A Study to Evaluate the Pharmacokinetics (PK), Safety and Tolerability, Immunogenicity, and Pharmacodynamics (PD) of GSK2800528 in Healthy Subjects.

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ClinicalTrials.gov Identifier: NCT01899755

Recruitment Status : Completed

First Posted : July 15, 2013

Last Update Posted : May 11, 2017

View this study on Beta.ClinicalTrials.gov

Sponsor:

Information provided by (Responsible Party):

GlaxoSmithKline

Study Description

Brief Summary:

GSK2800528 is being developed as a human anti-tumor necrosis factor (TNF) alpha monoclonal antibody (mAb) for the treatment of immune-inflammatory diseases. The study will be conducted in healthy volunteers and divided into 4 cohorts. Cohorts 1 to 3 will consist of groups of 12 subjects, 9 on active treatment (GSK2800528), and 3 on placebo. Cohort 4 will consist of a group of 9 subjects, all on active treatment (adalimumab).

Condition or disease	Intervention/treatment	Phase
Psoriasis	Drug: GSK2800528, solution for injection Drug: Placebo (0.9% w/v Sodium Chloride), solution for injection Drug: Adalimumab, solution for injection	Phase 1

Study Design

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Study Type :	Interventional (Clinical Trial)
Actual Enrollment :	45 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Masking:	Double (Participant, Investigator)
Primary Purpose:	Treatment
Official Title:	A Study to Evaluate the Pharmacokinetics, Safety and Tolerability, Immunogenicity, and Pharmacodynamics of GSK2800528 in Healthy Subjects.
Actual Study Start Date :	July 10, 2013
Actual Primary Completion Date :	April 3, 2014
Actual Study Completion Date :	April 3, 2014

Resource links provided by the National Library of Medicine

Drug Information available for: Adalimumab

U.S. FDA Resources

Arms and Interventions

Arm	Intervention/treatment
Experimental: GSK2800528 Arm Subjects will be assigned to treatments in accordance with the randomization schedule in Cohorts 1 to 3. Treatments will be randomized with placebo in a 3:1 ratio. The final randomization code will also pre-define the sentinel subjects to ensure that of the first two subjects in each cohort, one will receive GSK2800528 and the other will receive placebo.	Drug: GSK2800528, solution for injection Drug will be administered at 3 different dose levels by subcutaneous injection.
Placebo Comparator: Placebo Arm Subjects will be assigned to treatments in accordance with the randomization schedule in Cohorts 1 to 3. Treatments will be randomized with placebo in a 3:1 ratio. The final randomization code will also pre-define the sentinel subjects to ensure that of the first two subjects in each cohort, one will receive GSK2800528 and the other will receive placebo.	Drug: Placebo (0.9% w/v Sodium Chloride), solution for injection Subcutaneous injection of. 0.8 mL solution will be administered
Active Comparator: Adalimumab Arm In Cohort 4, all subjects will receive adalimumab 40 mg (0.8 mL solution) as subcutaneous injection	Drug: Adalimumab, solution for injection Subcutaneous injection of 0.8 mL solution will be administered (40mg)

Outcome Measures

Primary Outcome Measures :

