A Two-Part Study to Determine: Best Medication Formulation and Food Effect

Completed · Phase 1

Conditions studied: Overactive Bladder

In brief

This is a two-part study. Part 1 is designed to find the best modified release formulation of GW423753; Part 2 is designed to use the selected formulation(s) from Part 1 to find out if food affects the way the medication is processed by the body.

Key facts

Study ID

NCT00427596

Run by

GlaxoSmithKline

People needed

18

Starts

2007-01-01

Expected to finish

2007-08-01

Last updated by the study team

2008-10-07

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy males \& females
• Part 1 ages 18-60
• Part 2 ages 18-50 \& 65-80
• Within normal weight range given your height
• Negative urine drug and alcohol test
• Willing to follow all study procedures

You may not qualify if…

• Any clinically relevant abnormality identified on the screening physical examination, clinical laboratory tests, 12-lead ECG, or any other medical condition or circumstance making the subject unsuitable for participation in the study based on the Investigator's assessment.
• Subjects with either a blood pressure measurement > 150/90 mmHg, or a history of coronary disease AND a blood pressure > 140/90 mmHg, at screening.
• History of drug or other allergy, which, in the opinion of the Investigator, contraindicates their participation.
• Regular alcohol consumption averaging >/7 drinks/week for women or >/ 14 drinks/week for men (1 drink = 5 ounces of wine or 12 ounces of beer or 1.5 ounces of hard liquor) within 6 months of the first dose of study medication.
• Positive urine drug, alcohol or serum pregnancy test at screening and prior to dosing in each study session.
• Positive for hepatitis C antibody, hepatitis B surface antigen or HIV at screening.
• Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to administration of study medication.
• Use of prescription or non-prescription drugs within 7 days or 5 half-lives (whichever is longer) prior to administration of study medication and during the study. By exception, use of acetaminophen at doses of ≤ 2 grams per day, the use of contraceptives (oral, depots, patches, etc.) and anti-hypertensive medications will be permitted.
• Use of vitamins or herbal/dietary supplements within 7 days prior to administration of study medication and during the study.
• Subject is unable and/or unwilling to adhere to Lifestyle Guidelines
• Subjects who have donated more than 500 mL of blood or plasma within 56 days prior to administration of study medication.
• An unwillingness on the part of male volunteers to abstain from sexual intercourse with pregnant or lactating women; or an unwillingness to use a condom and another form of contraception (e.g., IUD, birth control pills taken by female partner, diaphragm with spermicide) if engaging in sexual intercourse with a woman who could become pregnant from the time of the first dose of study medication until completion of follow-up procedures.
• Pregnant or lactating woman. A pregnancy test will be performed for all women at screening and prior to each dosing session to confirm eligibility.
• The subject has a known hypersensitivity or idiosyncratic reaction to any drug chemical related to this study.

Where it is running

• GSK Investigational Site — Buffalo, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.