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A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Indinavir sulfate
Ritonavir
Sponsored by
Abbott
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Drug Therapy, Combination, Adolescent Behavior, HIV Protease Inhibitors, Ritonavir, Indinavir

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients must have: HIV infection. CD4 cell count greater than 100 cells/microliter. HIV RNA levels greater than 400 copies/microliter using the Roche Ultrasensitive assay. No acute illness. Consent of parent or guardian if less than legal age. No prior enrollment in this study. All entry criteria for this study met within 15 days prior to enrollment. 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: Concurrent non-nucleoside reverse transcriptase inhibitors as part of the antiretroviral regimen. Any of the following medications with ritonavir: midazolam, clorazepate, diazepam, estazolam, flurazepam, triazolam, zolpidem, quinidine, amiodarone, encainide, flecainide, propafenone, bepridil, terfenadine, astemizole, cisapride, bupropion, clozapine, rifabutin, meperidine, propoxyphene, piroxicam, pimozide, dihydroergotamine, and ergotamine. Any of the following medications with indinavir: terfenadine, astemizole, cisapride, triazolam, midazolam. No requirement for rifampin or ketoconazole. Any concurrent treatment with other protease inhibitors. Other concurrent medication (including over-the-counter medicine or alcohol) without the knowledge and permission of the primary investigator. Patients with the following prior conditions are excluded: History of significant drug hypersensitivity. Psychiatric illness that precludes compliance with the protocol. Receipt of investigational drug within 30 days prior to administration of study drug. History of acute or chronic pancreatitis. Anticipation of poor patient compliance with protocol. 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.

Sites / Locations

  • AIDS Healthcare Foundation
  • Tower Infectious Diseases
  • Urgent Care Ctr / North Broward Hosp District
  • Goodgame Med Ctr / Central Florida Research Initiati
  • Mount Sinai Med Ctr
  • Stephen Hauptman

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
February 19, 2009
Sponsor
Abbott
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1. Study Identification

Unique Protocol Identification Number
NCT00002223
Brief Title
A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients
Official Title
Ritonavir (ABT-538)/Indinavir Combination Treatment in HIV-Infected Patients Previously Receiving Indinavir 800 mg TID
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Abbott

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Drug Therapy, Combination, Adolescent Behavior, HIV Protease Inhibitors, Ritonavir, Indinavir

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Indinavir sulfate
Intervention Type
Drug
Intervention Name(s)
Ritonavir

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients must have: HIV infection. CD4 cell count greater than 100 cells/microliter. HIV RNA levels greater than 400 copies/microliter using the Roche Ultrasensitive assay. No acute illness. Consent of parent or guardian if less than legal age. No prior enrollment in this study. All entry criteria for this study met within 15 days prior to enrollment. 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: Concurrent non-nucleoside reverse transcriptase inhibitors as part of the antiretroviral regimen. Any of the following medications with ritonavir: midazolam, clorazepate, diazepam, estazolam, flurazepam, triazolam, zolpidem, quinidine, amiodarone, encainide, flecainide, propafenone, bepridil, terfenadine, astemizole, cisapride, bupropion, clozapine, rifabutin, meperidine, propoxyphene, piroxicam, pimozide, dihydroergotamine, and ergotamine. Any of the following medications with indinavir: terfenadine, astemizole, cisapride, triazolam, midazolam. No requirement for rifampin or ketoconazole. Any concurrent treatment with other protease inhibitors. Other concurrent medication (including over-the-counter medicine or alcohol) without the knowledge and permission of the primary investigator. Patients with the following prior conditions are excluded: History of significant drug hypersensitivity. Psychiatric illness that precludes compliance with the protocol. Receipt of investigational drug within 30 days prior to administration of study drug. History of acute or chronic pancreatitis. Anticipation of poor patient compliance with protocol. 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.
Facility Information:
Facility Name
AIDS Healthcare Foundation
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Tower Infectious Diseases
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
Facility Name
Urgent Care Ctr / North Broward Hosp District
City
Fort Lauderdale
State/Province
Florida
ZIP/Postal Code
33316
Country
United States
Facility Name
Goodgame Med Ctr / Central Florida Research Initiati
City
Maitland
State/Province
Florida
ZIP/Postal Code
32751
Country
United States
Facility Name
Mount Sinai Med Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Stephen Hauptman
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

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A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients

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