This Study Will Investigate the Safety, Tolerability and Pharmacokinetic Profile of Repeat Oral Doses of GSK2140944 in Healthy Adult Subjects

A Randomized, Single Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Repeat Escalating Oral Doses of GSK2140944 in Healthy Adult Subjects (BTZ116778)

This will be a randomized, placebo-controlled, single blind study to investigate the safety, tolerability and pharmacokinetic (PK) profile of GSK2140944 following repeat oral doses in healthy adult subjects. The study will include a Screening period (40 days), Treatment period (16 days) and a Follow-up period (26 to 30 days). A single dose will be administered on Day 1 for characterization of single dose PK, followed by twice-daily (BID) or thrice-daily (TID) dosing on Days 3 to 16. Subjects may only be randomized to one cohort per the randomization schedule. Up to 6 cohorts will be enrolled using a sequential panel. Subjects in Cohort 1 will receive GSK2140944 (6) and placebo (2). Subsequent cohorts will enroll 16 subjects such that 12 subjects will receive GSK2140944 and 4 subjects will receive placebo, per dose level according to the randomization schedule. Dose escalations are planned to run in successive weeks. Cohort 2 may begin dosing once subjects in Cohort 1 have completed 7 days of BID dosing, PK data is reviewed and safety data from at least 6 subjects is available. Each subsequent dose escalation will commence only when GSK2140944 safety data and available PK data of at least 12 subjects dosed at the previous dose level have been reviewed. The number of cohorts may be reduced or expanded if needed. The first planned dose is 400 milligram (mg) BID but may be modified based upon emergent PK, safety and tolerability data from ongoing clinical study BTZ115198 evaluating single and repeat intravenous (IV) doses of GSK2140944. The projected dose for Cohort 2 is 800 mg BID, Cohort 3 is 1500 mg BID, Cohort 4 is 2300 mg BID or 1500 mg TID and Cohort 5 and cohort 6 will be decided later. The planned maximum dose is 2500 mg TID but may be modified based upon emergent safety, tolerability and PK data. Doses of GSK2140944 or placebo will be administered following a moderate fat meal.

Study Overview

• Status: Completed
• Conditions: Infections, Respiratory Tract
• Intervention / Treatment: Drug: Placebo; Drug: GSK2140944

• Study Type: Interventional
• Enrollment (Actual): 72
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Kansas
    • Overland Park, Kansas, United States, 66211
      • GSK Investigational Site

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 60 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase and bilirubin <=1.5x upper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
• Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. - A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator and the GlaxSmithKline (GSK) Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
• Male or female between 18 and 60 years of age inclusive, at the time of signing the informed consent.
• 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 defined as 12 months of spontaneous amenorrhea. To confirm post-menopausal status, a blood sample for simultaneous follicle stimulating hormone (FSH) >40 MlU/ml and estradiol <40 pg/ml (<147 pmol/L) is confirmatory. Male subjects with female partners of child-bearing potential must agree to use the contraception methods. This criterion must be followed from the time of the first dose of study medication until the final follow-up visit.
• Body weight >=50 kg and body mass index (BMI) within the range 19 to 31 kg/m2 (inclusive).
• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion Criteria:

