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A Phase I Rheumatoid Arthritis Study in Healthy Volunteers

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00539760
First Posted: October 5, 2007
Last Update Posted: August 15, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
GlaxoSmithKline
October 4, 2007
October 5, 2007
August 15, 2017
September 5, 2007
April 5, 2008   (Final data collection date for primary outcome measure)
  • Number of subjects with abnormal clinical chemistry findings [ Time Frame: Up to 29 days ]
    Blood samples will be collected at specific time points as a measure of safety
  • Number of subjects with abnormal clinical hematology findings [ Time Frame: Up to 29 days ]
    Blood samples will be collected at specific time points as a measure of safety
  • Number of subjects with abnormal urinalysis findings [ Time Frame: Up to 29 days ]
    Urine samples will be collected at specific time points as a measure of safety
  • Number of subjects with abnormal blood pressure values [ Time Frame: Up to 29 days ]
    Systolic and diastolic blood pressure will be measured in a supine position after at least 5 minutes of rest as a measure of safety.
  • Number of subjects with abnormal heart rate values [ Time Frame: Up to 29 days ]
    Heart rate will be measured in a supine position after at least 5 minutes of rest as a measure of safety.
  • Number of subjects with abnormal respiratory rate values [ Time Frame: Up to 29 days ]
    Respiratory rate will be measured in a supine position after at least 5 minutes of rest as a measure of safety.
  • Number of subjects with abnormal body temperature findings [ Time Frame: Up to 29 days ]
    Body temperature will be measured in a supine position after at least 5 minutes of rest as a measure of safety.
  • Number of subjects with abnormal electrocardiogram (ECG) findings [ Time Frame: Up to 29 days ]
    12-lead ECG measurements will be performed in a supine position after at least 5 minutes of rest as a measure of safety
  • Number of subjects with adverse events (AEs) [ Time Frame: Up to 29 days ]
    An adverse event 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.
Safety and tolerability of GSK182771 at ascending doses monitoring will take place during the period the subjects are in-house (7 days) and when they come for the following visits (day 14, day 21, day 28 and follow-up if necessary) [ Time Frame: monitoring will take place during the period the subjects are in-house (7 days) and when they come for the following visits (day 14, day 21, day 28 and follow-up if necessary) ]
Complete list of historical versions of study NCT00539760 on ClinicalTrials.gov Archive Site
  • Plasma concentrations of GSK1827771 [ Time Frame: Pre-dose, 0.25, 0.5, 1, 2, 4, 8, 12, 24 hours post-dose on Day 1; in morning and evening on Day 2-7; in morning on Day 14, 21, 28 ]
    Blood samples will be collected at specific time points for calculating plasma concentrations of GSK1827771
  • Maximum plasma concentration (Cmax) of GSK1827771 [ Time Frame: Pre-dose, 0.25, 0.5, 1, 2, 4, 8, 12, 24 hours post-dose on Day 1; in morning and evening on Day 2-7; in morning on Day 14, 21, 28 ]
    Blood samples will be collected at specific time points for calculating Cmax of GSK1827771
  • Area under the curve (AUC) of GSK1827771 [ Time Frame: Pre-dose, 0.25, 0.5, 1, 2, 4, 8, 12, 24 hours post-dose on Day 1; in morning and evening on Day 2-7; in morning on Day 14, 21, 28 ]
    Blood samples will be collected at specific time points for calculating AUC of GSK1827771
  • Frequency of anti-GSK1827771 [ Time Frame: Up to 29 days ]
    The presence of anti-GSK1827771 binding antibodies will be assessed using an immunoelectrochemiluminescence screening assay (ECL).
  • Titer of anti-GSK1827771 [ Time Frame: Up to 29 days ]
    Blood samples for determination of anti-GSK1827771 antibodies will be taken at specific time points.
  • Frequency of anti-PEG [ Time Frame: Up to 29 days ]
    Antibodies to PEG components of GSK1827771 will be measured.
  • Titer of anti-PEG [ Time Frame: Up to 29 days ]
    Antibodies to PEG components of GSK1827771 will be measured.
  • Frequency of anti-dAb [ Time Frame: Up to 29 days ]
    Antibodies to dAb components of GSK1827771 will be measured.
  • Titer of anti-dAb [ Time Frame: Up to 29 days ]
    Antibodies to dAb components of GSK1827771 will be measured.
  • Change from Baseline response of whole blood to ex vivo stimulation with IL-1 alpha or IL-1 beta [ Time Frame: Baseline and up to 29 days ]
    Blood samples will be collected for assessment of pharmacodynamic activity of GSK1827771 at specific time points
  • Exploratory biomarker levels in blood [ Time Frame: Up to 29 days ]
    Blood samples will be taken for exploratory biomarker analysis
Pharmacokinetics, pharmacodynamics, immunogenicity of GSK1827771. monitoring will take place during the period the subjects are in-house (7 days) and when they come for the following visits (day 14, day 21, day 28 and follow-up if necessary) [ Time Frame: monitoring will take place during the period the subjects are in-house (7 days) and when they come for the following visits (day 14, day 21, day 28 and follow-up if necessary) ]
Not Provided
Not Provided
 
