Study to Determine the Effect of Repeated Administration of Diltiazem on the Pharmacokinetics of Darapladib (Sb-480848).

Exclusion Criteria

• •A subject will not be eligible for inclusion in this study if any of the following criteria apply:
• •Criteria Based Upon Medical Histories
• •Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
• •History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of \>14 drinks for males or \>7 drinks for females. One drink is equivalent to 12 g of alcohol: 12 ounces (360 ml) of beer, 5 ounces (150 ml) of wine or 1.5 ounces (45 ml) of 80 proof distilled spirits.
• •History of sensitivity to heparin or heparin-induced thrombocytopenia.
• •History of sensitivity to any of the study medications, including diltiazem, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
• •Any contraindications for diltiazem administration.
• •Any condition that, in the opinion of the investigator, presents undue risk from the study medications, including diltiazem, or procedures.
• •Requiring the use of oral or injectable strong Cytochrome P450 (CYP3) A4 inhibitors or use of other CYP3A4 inhibitor/inducers within 14 days prior to dosing.
• •History of anaphylaxis, anaphylactoid (resembling anaphylaxis) reactions
• •Clinical criteria for diagnosing anaphylaxis or severe allergic response. Criteria Based Upon Diagnostic Assessments
• •A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
• •A positive pre-study drug/alcohol screen.
• •A positive test for human immunodeficiency virus (HIV) antibody.
• •Pregnant females as determined by positive human chorionic gonadotropin (hCG) test at screening or prior to dosing.
• •Other Criteria
• •Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
• •Lactating females.
• •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.
• •Unable to refrain from the 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 GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
• •Unwillingness or inability to follow the procedures outlines in the protocol.
• •Subject is mentally or legally incapacitated.
• •Consumption of grapefruit or grapefruit juice within 7 days prior to the first dose of study medication.