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening or positive Human Immunodeficiency Virus (HIV) antibody.
• Current or chronic history of liver disease, or known hepatic or biliary abnormalities.
• Any clinically significant central nervous system (e.g., seizures), cardiac, pulmonary, metabolic, renal, hepatic or gastrointestinal conditions or history of such conditions that, in the opinion of the investigator may place the subject at an unacceptable risk as a participant in this trial or may interfere with the absorption, distribution, metabolism or excretion of drugs.
• A screening or Day -2 urinalysis positive for protein or glucose (greater than "trace" findings of protein or glucose).
• A serum creatinine value between screening and Day -2 visit that is increased by more than 0.2 mg/dL (or 15.25 umol/L) changes.
• History of photosensitivity to quinolones and tendon rupture.
• Unwillingness to commit to avoid excessive exposure to sunlight which would cause a sunburn reaction from first dose up to and including the follow-up visit.
• A positive urine test for drugs of abuse or alcohol (or alcohol breath test) at screening or Day -2.
• History of drug abuse within 6 months of the study
• History of smoking or use of nicotine containing products within 3 months of screening, or a positive urine cotinine indicative of smoking at screening.
• History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >14 drinks for males or >7 drinks for females. One drink is equivalent to 12 g of alcohol: 12 ounces (360 ml) of beer, 5 ounces (150 ml) of wine or 1.5 ounces (45 ml) of 80 proof distilled spirits.
• The subject has participated in a clinical trial and has received a drug or a new chemical entity within 30 days or 5 half-lives, or twice the duration of the biological effect of any drug (whichever is longer) prior to the first dose of current study medication.
• Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study medication, or use of St. John's Wort within 14 days prior to the first dose of study medication. By exception, the volunteer may take paracetamol or acetaminophen (<=2 grams/day) up to 48 hours prior to the first dose of study medication. However, the Investigator and GSK study team can review medication on a case by case basis to determine if its use would compromise subject safety or interfere with the study procedures or data interpretation.
• 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 GSK Medical Monitor, contraindicates their participation.
• History of sensitivity to heparin or heparin-induced thrombocytopenia (if the clinical research unit uses heparin to maintain intravenous cannula patency).
• Donation of blood in excess of 500 ml within 12 weeks prior to dosing.
• Consumption of red wine, seville oranges, grapefruit or grapefruit juice, pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices containing such products from 7 days prior to the first dose of study medication.
• Screening ECG: Heart rate <40 and >100 bpm for males and <50 and >100 bpm for females. PR Interval <120 and >220 msec, QRS duration <70 and >100 msec, QTcB or QTcF interval >450msec. Evidence of previous myocardial infarction (does not include ST segment changes associated with repolarization); any conduction abnormality (including but not specific to left or right complete bundle branch block, atrioventricular (AV) block [2nd degree or higher], Wolf Parkinson White [WPW] syndrome), sinus pauses >3 seconds, non-sustained or sustained ventricular tachycardia (>=3 consecutive ventricular ectopic beats) or any significant arrhythmia which, in the opinion of the principal investigator and GSK medical monitor, will interfere with the safety of the individual subject.
• Screening holter monitoring shows one or more of the following: any symptomatic arrhythmia (except isolated extra systoles); sustained cardiac arrhythmias (such as atrial fibrillation or flutter, supraventricular tachycardia (SVT) [>10 consecutive beats]); sinus tachycardia (or SVT) >150 bpm; non-sustained or sustained ventricular tachycardia (defined as >=3 consecutive ventricular ectopic beats); any conduction abnormality (including but not specific to left or right complete bundle branch block, AV block [2nd degree or higher in an awake subject], WPW syndrome, other pre-excitation syndromes); symptomatic sinus pause or sinus pause >3 seconds - unless patient is straining, vomiting, or having some other type of hypervagal response; 300 or more supraventricular ectopic beats in 24 hours; 250 or more ventricular ectopic beats in 24 hours; Ischemia, diagnosed by a sequence of EKG changes that include flat or down sloping ST-segment depression >0.1 mV, with a gradual onset and offset that lasts for a minimum period of 1 minute. Each episode of ischemia must be separated by a minimum duration of at least 1 minute, during which the ST segment returns back to baseline (1x1x1 rule).
• Unwillingness or inability to follow the procedures outlined in the protocol.
• Subject is mentally or legally incapacitated.
• Neutrophil count <2000 cells per microliter (a single repeat is allowed for eligibility determination).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

