Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single, Oral Escalating Doses of GSK2647544 in Healthy Volunteers

Alzheimer's Disease Clinical Trial

Official title:

A Single-Blind, Randomized, Placebo-Controlled Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single, Oral Escalating Doses of GSK2647544 in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01702467
• Other study ID #: 116698
• Status: Completed
• Phase: Phase 1
• First received: October 4, 2012
• Last updated: October 16, 2017
• Start date: October 19, 2012
• Est. completion date: May 15, 2013

Study information

• Verified date: October 2017
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The current study will examine the safety, tolerability, plasma pharmacokinetics (PK), and plasma pharmacodynamics (PD) of single-doses of GSK2647544.The study will be conducted as a randomized, single-blind, placebo controlled, 4-way crossover single oral ascending dose design in 2 independent cohorts, eight healthy male subjects in each of the cohorts. Each potential subject will undergo Screening visit, Treatment Phase and Follow-up visit.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: May 15, 2013
• Est. primary completion date: May 15, 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Healthy males who are 18 to 55 years of age, inclusive

• Healthy as determined by a responsible and experienced physician

• aspartate aminotransferase (AST), Alanine transaminase (ALT), alkaline phosphatase and bilirubin <= 1.5xUpper Limit of Normal (ULN)

• Average of triplicate QTcB values and average of triplicate QTcF values must both < 450 millisecond (msec)

• Body weight > 50 kg (110 pounds) and body mass index (BMI) between 19 and 30

• Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods

• Capable of giving written informed consent

Exclusion Criteria:

• Those with Lp-PLA2 activity <=20 nanomole/minute/milliliter (mL)(for subjects with 2 known birth parents of at least 50% Japanese, Chinese, or Korean ancestry)

• History of asthma, anaphylaxis or anaphalactoid reactions, severe allergic responses

• History of hypercoagulable state or history of thrombosis

• A history of biliary tract disease including a history of liver disease with elevated liver function tests of known or unknown etiology

• Positive Human immunodeficiency virus (HIV), Hepatitis B or Hepatitis C at screening

• History of regular use of tobacco- or nicotine-containing products within three months of the study and/or has a positive breath CO at screening

• History of alcohol consumption exceeding, on average, 21 drinks/week for men (1 drink = 100 mL of wine or 240 mL of beer or 30 mL of hard liquor in Australia) within 6 months of the first dose of study medication

• Positive urine drug or positive breath alcohol test at screening or at admission to Clinical Research Unit

• Unable to refrain from use of prescription or non-prescription drugs and vitamins within 7 days or 5 half-lives (whichever is longer) prior to administration of study

• Unable to refrain from use of dietary/herbal supplements including (but not limited to) St. John's wort, kava, ephedra (ma huang), gingko biloba, DHEA, yohimbe, saw palmetto, ginseng and red yeast rice within 14 days prior to treatment with study medication

• Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing

• Unable to refrain from consumption of grapefruit or grapefruit juice within 7 days prior to the first dose of study medication

• For male subjects, an unwillingness to abstain from sexual intercourse with pregnant or lactating women or an unwillingness to use a condom plus partner use of a highly effective contraceptive if engaging in sexual intercourse with a woman who could become pregnant until discharge from the study

• Donation of blood in excess of 500 mL within 56 days prior to dosing

• History of sensitivity to heparin or heparin-induced thrombocytopenia

• Subjects, who in the investigator's judgement, pose a significant suicide risk. Evidence of serious suicide risk may include any history of suicidal behaviour and/or any suicidal ideation of type 4 or 5 on the C-SSRS in the last 6 months

Related Conditions & MeSH terms

• Alzheimer Disease
• Alzheimer's Disease

Intervention

Drug:
• GSK2647544
Capsules containing 0.5mg to 50mg of GSK2647544.
• Placebo
Matching placebo capsules.

Locations

Country	Name	City	State
Australia	GSK Investigational Site	Randwick	New South Wales

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and tolerability of GSK2647544 as assessed by number of subjects with adverse events (AE)s	Safety and tolerability parameters will include recording of AEs	5 days in each of the 4 dosing session
Primary	Safety and tolerability of GSK2647544 as assessed by change from Baseline in laboratory values	Safety and tolerability parameters will include laboratory (haematology, clinical chemistry, urinalysis) values at Screening, Day -1, Day 3 and Follow-up (7-14 days post-last dose)	5 days in each of the 4 dosing session
Primary	Safety and tolerability of GSK2647544 as assessed by change from Baseline in ECG readings	Safety and tolerability parameter will include the electrocardiogram (ECG) readings at Screening, Day -1, Day 1, Day 2, Day 3 and Follow-up (7-14 days post-last dose)	5 days in each of the 4 dosing session
Primary	Safety and tolerability of GSK2647544 as assessed by change from Baseline in Telemetry ECG parameters	Safety and tolerability parameter will include the Telemetry ECG readings from 30 minutes pre-dosing till 48 hours post-dosing	3 Days in each of the 4 dosing session
Primary	Safety and tolerability of GSK2647544 as assessed by change from Baseline in vital signs	Vital signs measurement include systolic and diastolic blood pressure and pulse rate at Screening, Day -1, Day 1, Day 2, Day 3, Day 4 and Follow-up (7-14 days post-last dose)	5 days in each of the 4 dosing session
Primary	Safety and tolerability of GSK2647544 as assessed by using the Columbia Suicide Severity Rating Scale (C-SSRS)	C-SSRS will be measured at Screening, Day -1, Day 1 (conducted prior to discharge) and Follow-up (7-14 days post-last dose)	5 days in each of the 4 dosing session
Secondary	Peak plasma concentration (Cmax) of GSK2647544	To assess PK profile of GSK2647544, Cmax of GSK2647544 will be measured	4 Days in each of the 4 dosing session
Secondary	Time of peak plasma concentration (tmax) of GSK2647544	To assess PK profile of GSK2647544 tmax of GSK2647544 will be measured	4 Days in each of the 4 dosing session
Secondary	Area under the time concentration curve (AUC) of GSK2647544	To assess PK profile of GSK2647544 AUC of GSK2647544 will be measured	4 Days in each of the 4 dosing session
Secondary	Terminal half-life (t½ ) of GSK2647544	To assess PK profile of GSK2647544 t½ of GSK2647544 will be measured	4 Days in each of the 4 dosing session
Secondary	Apparent oral clearance (CL/F) of GSK2647544	To assess PK profile of GSK2647544 CL/F of GSK2647544 will be measured	4 Days in each of the 4 dosing session
Secondary	Predose plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) activity and postdose Lp-PLA2 activity	It will be measured at Day 1, Day 2, Day 3, Day 4 and Day 5	5 Days in each of the 4 dosing session

External Links

•   Results for study 116698 can be found on the GSK Clinical Study Register.