A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Oral and Intravenous GSK1322322 in Healthy Subjects

Infections, Bacterial Clinical Trial

Official title:

A Randomized, Double-Blind, Placebo-Controlled Repeat Dose Escalation, First Time in Human Study to Investigate the Safety, Tolerability and Pharmacokinetics of Oral and Intravenous GSK1322322 in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01610388
• Other study ID #: 113376
• Status: Completed
• Phase: Phase 1
• First received: May 31, 2012
• Last updated: June 9, 2017
• Start date: September 13, 2011
• Est. completion date: January 26, 2012

Study information

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

Clinical Trial Summary

This first time in human (FTIH) study will be the first administration of GSK1322322 as an intravenous formulation and will investigate safety, tolerability, and pharmacokinetics in healthy subjects. One cohort of subjects will undergo bronchoalveolar lavage (BAL) for determination of GSK1322322 concentrations in lung with simultaneous comparison to plasma concentrations to evaluate drug penetration in the lung. The study will evaluate the absolute bioavailability of an oral tablet formulation as compared to the IV formulation.In addition, Amendment 01 will enable the investigation of an improved IV formulation (GSK1322322J mesylate salt) in an additional repeat dosing cohort and the supra-therapeutic cohort.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: January 26, 2012
• Est. primary completion date: January 26, 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Healthy as determined by a responsible and experienced physician, based on a medical evaluation including [medical history, physical examination, laboratory tests and ECGs. A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included at the discretion of the Investigator only if the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.

• Male or female between 18 and 65 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

• Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods listed in the protocol. This criterion must be followed from the time of the first dose of study medication until the final follow up visit.

• Body weight greater than or equal to 50 kilograms and body mass index (BMI) between 18.5-29.9 (inclusive).

• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

• QTcB less than 450 millisecond (msec); or QTcB less than 480 msec in subjects with Bundle Branch Block on Screening ECG

Exclusion Criteria:

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening

• Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).

• Contraindications to bronchoalveolar lavage including hypercapnia greater than 50 mm Hg, refractory hypoxemia, reactive airway disease or asthma, unstable angina or acute myocardial infarction in the last 6 months, heart failure, and severe hemostatic alterations (Cohort C only).

• A positive pre-study drug/alcohol screen.

• A positive test for 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 the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).

• 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 (including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, and within 5 days following discontinuation of GSK1322322 (for sensitive and narrow therapeutic index CYP3A4 substrates), unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.

• Use of antacids, H2 blockers, proton pump inhibitors, vitamins, and iron supplements within 7 days prior to the first dose of study medication and for the duration of the trial, including follow-up.

• 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 medications used in study, ie Atropine, Midazolam, Fentanyl, Lidocaine, Codeine (Cohort C only) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.

• Where participation in the study would result in donation of blood or blood products in excess of 500 milliliters within a 56 day period.

• Pregnant females as determined by positive [serum or urine] test at screening or prior to dosing.

Lactating females.

• Unwillingness or inability to follow the procedures outlined in the protocol.

• Subject is mentally or legally incapacitated.

• History of sensitivity to heparin or heparin-induced thrombocytopenia.

• Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.

• Consumption of red wine, seville oranges, grapefruit or grapefruit juice [and/or pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices] from 7 days prior to the first dose of study medication.

• Exclusion criteria for screening ECG (a single repeat is allowed for eligibility determination): Heart rate: males less than 45 and greater than 100 beats per minute (bpm) and females less than 50 and greater than 100bpm. PR interval less than 120 and greater than 220msec, QRS duration less than 70 and greater than 120 msec, and QTcB greater than 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, AV block [2nd degree or higher], Wolf Parkinson White [WPW] syndrome), sinus pauses> 3 seconds, non-sustained or sustained ventricular tachycardia (greater than or equal to 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.

Related Conditions & MeSH terms

• Bacterial Infections
• Infections, Bacterial

Intervention

Drug:
• 500mg IV GSK1322322/placebo
500mg IV
• 1000mg oral GSK1322322/placebo
1000mg oral
• 1000mg IV GSK1322322/placebo
1000mg IV
• 1500mg oral GSK1322322/placebo dose
1500mg oral
• 1500mg IV GSK1322322/placebo
1500mg IV
• 2000mg IV GSK1322322J/placebo
2000mg IV
• 3000mg IV GSK1322322J/placebo
3000mg IV
• 1000mg IV GSK1322322J/placebo
1000mg IV