12

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Cohort 1 - GSK2140944 400 mg; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 1 - Placebo; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 BID or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available
Experimental: Cohort 2 - GSK2140944 800 mg; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 2 will be decided based on the safety and PK data from six subjects in Cohort 1	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 2 - Placebo; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 BID or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available
Experimental: Cohort 3 - GSK2140944 1500 mg; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 3 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 2	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 3 - Placebo; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 bid or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available
Experimental: Cohort 4 - GSK2140944 2500 mg; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 4 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 3	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 4 - Placebo; Subjects will be randomized in 12:4 ratio to receive either GSK2140944 bid or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available
Experimental: Cohort 5 - GSK2140944 TBD; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) TID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 5 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 4	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 5 - Placebo; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 TID or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available
Experimental: Cohort 6 - GSK2140944 TBD; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) TID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 5 will be decided on the safety data and available PK data from at least 6 subjects dosed at the Cohort 5	Drug: GSK2140944; GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg
Placebo Comparator: Cohort 6 - Placebo; Subjects will be randomized in 6:2 ratio to receive either GSK2140944 TID or matching placebo for approximately 15 days	Drug: Placebo; Matching placebo will be available

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
GSK2140944 clinical safety data assessed as change from baseline in 12-lead ECG	12-lead ECGs will be obtained at each timepoint using an ECG machine, after the subject has rested in a semi-supine position for at least 10 minutes	Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and at the Follow-up visit
GSK2140944 clinical safety data from dual-lead cardiac monitoring	Continuous dual-lead cardiac monitoring will be obtained at each timepoints using an ECG machine	Day 1
GSK2140944 clinical safety data assessed as change from baseline in clinical laboratory tests	Clinical laboratory assessments will include hematology, clinical chemistry, routine urinalysis and additional parameters	Day -2 and pre-morning dose on Day 2, Day 5, Day 8, Day 11, and Day 14; on the morning of Day 17 and at the Follow-up visit
GSK2140944 clinical safety data assessed as by number of adverse events (AE)	Safety and tolerability parameters will include recording of AEs, throughout the study	Up to the Follow-up visit
GSK2140944 clinical safety data assessed as change from baseline in blood pressure	Vital sign measurements will be done in semi-supine position and will include systolic and diastolic blood pressure	Day -1, Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and the Follow-up visit
GSK2140944 clinical safety data assessed as change from baseline in heart rate	Vital sign measurements will be done in semi-supine position and will include pulse rate	Day -1, Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and the Follow-up visit
Pharmacokinetic parameter: AUC(0-12) following single dose of GSK2140944	Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 12 hour post-dose (AUC(0-12)) following single dose of GSK2140944	Day 1
Pharmacokinetic parameter: AUC(0-24) following single dose of GSK2140944	Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 24 hour post-dose (AUC(0-24)) following single dose of GSK2140944	Up to Day 2
Pharmacokinetic parameter: AUC(0-t) following single dose of GSK2140944	Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC(0-t)) following single dose of GSK2140944	Up to Day 3
Pharmacokinetic parameter: AUC(0-infinity) following single dose of GSK2140944	Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC(0-infinity)) following single dose of GSK2140944	Up to Day 3
Pharmacokinetic parameter: Cmax following single dose of GSK2140944	Pharmacokinetic data will include maximum observed concentration (Cmax) following single dose of GSK2140944	Up to Day 3
Pharmacokinetic parameter: tmax following single dose of GSK2140944	Pharmacokinetic data will include time of occurrence of Cmax (tmax) following single dose of GSK2140944	Up to Day 3
Pharmacokinetic parameter: t1/2 following single dose of GSK2140944	Pharmacokinetic data will include terminal phase half-life (t1/2) following single dose of GSK2140944	Up to Day 3
Pharmacokinetic parameter: AUC(0-tau) following repeat dose of GSK2140944	Pharmacokinetic data will include area under the concentration-time curve over the dosing interval (AUC(0-tau)) following repeat dose of GSK2140944	Day 14, Day 15 and Day 16
Pharmacokinetic parameter: Cmax following repeat dose of GSK2140944	Pharmacokinetic data will include Cmax following repeat dose of GSK2140944	Day 14, Day 15 and Day 16
Pharmacokinetic parameter: tmax following repeat dose of GSK2140944	Pharmacokinetic data will include tmax following repeat dose of GSK2140944	Day 14, Day 15 and Day 16
Pharmacokinetic parameter: Ctau following repeat dose of GSK2140944	Pharmacokinetic data will include pre-dose (trough) concentration at the end of the dosing interval (Ctau) following repeat dose of GSK2140944	Day 14, Day 15 and Day 16
Pharmacokinetic parameter: Ro following repeat dose of GSK2140944	Pharmacokinetic data will include accumulation ratio (Ro) following repeat dose of GSK2140944	Day 14, Day 15 and Day 16
Pharmacokinetic parameter: AUC(0-8) following single dose of GSK2140944	Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 8 hour post-dose (AUC[0-8]) following single dose of GSK2140944	Day 1