A Phase I Rheumatoid Arthritis Study in Healthy Volunteers
A Phase I, Randomized, Observer- and Subject-Blind, Placebo-Controlled, Single Ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of GSK1827771 in Healthy Volunteers
GSK182771 is a domain antibody targeting the interleukin (IL)-1 receptor which is being developed for the treatment of rheumatoid arthritis. This study is being done in healthy volunteers to verify the safety and tolerability of GSK182771
Not Provided
Interventional
Phase 1
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Arthritis, Rheumatoid
  • Drug: GSK1827771
    GSK1827771 will be administered using injection via subcutaneous (SC) route.
  • Drug: Placebo
    Placebo to GSK1827771 for Injection will be administered via SC route
  • Experimental: Subjects receiving GSK 1827771 in sub-cohort Xa (Cohort 1-5)
    Eligible subjects will receive GSK1827771 with the starting dose of 0.3 milligram (mg)
    Intervention: Drug: GSK1827771
  • Placebo Comparator: Subjects receiving placebo in sub-cohort Xa (Cohort 1-5)
    Eligible subjects will receive placebo matching to GSK1827771
    Intervention: Drug: Placebo
  • Experimental: Subjects receiving GSK 1827771 in sub-cohort Xb (Cohort 1-5)
    Eligible subjects will receive GSK1827771 via injection
    Intervention: Drug: GSK1827771
  • Placebo Comparator: Subjects receiving placebo in sub-cohort Xb (Cohort 1-5)
    Eligible subjects will receive placebo matching to GSK1827771
    Intervention: Drug: Placebo
  • Experimental: Subjects receiving GSK 1827771 in sub-cohort Xc (Cohort 1-5)
    Eligible subjects will receive GSK1827771 via injection
    Intervention: Drug: GSK1827771
  • Placebo Comparator: Subjects receiving placebo in sub-cohort Xc (Cohort 1-5)
    Eligible subjects will receive placebo matching to GSK1827771
    Intervention: Drug: Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
45
April 5, 2008
April 5, 2008   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy adult men or women as determined by a responsible physician, based on a medical evaluation including history, physical examination, laboratory tests and cardiac assessment.
  • Female subjects of non-childbearing potential.
  • Male subjects must agree to abstain from or agree to use adequate contraception, in addition to having their female partner use another form of contraception. This criterion must be followed from the time of the first dose of study medication until Pharmacokinetic levels are determined to be below the LLQ.
  • Men or women who are between 18 and 55 years of age, inclusive.
  • Body Mass Index (BMI) within the range of 18-35 kilogram per meter square (kg/m^2) inclusive.
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form

Exclusion Criteria:

  • The subject has a positive pre-study urine drug/urine alcohol screen. A minimum list of drugs that will be screened for includes amphetamines, barbiturates, cocaine, opiates, cannabinoids and benzodiazepines.
  • A history of regular alcohol consumption averaging >7 drinks/week for females or >14 drinks/week for males. One drink is equivalent to (12 g alcohol) = 5 ounces [150 milliliter (mL)] of wine or 12 ounces (360 mL) of beer or 1.5 ounces (45 mL) of 80 proof distilled spirits
  • The subject is unwilling to abstain from alcohol consumption from 48 hour prior to dosing until discharge from the clinic, and for 48 hour prior to all other out-patient clinic visits.
  • Smoked or used tobacco or nicotine-containing products within the previous 6 months prior to the first dose of current study medication.
  • 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.
  • Previous exposure to or treatment with PEGylated molecules.
  • Use of anti-Tumor Necrosis Factor (anti-TNF) drugs within 60 days prior to dosing.
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) within 7 days , 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 (including antibiotics) which, in the opinion of the investigator and/or GSK Medical Monitor, contraindicates the subject's participation.
  • Positive pregnancy test at Screening or on Day -1 (females only).
  • Any clinically significant abnormality identified on the screening medical assessment or examination, or ECG.
  • Any white blood cell (WBC) or neutrophil count outside the normal range at screening or on Day -1.
  • History of significant cardiac, pulmonary, metabolic, renal, hepatic, or gastrointestinal conditions that in the opinion of the investigator and/or GSK Medical Monitor, places the subject at an unacceptable risk as participant in this trial.
  • History of any autoimmune or current inflammatory conditions including rheumatoid arthritis or any other joint disease.
  • History of malignancy, except for surgically cured basal cell carcinoma or cured cervical carcinoma (> 2 yrs prior to dosing).
  • Currently has asthma or history of chronic obstructive pulmonary disease (COPD).
  • Current evidence of ongoing or acute infection.
  • The subject has a history of repeated, chronic or opportunistic infections which, in the opinion of the investigator and/or GSK Medical Monitor, places the subject at an unacceptable risk as a participant in this trial.
  • History of Mycobacterium tuberculosis or any other previous Mycobacterium infection.
  • A positive pre-study Hepatitis B surface antigen, positive Hepatitis C antibody, or human immunodeficiency virus (HIV) antibody testing result.
  • History of a severe allergic reaction, angio-edema, anaphylaxis or immunodeficiency
  • History of elevated blood pressure or blood pressure >140/90 millimeters of mercury (mmHg) at screening.
  • Corrected QT interval (QTc) > 450 milliseconds.
  • Where participation in study would result in donation of blood in excess of 500 mL within 56 days of starting the study.
  • Subject whose calculated creatinine clearance is less than 80 mL/min
  • Liver function tests above the upper limit of normal at screening (alkaline transaminase (ALT), aspartate transaminase (AST) or bilirubin).
  • Chronic liver or biliary disease, history of Gilbert's syndrome in a previous clinical study or at screening.
Sexes Eligible for Study: All
18 Years to 55 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00539760
110394
No
Not Provided
Not Provided
GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
August 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP