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| Sponsor: | Abbott |
|---|---|
| Information provided by: | Abbott |
| ClinicalTrials.gov Identifier: | NCT00002223 |
Purpose
The purpose of this study is to determine how many HIV-infected patients continue taking ritonavir/indinavir combination after having taken indinavir three times a day as part of their anti-HIV drug therapy. This study also examines the safety and effectiveness of the ritonavir/indinavir combination.
| Condition | Intervention |
|---|---|
|
HIV Infections |
Drug: Indinavir sulfate Drug: Ritonavir |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety Study Primary Purpose: Treatment |
| Official Title: | Ritonavir (ABT-538)/Indinavir Combination Treatment in HIV-Infected Patients Previously Receiving Indinavir 800 mg TID |
Eligibility| Ages Eligible for Study: | 12 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with any of the following symptoms or conditions are excluded:
Any condition that in the opinion of the investigator may obscure proper observation of the safety or activity of the treatment regimens used in this study.
Concurrent Medication:
Excluded:
Patients with the following prior conditions are excluded:
Prior Medication:
Excluded:
Prior treatment with ritonavir.
Risk Behavior:
Excluded:
History of active substance abuse (i.e., recreational drugs or alcohol).
Included:
- Indinavir 800 mg three times a day plus unspecified nucleosides for at least 3 months.
Contacts and Locations| United States, California | |
| AIDS Healthcare Foundation | |
| Los Angeles, California, United States, 90027 | |
| Tower Infectious Diseases | |
| Los Angeles, California, United States, 90048 | |
| United States, Florida | |
| Urgent Care Ctr / North Broward Hosp District | |
| Fort Lauderdale, Florida, United States, 33316 | |
| Goodgame Med Ctr / Central Florida Research Initiati | |
| Maitland, Florida, United States, 32751 | |
| United States, New York | |
| Mount Sinai Med Ctr | |
| New York, New York, United States, 10029 | |
| United States, Pennsylvania | |
| Stephen Hauptman | |
| Philadelphia, Pennsylvania, United States, 19107 | |
More Information
| ClinicalTrials.gov Identifier: | NCT00002223 History of Changes |
| Other Study ID Numbers: | 245E, M98-823 |
| Study First Received: | November 2, 1999 |
| Last Updated: | February 19, 2009 |
| Health Authority: | United States: Food and Drug Administration |
|
Drug Therapy, Combination Adolescent Behavior HIV Protease Inhibitors Ritonavir Indinavir |
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases HIV Protease Inhibitors |
Indinavir Ritonavir Protease Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Anti-HIV Agents Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Therapeutic Uses |