
A5227 (Females only)
The Effect of Prior Short Course Combination Antiretroviral Therapy Administered for the Prevention of Mother-to-Child Transmission (pMTCT) of HIV-1 on Subsequent Treatment Efficacy in Treatment -"Nearly Naļve" Participants
Who Can Enroll: Women who were previously treated with short-term HIV therapy to prevent MTCT during pregnancy. Now require long term HIV tx. VL>500 No HAART within 6 months of study entry.
Study Therapy: Efavirenz plus Truvada. All meds provided by study.
Study RN: Please contact Karen Savage at 205-975-7925.
A5257
A Phase III Comparative Study of Three Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI)-Sparing Antiretroviral Regimens for Treatment-Naļve HIV-1-Infected Volunteers.
Who Can Enroll: ARV treatment naļve requiring therapy. VL >1000 Any CD4.
Study Therapy: Truvada plus either Raltegravir, ATZ/r or DRZ/r (all meds but ritonovir provided by study with co-pay reimbursed).
Study RN: Please contact Karen Savage at 205-975-7925.
A5262
A Pilot Efficacy and Safety Trial of Raltegravir Plus Darunavir/r for Treatment-Naļve HIV-1 Infected Subjects.
Who Can Enroll: HIV Treatment Naļve Renal Dysfunction OK (Not HD or PD). VL >/= 5000 Any CD4.
Study Therapy: Raltegravir plus Darunavir/r.
Study RN: Please contact Karen Savage at 205-975-792.
Merck Acute Infection
A Randomized Pilot Study of Raltegravir/Tenofovir/Emtricitibine versus Efavirenz/Tenofovir/Emtricibine for Adults with Acute HIV-1 Infection: Exploring the Role of Integrase Inhibition in Early HIV Pathogenesis.
Who Can Enroll: Acute or Early HIV Infection. VL>5000 Any CD4.
Study Therapy: Raltegravir vs Sustiva in combination with Truvada (Raltegravir supplied by study).
Study RN: Please contact Kerry Upton at 205-975-9128.
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