This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback

Relative Bioavailability and Food Effect Study for GSK163090 in Healthy Male and Female Volunteers

This study has been completed.
Information provided by:
GlaxoSmithKline Identifier:
First received: September 27, 2007
Last updated: October 13, 2010
Last verified: October 2010
The study will consist of a screening period, 3 treatment periods and a post-treatment follow-up. In each of the 3 treatment periods, subjects will receive a single oral dose of GSK163090 in the fed or fasted state, followed by a 7-day wash-out period between each dose

Condition Intervention Phase
Depression Anxiety Disorder Drug: GSK163090 Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: An Open Label, Randomised, Single Dose, Three-way Crossover Study to Investigate the Relative Bioavailability of Two Different Formulations of GSK163090 and the Effect of Food on the Pharmacokinetics of a Tablet Formulation in Healthy Male and Female Volunteers

Resource links provided by NLM:

Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Pharmacokinetic parameters for GSK163090. Pharmacokinetic blood samples will be collected up to 72 hours post-dose following each dosing session. [ Time Frame: 72 hours post-dose following each dosing session. ]

Secondary Outcome Measures:
  • Additional pharmacokinetic parameters, safety, and tolerability. [ Time Frame: 72 hours post-dose following each dosing session. ]

Enrollment: 16
Study Start Date: September 2007
Study Completion Date: November 2007
Primary Completion Date: November 2007 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Healthy male or female subjects between the ages of 18 and 55 years inclusive.
  • If female, the subject is eligible to enter and participate in this study if she is not lactating and is of Non-childbearing potential or
  • Child-bearing potential, has a negative pregnancy test at both screen and baseline and agrees to adequate contraception:
  • Body weight ≥ 50 kg and body mass index (BMI) between 18.5 - 29.9 kg/m2 inclusive.
  • Capable of giving informed consent and can comply with the study requirements and timetable.
  • Self-administered Beck Depression Inventory II scale total score no greater than 9, and suicide question score of zero.
  • The subject must be able to read, comprehend and record information.
  • A signed and dated written informed consent is obtained from the subject.
  • Non-smoker (abstinence from smoking for at least 6 months before the start of the study).
  • Agrees to abstain from ingesting caffeine or xanthine-containing products for 24 hours prior to the start of dosing until collection of the final pharmacokinetic sample.
  • Agree to abstain from alcohol for 24 hours prior to the start of dosing until collection of the final pharmacokinetic sample

Exclusion Criteria:

  • As a result of any of the medical interview, physical examination or screening investigations the physician responsible considers the subject unfit for the study.
  • The subject has a history of a drug or other allergy which in the opinion of the physician responsible contraindicates their participation in the study.
  • The subject is currently participating or has participated in a clinical trial with a new chemical entity during the previous 4 months or any other trial during the previous 3 months.
  • The subject has a screening ECG with values outside of protocoled ranges
  • The subject has a pulse rate <45 or >100 bpm and a systolic blood pressure >150 and <90 and a diastolic blood pressure >90 and <50.
  • History of long QT syndrome (personal or family) or other cardiac conduction disorder, or other clinically significant cardiac disease.
  • The subject has liver function tests (LFT) elevated >1.5 times above the reference range at pre-study screening that remain elevated with a repeat LFT.
  • Any other clinically significant laboratory abnormality.
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) 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.
  • Abuse of alcohol defined as an average weekly intake of greater than 21 units for males and 14 units for females or an average daily intake of greater than 3 units for males and 2 units for females. 1 unit is equivalent to a half-pint (220mL) of beer or 1 (25ml) measure of spirits or 1 glass (125ml) of wine.
  • Consumption of grapefruit juice or grapefruit within 7 days prior to the first dose of study medication until collection of the last PK sample.
  • The subject is unable to abstain from strenuous physical activity for 48 h prior to screening and follow up and for 48 h prior to and 48 h after each treatment period.
  • Where participation in study would result in donation of blood in excess of 500 mL within a 90 day period
  • An unwillingness of male subjects to abstain from, or use adequate contraception during, sexual intercourse with pregnant or lactating women from the time of the first dose of study medication until 90 days following administration of the last dose of study medication OR An unwillingness of the male subject to use a adequate contraception 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 study medication until 90 days following administration of the last dose of study medication.
  • Current or recent (within one year) gastrointestinal disease; a history of malabsorption, esophageal reflux, irritable bowel syndrome; frequent (more than once a week) occurrence of heartburn; or any surgical intervention (e.g., cholecystectomy) which would be expected to influence the absorption of drugs.
  • The subject has a history of psychiatric illness
  • Any history of suicidal attempts or behavior.
  • The subject has tested positive for hepatitis C antibody or hepatitis B surface antigen.
  • The subject has tested positive for HIV.
  • The subject has a past history of drug abuse or has tested positive for urine drugs of abuse at pre-study screening.
  • The subject has any history of serotonin syndrome.
  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 identifier: NCT00536679

GSK Investigational Site
Neuss, Nordrhein-Westfalen, Germany, 41460
Sponsors and Collaborators
Study Director: GSK Clinical Trials, MD GlaxoSmithKline
  More Information

Responsible Party: Study Director, GSK Identifier: NCT00536679     History of Changes
Other Study ID Numbers: 103268
Study First Received: September 27, 2007
Last Updated: October 13, 2010

Keywords provided by GlaxoSmithKline:
Relative Bioavailability
Food Effect

Additional relevant MeSH terms:
Anxiety Disorders
Mental Disorders processed this record on June 23, 2017