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
To assess preliminary dose proportionality using PK parameter AUC(0-infinity) following single dose of GSK2140944	Preliminary dose proportionality will be assessed using PK parameter (AUC(0-infinity)) following single dose of GSK2140944	Up to Day 3
To assess preliminary dose proportionality using PK parameter Cmax following single dose of GSK2140944	Preliminary dose proportionality will be assessed using PK parameter Cmax following single dose of GSK2140944	Up to Day 3
To assess preliminary dose proportionality using PK parameter AUC(0-tau) following repeat doses of GSK2140944	Preliminary dose proportionality will be assessed using PK parameter (AUC(0-tau) following repeat doses of GSK2140944	Day 14, Day 15 and Day 16
To assess preliminary dose proportionality using PK parameter Cmax following repeat doses of GSK2140944	Preliminary dose proportionality will be assessed using PK parameter Cmax following repeat doses of GSK2140944	Day 14, Day 15 and Day 16
To examine extent of accumulation using PK parameter Ro using AUC(0-tau) following repeat doses of GSK2140944	Accumulation ratio will be assessed using PK parameter AUC(0-tau) following repeat doses of GSK2140944	Day 14, Day 15 and Day 16
To examine extent of accumulation using PK parameter AUC(0-tau) following single dose of GSK2140944	Accumulation ratio will be assessed using PK parameter AUC(0-tau) following single dose of GSK2140944	Day 1
To examine the extent of time invariance using repeat dose AUC(0-tau)	The extent of time invariance will be assessed using PK parameter AUC(0-tau) following repeat dose	Day 14, Day 15 and Day 16
To examine the extent of time invariance using single dose AUC(0-infinity)	The extent of time invariance will be assessed using PK parameter AUC(0-infinity) following single dose	Up to Day 3
To assess achievement of steady-state following repeat oral doses of GSK2140944	Achievement of steady-state will be assessed using trough concentrations at the end of the dosing interval (Ctau) collected at pre-morning dose on Days 14 and 15 (together with pre-morning dose Ctau on Days 16 from the full PK profiles on Day 16).	Day 14, Day 15 and Day 16

Collaborators and Investigators

• Sponsor: GlaxoSmithKline

Publications and helpful links

Helpful Links

• Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.

Study record dates

Study Major Dates

• Study Start (Actual): October 17, 2012
• Primary Completion (Actual): December 13, 2013
• Study Completion (Actual): December 13, 2013

Study Registration Dates

• First Submitted: October 11, 2012
• First Submitted That Met QC Criteria: October 11, 2012
• First Posted (Estimate): October 15, 2012

Study Record Updates

• Last Update Posted (Actual): May 9, 2017
• Last Update Submitted That Met QC Criteria: May 5, 2017
• Last Verified: May 1, 2017

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Infections; Respiratory Tract Diseases; Respiratory Tract Infections
• Other Study ID Numbers: 116778

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Study Data/Documents

1. Informed Consent Form
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
2. Individual Participant Data Set
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
3. Clinical Study Report
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
4. Study Protocol
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
5. Annotated Case Report Form
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
6. Statistical Analysis Plan
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register
7. Dataset Specification
   Information identifier: 116778
   Information comments: For additional information about this study please refer to the GSK Clinical Study Register