A Study Of GSK679586A When Infused Into Healthy And Mild Asthmatic Volunteers

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. Identifier: NCT00411814
Recruitment Status : Completed
First Posted : December 15, 2006
Last Update Posted : March 19, 2012
Information provided by (Responsible Party):

Brief Summary:
This is a two part study. Part I is designed to test single doses of GSK678586A in healthy volunteers. Part II is designed to test repeat doses (two doses) of GSK679586A in patients with mild asthma. Both parts are designed to investigate the safety, tolerability and the way the body absorbs GSK679586A when given by intravenous infusion (through a vein in your arm).

Condition or disease Intervention/treatment Phase
Asthma Drug: GSK679586 Drug: Placebo Phase 1

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 56 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Dose-escalating Study of the Safety and Pharmacokinetics of GSK679586A in Healthy Volunteers and Mild Asthmatics.
Study Start Date : November 2006
Actual Primary Completion Date : February 2008
Actual Study Completion Date : February 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Asthma
U.S. FDA Resources

Arm Intervention/treatment
Placebo Comparator: Placebo
Drug: Placebo
Other Name: Saline
Active Comparator: Active
Drug: GSK679586
Active Drug

Primary Outcome Measures :
  1. Safety and tolerability in healthy volunteers.Assessed using clinical safety assessments and blood and urine analysis [ Time Frame: Throughout the study ]
  2. Safety and tolerability in mild asthmatics.Assessed using clinical safety assessments and blood and urine analysis. [ Time Frame: Throughout the study ]

Secondary Outcome Measures :
  1. Blood sampling [ Time Frame: Throughout the study ]
  2. Effects on blood and lung function. [ Time Frame: Throughout the study ]
  3. Lung function [ Time Frame: Throughout the study ]
  4. Plasma levels of GSK679586A to determine pharmacokinetic parameters [ Time Frame: Throughout the study ]
  5. serum antibodies to GSK679586A [ Time Frame: Throughout the study ]

Information from the National Library of Medicine

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

Inclusion criteria:

  • Men aged 18 - 65 years inclusive, or women aged 18 - 50 years inclusive.
  • Female subjects must be of non-childbearing potential,
  • Male subjects must agree to abstain from sexual intercourse or use adequate contraception during sexual intercourse with pregnant or lactating females, in addition to their female partner using another form of contraception. This criterion must be followed from the time of the first dose of study medication until 84 days after the last dose of study medication.
  • Body weight ≥ 50 kg and BMI within the range 19 - 29.9 kg/m2.
  • Non-smoker as verified by urinary cotinine levels below 300 ng/mL at screening or ex-smokers who have given up smoking for >12 months with a history <10 pack years [Pack yrs = (No of cigarettes/day x No of years smoked)/20]
  • Available to complete all study measurements.
  • Able to read, comprehend, and write English at a sufficient level to complete study related materials.
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form

Additional Inclusion Criteria for Subjects in Part I

• Healthy as determined by a responsible physician, based on a medical evaluation including history, physical examination, laboratory tests, cardiac monitoring.

Additional Inclusion Criteria for Subjects in Part II

  • History of asthma for at least 6 months prior to the screening visit currently requiring no treatment or intermittent treatment with inhaled short-acting beta2-agonist only. Subject must not have received low dose inhaled corticosteroids within three months prior to Day 0.
  • Pre-bronchodilator FEV1 >70% but <90% of predicted at screening with ≥12% reversibility after short-acting beta2-agonist or If the subject has a pre-bronchodilator FEV1 ≥90% at screening but has a history of asthma or if the subject meets the FEV1 criteria but does not demonstrate ≥12% reversibility after short-acting beta2-agonist administration, then the subject may be considered eligible if a Bronchial Provocation Test for asthma is positive (and after consultation with Medical Monitor and Principal Investigator). The bronchial provocation will be considered positive when the standard criteria for a positive response with the given challenge agent are met.
  • Skin prick test positive for an allergen that is appropriate for nasal challenge

Exclusion criteria:

  • As a result of medical interview, physical examination or screening investigations, the responsible physician deemed the subject unsuitable for the study.
  • 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 physician responsible, contraindicates their participation.
  • Previous exposure to humanised antibody therapy for any reason.
  • A strong family history of Th1 cytokine-related inflammatory disorders, including but not limited to, Type I diabetes mellitus, multiple sclerosis, Crohn's disease, rheumatoid arthritis, sarcoidosis.
  • Known history of active or latent tuberculosis, or recent (within 6 months of study enrolment) exposure to a person with active tuberculosis. Previous medical history and letter from the subject's physician (GP) should exclude this.
  • A history of chronic urogenital infections or other chronic infections.
  • Subjects who have received any type of vaccination in the last two months.
  • 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
  • Where participation in study would result in donation of blood in excess of 500 mL within a 56 day period
  • 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'sWort) 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 sponsor the medication will not interfere with the study procedures or compromise subject safety.
  • History of alcohol/drug abuse or dependence within 12 months of the study:
  • Abuse of alcohol defined as an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units (males) or defined as an average weekly intake of greater than 14 units or an average daily intake of greater than 2 units (females). 1 unit is equivalent to a half-pint (220mL) of beer or 1 (25ml) measure of spirits or 1 glass (125ml) of wine
  • A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
  • A positive test for human immunodeficiency virus (HIV) antibodies.
  • The subject has a positive pre-study urine drug/ urine alcohol screen. A minimum list of drugs that will be screened for include Amphetamines, Barbiturates, Cocaine, Opiates, Cannabinoids and Benzodiazepines.
  • ECG that is outside of ranges as defined by the protocol
  • Those who, in the opinion of the Investigator, have a risk of non-compliance with study procedures.
  • The subject has a history of confirmed or active parasitic infection.
  • The subject is unable to refrain from travelling to countries with a high prevalence of infectious (especially parasitic) disease from when the first dose is administered until the expected washout period is complete (plasma levels below LLQ) or the last follow-up visit, which ever is later

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 identifier (NCT number): NCT00411814

Australia, New South Wales
GSK Investigational Site
Randwick, New South Wales, Australia, 2031
Australia, Victoria
GSK Investigational Site
Melbourne, Victoria, Australia, 3004
Sponsors and Collaborators
Study Director: GSK Clinical Trials GlaxoSmithKline

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: GlaxoSmithKline Identifier: NCT00411814     History of Changes
Other Study ID Numbers: I13105054
First Posted: December 15, 2006    Key Record Dates
Last Update Posted: March 19, 2012
Last Verified: January 2012

Keywords provided by GlaxoSmithKline:
Safety and pharmacokinetic study,
mild asthmatic patients,

Additional relevant MeSH terms:
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
Hypersensitivity, Immediate
Immune System Diseases