Study of SB-742457 or Donepezil Versus Placebo in Subjects With Mild-to-moderate Alzheimer's Disease


Tracking Information

Start Date  ICMJEJuly 2008
Estimated Primary Completion DateMay 2010   (final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: April 30, 2009)
Assessment of cognition and global function after 24 weeks treatment [ Time Frame: 24 weeks ]
Original Primary Outcome Measures ICMJE 
 (submitted: June 30, 2008)
Assessment of cognition and global function after 24 weeks treatment
Change HistoryComplete list of historical versions of study NCT00708552 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ICMJE 
 (submitted: April 30, 2009)
Assessment of cognition and global function after 12 and 24 weeks treatment. Activities of daily living, assessment of depressive symptoms. Safety and tolerability. Pharmacokinetics and exploratory pharmacogenetics. [ Time Frame: 24 weeks ]
Original Secondary Outcome Measures ICMJE 
 (submitted: June 30, 2008)
Assessment of cognition and global function after 12 and 24 weeks treatment. Activities of daily living, assessment of depressive symptoms. Safety and tolerability. Pharmacokinetics and exploratory pharmacogenetics.

Descriptive Information

Brief Title  ICMJEStudy of SB-742457 or Donepezil Versus Placebo in Subjects With Mild-to-moderate Alzheimer's Disease
Official Title  ICMJEStudy AZ3110865, a Study Comparing SB-742457 or Donepezil Versus Placebo in Subjects With Mild-to-moderate Alzheimer's Disease
Brief Summary

The study is designed to investigate the efficacy, safety and tolerability of SB-742457 versus placebo in subjects with mild-to-moderate Alzheimer's disease. SB-742457 is an experimental treatment which increases the levels of certain chemicals in the brain that are often decreased in patients with Alzheimer's disease.

Detailed Description 
Study PhasePhase II
Study Type  ICMJEInterventional
Study Design  ICMJETreatment, Randomized, Double Blind (Subject, Investigator), Parallel Assignment, Safety/Efficacy Study
Condition  ICMJEAlzheimer's Disease
Intervention  ICMJE
  • Drug: Donepezil
    investigational drug
  • Drug: Placebo
    comparator
    Other Names:
    • Placebo
    • SB-742457
    • Donepezil
  • Drug: SB-742457
    investigational drug
Study Arms / Comparison Groups
  • arm 2: Placebo Comparator
    Intervention: Drug: Placebo
  • arm 1: Experimental
    Interventions:
    • Drug: Donepezil
    • Drug: SB-742457

Recruitment Information

Estimated Enrollment  ICMJE576
Estimated Completion DateMay 2010
Estimated Primary Completion DateMay 2010   (final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion criteria:

  • Subjects and their caregivers must provide informed consent prior to study entry.
  • Subjects must have a clinical diagnosis of probable mild-to-moderate Alzheimer's disease with a documented 6-month history of AD symptoms
  • Subjects must have a regular caregiver who is willing to attend visits, oversee the subject's compliance with the study and report on the subject's status.
  • Female subjects of child-bearing potential must agree to pregnancy testing and approved form of birth control.

Exclusion criteria:

  • Diagnosis of possible, probable or definite vascular dementia.
  • History/evidence of any other CNS disorder that could be interpreted as a cause of dementia
  • History of known or suspected seizures, loss of consciousness or significant head trauma
  • Subjects with ECG, blood pressure and laboratory values outside of protocol criteria are excluded.
  • Subjects with known photosensitivity
  • Subjects with a history of previous exposure to SB-742457, taking agents for which there is a theoretical risk of interaction with SB-742457, or taking medication for Alzheimer's disease or centrally acting agents which might impact study outcomes may not participate.
GenderBoth
Ages50 Years to 85 Years
Accepts Healthy VolunteersNo
Contacts  ICMJE
Contact: US GSK Clinical Trials Call Center877-379-3718
Location Countries  ICMJEBulgaria,   Chile,   Czech Republic,   Estonia,   Germany,   Greece,   Korea, Republic of,   Mexico,   Poland,   Russian Federation,   South Africa

Administrative Information

NCT ID  ICMJENCT00708552
Responsible PartyStudy Director, GSK
Study ID Numbers  ICMJEAZ3110865
Study Sponsor  ICMJEGlaxoSmithKline
Collaborators  ICMJE 
Investigators  ICMJE
Study Director:GSK Clinical TrialsGlaxoSmithKline
Information Provided ByGlaxoSmithKline