Apparent systemic clearance (CL/F) of GSK2800528 [ Time Frame: Up to Day 196 ]
Apparent systemic clearance (CL/F) of adalimumab [ Time Frame: Up to Day 140 ]
Adverse event (AE) and Serious Adverse event (SAE) reporting [ Time Frame: Up to Day 196 ]
An AE is any untoward medical occurrence in a patient or clinical investigation subject, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An SAE is any untoward medical occurrence that, at any dose: results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect, is associated with liver injury and impaired liver function.
Laboratory safety assessment for clinical chemistry parameters [ Time Frame: Up to Day 196 ]
Safety data for laboratory clinical chemistry parameters including albumin, creatinine, glucose, sodium, potassium, chloride, calcium, total protein, aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma glutamyl transferase (GGT), alkaline phosphatise, total and direct bilirubin, and uric acid will be assessed
Laboratory safety assessment for hematology parameters [ Time Frame: Up to Day 196 ]
Safety data for laboratory hematology parameters including platelet count, red blood cell (RBC) count, absolute white blood cell (WBC) count, reticulocyte count, hemoglobin, hematocrit, mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC), mean corpuscular haemoglobin (MCH), neutrophils, lymphocytes, monocytes, eosinophils, and basophils will be assessed.
Laboratory safety assessment for urinalysis parameters [ Time Frame: Up to Day 196 ]
Safety data for laboratory urinalysis parameters including specific gravity, pH, glucose, protein, blood and ketones by dipstick , and microscopic examination will be assessed
Vital signs monitoring (blood pressure, heart rate, body temperature) [ Time Frame: Up to Day 196 ]
Safety data for vital signs including blood pressure, heart rate, and body temperature will be measured
Electrocardiogram (ECG) monitoring [ Time Frame: Up to Day 196 ]
Supine 12-lead ECG data will be monitored

Secondary Outcome Measures :

Plasma concentrations of GSK2800528 and derived pharmacokinetic parameters other than CL/F [ Time Frame: Up to Day 196 ]
Blood samples for PK analysis of GSK2800528 will be collected to assess plasma concentration and derived PK parameters including maximum observed plasma concentration (Cmax), time to Cmax (tmax), area under the plasma concentration time curve [AUC(0-t) and AUC(0-infinity)], and apparent terminal phase half-life (t1/2)
Plasma concentrations of adalimumab and derived pharmacokinetic parameters other than CL/F [ Time Frame: Up to Day 140 ]
Blood samples for PK analysis of adalimumab will be collected to assess plasma concentration and derived PK parameters including Cmax, tmax, AUC(0-t) and AUC(0-infinity), and t1/2
Incidence, titers, and specificity of anti-GSK2800528 antibodies. [ Time Frame: Up to Day 196 ]
Incidence, titers, and specificity of anti-adalimumab antibodies [ Time Frame: Up to Day 140 ]
Neutralising activity for samples with confirmed anti-drug antibodies [ Time Frame: Up to Day 196 ]

Eligibility Criteria

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Ages Eligible for Study:	18 Years to 65 Years (Adult, Older Adult)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	Yes

Criteria

Inclusion Criteria:

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%).
Average bazett's corrected QT interval (QTcB) < 450 msec, or QTcB < 480 msec in subjects with Bundle Branch Block.
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 at the investigator's discretion provided the finding is unlikely to introduce additional risk factors, jeopardize study integrity, or to 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 [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) > 21.7 international unit/liter (IU/L) and oestradiol <110 picomoles/liter (pmol/L) is confirmatory. Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods specified in study protocol.
Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods specified in study protocol.
Body weight >= 60 kg and body mass index (BMI) within the range 19 to 31 kilogram/meter2 (kg/m2) (inclusive).

Exclusion Criteria:

A positive pre-study Quantiferon test, Hepatitis B surface antigen, or positive Hepatitis C antibody result within 3 months of screening.
Current or chronic history of liver or kidney disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
A positive pre-study drug/alcohol screen.
A positive test for human immunodeficiency virus (HIV) antibody.
Previous treatment with adalimumab.
Current, or history of, cancer.
History of regular alcohol consumption within 6 months of the study defined as: an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (~240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.
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: 3 months, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
Travel to regions of high endemic tuberculosis/infection, as judged by the investigator or medical monitor, is prohibited from the start of screening until the final follow up visit.
Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
Unable to refrain from the 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, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
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.
Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
Unwillingness or inability to follow the procedures outlined in the protocol.
Subject is mentally or legally incapacitated.
Current evidence or history of bacterial, viral, or fungal infection within 7 days before dosing.
Subject has received any type of vaccination within 21 days before dosing or will require vaccination prior to the end of the study.

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01899755

Locations

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United Kingdom
GSK Investigational Site
London, United Kingdom, NW10 7EW

Sponsors and Collaborators

GlaxoSmithKline

Investigators

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Study Director:	GSK Clinical Trials	GlaxoSmithKline

More Information

Additional Information:

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