A Phase II, Double-Blind RAndomized, Placebo-Controlled Study to Evaluate the Antiviral Activity, Safety, Tolerability, and Pharmacokinetics of GW873130 for 10 Days in HIV-1 Infected Adults

Date de début de l'étude : 1 janvier 2004

INCLUSION CRITERIA: A subject will be eligible for inclusion in this study only if all of the following criteria apply: 1. Healthy adult male aged greater than or equal to 18 OR Healthy adult female aged greater than or equal to 18, of non-childbearing potential, defined as: Women who are surgically sterile or are post-menopausal, as indicated by history of no menses for a minimum of one year from the date of the screening visit. Healthy adult female aged greater than or equal to 18 of childbearing potential, who agrees to use double barrier method (e.g. condom+diaphragm) starting from the screening visit through the follow up visit (Day 24). Note: Spermicides and/or hormonal contraceptives will not be considered sufficient forms of contraception for this study. 2. Screening plasma HIV-1 RNA greater than or equal to 5,000- less than or equal to 250,000 copies/mL. 3. Viral load within the past 30-90 days of the screening visit must be within 0.5log of screening HIV-1 RNA. 4. Not taken any antiretroviral therapy for the preceding 3 months from screening visit. 5. CD4 cell count greater than or equal to 200 cells/mm(3) with a historical nadir greater than or equal to 200 cells/mm(3). 6. CCR5-tropic virus based on viral tropism assessment at screening visit. 7. Normal resting 12-lead electrocardiogram at screening visit. 8. Signed and dated written informed consent prior to admission to the study. 9. In addition to the inclusion criteria listed above, patients must meet the following inclusion criteria: * Willingness and ability to fast for 10 hours except for water from 9:00 p.m. until 7:00 a.m. during eight of the study days. * Willingness and ability to eat a 30% fat diet during the 10 day treatment period of the study. * Willingness to allow stored blood samples to be used in the future for further testing or for studying HIV disease and immune function. EXCLUSION CRITERIA: A subject will not be eligible for inclusion in this study if any of the following criteria apply: 1. CXCR4 tropic virus based on viral tropsin assessment at screening visit. 2. Chronic diarrhea (greater than 3 stools/day) 3. Subject with history of oropharyngeal candidiasis or C AIDS-defining illness according to the 1993 Centers for Disease Control (CDC) AIDS surveillance definition. 4. Greater than two prior ARV regimens. 5. Any acute laboratory abnormality at screen which, in the opinion of the investigator, should preclude the subject's participation in the study of an investigational compound. Any grade 4 laboratory abnormality at screen will exclude a subject from study participation unless the investigator can provide a compelling explanation for the laboratory result(s) and has the assent of the sponsor. 6. Significant blood loss (1 pint of whole blood) within 56 days of the screening visit of the study. 7. Previous participation in an experimental drug trial(s) within 30 days of the screening visit of the study. 8. Any conduction delay, regardless of clinical significance on screening ECG. 9. History of clinically relevant pancreatitis or hepatitis within the previous 6 months. 10. Any condition which, in the opinion of the investigator, may interfere with the subject's ability to comply with the dosing schedule and protocol evaluations (including alcohol or drug abuse) or which might compromise the safety of the subject. 11. Any condition which, in the opinion of the investigator, might interfere with the absorption, distribution, metabolism or excretion of the drug such as diabetes mellitus, hyperthyroidism, malabsorption syndrome, etc. 12. History of cholecystectomy, cholelithiasis or cholecystitis. 13. Any immunization within 30 days prior to first dose of investigational product. 14. History of a drug or other allergy which in the opinion of the investigator, contraindicates the subject's participation in the study or known hypersensitivity to any study medication. 15. Treatment with radiation therapy or cytotoxic chemotherapeutic agents within 30 days of investigational product administration or anticipated need for such treatment within the study. 16. Treatment with immunomodulating agents (such as interleukins, interferons) or any agents with known anti-HIV activity (such as hydroxyurea, foscarnet, or NRTIs) within 30 days of investigational product administration. 17. Use of steroids (oral) within 30 days of first dose of investigational product. 18. Prior treatment with any entry, attachment or fusion inhibitor, experimental or approved. 19. Pregnant women or women who are breastfeeding. 20. Subjects who cannot refrain from drinking grapefruit juice or eating grapefruit within 3 days prior to the first dose of study medication until collection of the final pharmacokinetic blood sample. 21. Use of prescription or non-prescription medications that are not on the GSK APPROVED MEDICATION LIST for GW873140. Medications that are not approved on this list, will need to be discontinued 7 days prior to first dose of investigational product (for drugs that are non-hepatic inducers) and 30 days prior to first dose of investigational product (for drugs that are hepatic inducers) through 5 days post dose. To clarify the exclusion of patients with hepatitis and pancreatitis, the following patients will be excluded: * Patients with a diagnosis of acute viral hepatitis infection in the preceding six months * Patients with a history of AST or ALT elevation five times normal or greater in the the preceding six months * Patients who have been diagnosed with pancreatitis in the preceding six months or have had an elevation of lipase two times normal or greater and symptoms suggestive of pancreatitis (i.e. nausea, vomiting, epigastric pain). Patients with evidence of chronic hepatitis B or C are not excluded from study participation if they are clinically asymptomatic, liver enzymes are less than five times normal, and they have no evidence of hepatic synthetic dysfunction (i.e. PT less than 1.5 times upper limit of normal).