A Study To Look At The Safety Of SB-681323 In Healthy Adult Subjects After Intravenous Administration Of A Single Dose

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00439881
First received: February 23, 2007
Last updated: May 31, 2012
Last verified: February 2011
  Purpose

SB-681323 inhibits the action of an enzyme which is known to contribute to the inflammation seen in such conditions as Chronic Obstructive Pulmonary Disease and Rheumatoid Arthritis. This study will explore the safety of this drug and its blood levels when given in intravenous form to healthy human volunteers.


Condition Intervention Phase
Arthritis, Rheumatoid
Inflammation
Drug: SB-681323
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Official Title: A Study to Assess the Safety and Tolerability of SB-681323 Administered Via the Intravenous Route

Resource links provided by NLM:


Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Safety of SB-681323 in terms of frequency/ nature of adverse events and changes in ECG patterns, vital signs and clinical laboratory parameters (including liver function tests) seen upto 48h after a single intravenous dose.

Secondary Outcome Measures:
  • Regular measurements of SB-681323 blood levels upto 48h after a single intravenous dose. Effects of SB-681323 in blood samples drawn upto 24h after intravenous dosing, on laboratory tests designed to explore the anti-inflammatory properties of the drug.

Estimated Enrollment: 16
Study Start Date: October 2006
Intervention Details:
    Drug: SB-681323
    Other Name: SB-681323
  Eligibility

Ages Eligible for Study:   25 Years to 55 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • A healthy male aged between 25 and 55 years, inclusive, at the time of screening.
  • Body weight = 60 kg and a Body Mass Index within the range of 19 to 32 kg/m2 inclusive.
  • Must have given informed consent and signed the study consent form prior to taking part in any study procedures.
  • Have no significant abnormality on clinical examination.
  • Show no abnormality on haematology, clinical chemistry or urinalysis examination at the pre-study medical examination.
  • Demonstrate a clinically normal 12-lead ECG at screening
  • Liver function tests within the reference range at screening (ALT, AST, ALP, GT and bilirubin)
  • Do not show evidence of pre-study HIV and hepatitis B and C at screening
  • Do not show a positive pre-study urine drug screen

Exclusion Criteria:

  • Taken prescription or over-the-counter medication within 5 days (or 5 half lives, whichever is longer) before the first dosing day, unless the investigator confirms that it will not introduce additional risk or interfere with the study procedures or outcome.
  • Show a history or evidence of drug or alcohol abuse.
  • Show a history of increased liver function tests (ALT, AST, bilirubin) above upper limit of normal (ULN) in the past 6 months (if known).
  • Demonstrate a history of regular alcohol consumption exceeding an average weekly intake of > 21 units (or an average daily intake of greater than 3 units). 1 unit is equivalent to a half-pint (284mL) of beer/lager; 25mL measure of spirits or 125mL of wine.
  • Have a history or presence of any medically significant disease, or any disorder that would introduce additional risk or interfere with the study procedures or outcome. In particular, gastro-intestinal, hepatic or renal disease or other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
  • Exposure prior to the first dosing day to more than 3 new medicinal entities within 12 months or has participated in a study with a new medicinal entity within 3 months or any other study within 2 months.
  • If participation in the study will result in the subject having donated more than 450 mL blood within a 3 month period.
  • On physical examination the subject is observed to have poor venous access.
  • An unwillingness of subjects to abstain from sexual intercourse with women; or unwillingness of the subject to use a condom/spermicide in addition to having their female partner use another form of contraception if the woman could become pregnant from the time of the first dose of investigational product until completion of the follow-up procedures.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00439881

Locations
United Kingdom
GSK Investigational Site
London, United Kingdom, NW10 7NS
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

No publications provided

Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT00439881     History of Changes
Other Study ID Numbers: RA1107570
Study First Received: February 23, 2007
Last Updated: May 31, 2012
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency

Keywords provided by GlaxoSmithKline:
inflammation,
intravenous,
Chronic Obstructive Pulmonary Disease,
P38 inhibitor
SB-681323,
rheumatoid arthritis,

Additional relevant MeSH terms:
Arthritis
Arthritis, Rheumatoid
Inflammation
Autoimmune Diseases
Connective Tissue Diseases
Immune System Diseases
Joint Diseases
Musculoskeletal Diseases
Pathologic Processes
Rheumatic Diseases

ClinicalTrials.gov processed this record on October 30, 2014