Locations

Country	Name	City	State
United States	GSK Investigational Site	Minneapolis	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	GSK1322322 safety parameters including the number of subjects with adverse events (AEs)		Cohort A up to 14 days; Cohort B and C up to 16 days
Primary	GSK1322322 safety parameters including absolute values and changes over time of clinical safety laboratory assessments.		Cohort A up to 14 days; Cohort B and C up to 16 days
Primary	GSK1322322 safety parameters including the change from baseline in vital signs (blood pressure (BP) and heart rate)		Cohort A up to 14 days; Cohort B and C up to 16 days
Primary	GSK1322322 safety parameters including change from baseline in electrocardiogram (ECG) parameters		Cohort A up to 14 days; Cohort B and C up to 16 days
Primary	GSK1322322 pharmacokinetic parameters (PK) after single oral dose, area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC(0-t)).		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC(0-8)).		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose aximum observed concentration (Cmax).		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose time of occurrence of Cmax (tmax).		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose mean residence time (MRTpo)		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose apparent clearance after oral administration (CL/F)		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose apparent volume of distribution after oral administration (Vz/F)		Cohorts B and C on Day -2
Primary	GSK1322322 PK parameters after single oral dose terminal phase half-life (t 1/2).		cohort B and C on Day -2
Primary	GSK1322322 PK parameters after single IV dose area under the concentration-time curve from zero (pre-dose) to some fixed nominal time (12 hours) (AUC(0-12)).		Cohorts A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose area under the concentration-time curve from zero (pre-dose) to some fixed nominal time (24 hours) AUC(0-24)		Cohorts A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose AUC(0-t)		Cohorts A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose AUC(0-8).		Cohorts A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose Cmax		Cohorts A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose mean residence time intravenous (MRTiv)		Cohort A, B, C, D, E on Day 1
Primary	GSK1322322 PK parameters after single IV dose t1/2		Cohort A, B, C, D, E on Day 1
Primary	Absolute bioavailability will be determined by comparing oral AUC(0-8) to IV AUC(0-8)		Cohort B and C on Day -2 and Day 1
Primary	MAT of oral tablet will be determined (=MRTpo-MRTiv)		Cohort B and C on Day -2 and Day 1
Primary	After repeated IV doses, pharmacokinetic parameters including Area under the concentration-time curve over the dosing interval (AUC(0-t))		Cohorts A, B, C on Days 3 - 6
Primary	After repeated IV doses, pharmacokinetic parameters including Cmax		Cohorts A, B, C on Days 3 - 6
Primary	After repeated IV doses, pharmacokinetic parameters including CL		Cohorts A, B, C on Days 3 - 6
Primary	GSK1322322 concentrations in BAL obtained in epithelial lining fluid (ELF) and alveolar macrophages (AM) as compared to that in plasma		Cohort C Day 6
Secondary	GSK1322322 urine PK parameters: amount excreted (Ae) of unchanged GSK1322322, fraction of the dose excreted in the urine (fe) and renal clearance (CLr) following single dose IV administration from Period 2 and Period 3.		cohort B and C on Day 1 and 2
Secondary	Day 6 GSK1322322 AUC(0-t) compared to AUC(0-12) on Day 1 to evaluate the accumulation ratio following repeat IV administration of GSK1322322.		Cohorts A, B, C Day 6 and Day 1
Secondary	Day 6 GSK1322322 AUC(0-t) compared to AUC(0-8) on Day 1 to evaluate time invariance following repeat IV administration of GSK1322322.		Cohorts A, B, C Day 6 and Day 1
Secondary	GSK1322322 PK parameters: AUC(0-8) on Day 1 and AUC(0-t) on Day 6 following IV administration at different doses for the assessment of dose proportionality.		Cohorts A, B, C Day1 and 6
Secondary	Microbiome analysis of stool prior to and after exposure to GSK1322322		Cohort A, B,C, D, E single sample predose and single sample post dose
Secondary	GSK1322322J safety parameters including the number of subjects with adverse events (AEs)		Cohort D and E up to 11 days, Cohort F up to 14 days
Secondary	GSK1322322J safety parameters including absolute values and changes over time of clinical safety laboratory assessments		Cohort D and E up to 11 days; Cohort F up to 14 days
Secondary	GSK1322322J safety parameters including the change from baseline in vital signs (blood pressure (BP) and heart rate)		Cohort D and E up to 11 days; Cohort F up to 14 days
Secondary	GSK1322322J safety parameters including change from baseline in electrocardiogram (ECG) parameters		Cohort D and E up to 11 days: Cohort F up to 14 days

External 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.
•   Results for study 113376 can be found on the GSK Clinical Study Register.