A Comparison of 141W94 and Indinavir in HIV-Infected Patients
HIV Infections

About this trial
This is an interventional treatment trial for HIV Infections focused on measuring HIV-1, Drug Therapy, Combination, HIV Protease Inhibitors, Indinavir, RNA, Viral, VX 478, Reverse Transcriptase Inhibitors, Anti-HIV Agents, Viral Load
Eligibility Criteria
Inclusion Criteria Patients must have: Documented HIV infection. HIV RNA >= 400 copies/ml within 14 days prior to randomized study drug administration. No active AIDS-defining opportunistic infection or disease. Signed, informed consent from parent or legal guardian of patients less than 18 years of age. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Unlikely to complete the randomized dosing period. Malabsorption syndrome or other gastrointestinal dysfunction that might interfere with drug absorption or ability to take oral medications. Serious medical conditions (e.g., diabetes, cardiac dysfunction, hepatitis) that would compromise patient safety. Concurrent Medication: Excluded: Cytotoxic chemotherapeutic agents (except local treatment for Kaposi's sarcoma). Investigational treatments (treatment through Treatment IND or expanded-access programs are evaluated individually). Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons. Terfenadine, astemizole, cisapride, triazolam, midazolam, and ergotamine/dihydroergotamine-containing regimens. Concurrent Treatment: Excluded: Radiation therapy (except local treatment for Kaposi's sarcoma). Patients with the following prior conditions are excluded: Clinically relevant pancreatitis or hepatitis within the last 6 months. Prior Medication: Excluded: Cytotoxic chemotherapeutic agents within 30 days of study drug administration (except local treatment for Kaposi's sarcoma). Protease inhibitor therapy. Dose of vaccine through an investigational HIV vaccine trial within the 3 months prior to study drug administration. Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons within 30 days of study drug administration. Prior Treatment: Excluded: Radiation therapy within 30 days prior to study drug administration (except local treatment for Kaposi's sarcoma). Risk Behavior: Excluded: Current alcohol or illicit drug use that may interfere with drug absorption or ability to take oral medication. Required: NRTI therapy at day of entry and up to screening. Required: >= 12 weeks of NRTI therapy.
Sites / Locations
- East Bay AIDS Ctr
- AIDS Healthcare Foundation
- Saint Francis Mem Hosp
- ViRx Inc
- Univ of Colorado Health Sciences Ctr
- Whitman Walker Clinic Inc
- CRI of South Florida
- Community Research Initiative of Central Florida
- Univ of Miami Dept of Medicine
- Northwestern Univ Med School
- Tulane Univ Med School
- Boston Med Ctr / Evans - 556
- Beth Israel Deaconess Med Ctr
- Univ of Nebraska Med Ctr
- Community Research Initiative on AIDS
- Harlem Hosp
- The Nalle Clinic / Clinical Research Dept
- Med College of Ohio / Division of Infectious Diseases
- The Research and Education Group
- Methodist Hosp
- Community Oriented Primary Care
- Univ of Texas Med Branch
- Baylor College of Medicine / Dept of Medicine
- Hampton Roads Med Specialists