Status:
COMPLETED
Safety, Tolerability and Pharmacokinetics of GSK1034702 in Healthy Subjects
Lead Sponsor:
GlaxoSmithKline
Conditions:
Cognitive Disorders
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
This is a First Time in Human Study to assess the safety, tolerability and pharmacokinetics of single doses of GSK1034702 in healthy subjects. It will be a single-blind, randomized, placebo-controlled...
Eligibility Criteria
Inclusion
- Healthy as determined by a responsible physician, based on a medical evaluation including own and familial medical history, physical examination, laboratory tests and cardiac monitoring.
- Male or female between 18 and 55 years of age.
- A female subject is eligible to participate if she is of non-childbearing potential
- Body weight \> 50 kg and BMI within the range 19 - 29.9 kg/m2 (inclusive).
- Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
- Capable of reading, comprehending and writing English at a sufficient level to complete study-related materials.
- Demonstrates no evidence of mental impairment.
- No co-morbid Psychiatric Disorders as defined using the Mini International Neuropsychiatric Interview
Exclusion
- A positive pre-study drug/alcohol screen.
- A positive pre-study Hepatitis B , Hepatitis C or HIV.
- History of regular alcohol consumption.
- 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: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
- 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 .
- History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy.
- Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
- Pregnant females, females planning pregnancy or lactating females.
- Unwillingness or inability to follow the procedures outlined in the protocol.
- History of sensitivity to heparin or heparin-induced thrombocytopenia.
- Subjects with a current or a history of psychiatric illness.
- Subjects with any history of suicidal attempts or behavior.
- Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products.
- Consumption of red wine, seville oranges, grapefruit or grapefruit juice (and pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices) from 7 days prior to the first dose of study medication.
Key Trial Info
Start Date :
May 2 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 15 2008
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00743405
Start Date
May 2 2008
End Date
December 15 2008
Last Update
July 21 2017
Active Locations (1)
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1
GSK Investigational Site
London, United Kingdom, NW10 7NS