months or >= 200 mL within 1 month prior to screening.
- The subject has participated in a clinical trial and has received an investigational product within four months or 5 half-lives (whichever is longer) prior to the dosing day in the current study
- Exposure to more than four new chemical entities within 12 months prior to the dosing day.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Sequence 1: GSK2230672 10mg, 30mg, 90mg, and Placebo GSK2230672 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. Sequence 1: GSK2230672 10mg, 30mg, 90mg, and Placebo 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. Sequence 2:GSK2230672 10mg, 30mg, Placebo, and GSK2230672 90mg GSK2230672 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. Sequence 2:GSK2230672 10mg, 30mg, Placebo, and GSK2230672 90mg Placebo 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. Sequence 3:GSK2230672 10mg, Placebo, GSK2230672 90mg and 180mg GSK2230672 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. Sequence 3:GSK2230672 10mg, Placebo, GSK2230672 90mg and 180mg Placebo 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. Sequence 4: Placebo, GSK2230672 30mg, 90mg and 180mg GSK2230672 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. Sequence 4: Placebo, GSK2230672 30mg, 90mg and 180mg Placebo 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.
- Primary Outcome Measures
Name Time Method Safety as assessed by body temperature 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 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) Maximum of 5 weeks Safety as assessed by blood pressure 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 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 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 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) 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 Maximum of 5 weeks Sample will be collected on Day -1, at 48 hrs in each period and at follow-up
- Secondary Outcome Measures
Name Time Method 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
Trial Locations
- Locations (1)
GSK Investigational Site
🇯🇵Tokyo, Japan