A Pilot Study to Characterize the Pharmacokinetics of Raltegravir in the Cervicovaginal Fluids of HIV-infected Women

Inclusion Criteria: * HIV-1 infection documented by HIV serology or detectable viral load * Self-described as African-American * Less than 7 days cumulative of prior HIV therapy * Plasma HIV RNA PCR equal to or greater than 1000 copies/mL within 90 days prior to study entry * Able to provide informed consent * In the opinion of the investigator, able to comply with study medication and procedures * ALT (SGPT) \< or equal to 3.0 x ULN within 45 days prior to study entry * GRF \> 60 as calculated by MDRD within 45 days prior to study entry * All women of reproductive potential (who have not reached menopause or undergone hysterectomy, bilateral oophorectomy, or tubal ligation) must have a negative serum or urine β-HCG pregnancy test performed within 48 hours before entry. All study volunteers must agree not to participate in a conception process (e.g., active attempt to become pregnant or to impregnate, sperm donation, in vitro fertilization) and, if participating in sexual activity that could lead to pregnancy, the female study volunteer/male partner must use at least one reliable method of contraception (e.g., condoms, with or without a spermicidal agent; a diaphragm or cervical cap with spermicide; an IUD; or hormonal-based contraception), simultaneously while receiving the protocol-specified medication(s) and for 6 weeks after stopping the medication(s). Exclusion Criteria: * Pregnancy * Breastfeeding * Prior receipt of Raltegravir * Any condition which in the opinion of the investigator is likely to interfere with follow-up or ability to take the study medication appropriately * A positive test for bacterial vaginosis, syphilis, gonorrhea, Chlamydia, HSV-2 (active lesions), or trichomonas at entry or week 2 of the main study, CID 0706