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A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patients

Safety and Efficacy of Ritonavir (ABT-538) in Combination With Nelfinavir in HIV-Infected Subjects.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002201
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2009-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Drug Therapy, Combination, HIV Protease Inhibitors, Ritonavir, Nelfinavir, Anti-HIV Agents

Brief summary

The purpose of this study is to see if it is safe and effective to give ritonavir plus nelfinavir to HIV-infected patients. This study will also see how ritonavir and nelfinavir are absorbed by the body and how they affect the level of HIV in the blood.

Interventions

DRUGRitonavir
DRUGNelfinavir mesylate

Sponsors

Abbott
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have: * Documentation of a positive ELISA test for HIV confirmed by immunoblot, or a positive HIV RNA test using the Roche PCR assay, or the Chiron bDNA assay. * HIV RNA measurement of \> 5,000 copies/ml within 3 weeks of baseline visit. * Signed, informed consent from parent or legal guardian for patients less than 18 years of age. * Access to a refrigerator for storing study drug. Prior Medication: Allowed: Anti-HIV therapy other than protease inhibitor therapy.

Exclusion criteria

Co-existing Condition: Patients with the following conditions or symptoms are excluded: * Evidence of acute infection, as measured by vital signs, physical examination, 12-lead electrocardiogram and laboratory assessments. * Condition that may obscure the proper observation of the safety or activity of the treatment regimens. Concurrent Medication: Excluded: * Midazolam, alprazolam, clorazepate, diazepam, estazolam, flurazepam, triazolam, zolpidem, quinidine, amiodarone, encainide, flecainide, propafenone, bepridil, terfenadine, astemizole, cisapride, bupropion, clozapine, rifabutin, meperidine, propoxyphene, piroxicam, pimozide, ergotamine, dihydroergotamine, and rifampin. * Anti-retroviral therapy initiated prior to study entry. * Any other medication, including over-the-counter medicine and alcohol, taken without the permission of the primary investigator. Patients with the following prior conditions are excluded: * History of significant drug hypersensitivity. * History of psychiatric illness that would preclude compliance with the protocol. * Prior enrollment in this study. Prior Medication: Excluded: * Investigational drugs within 30 days prior to drug administration. * Prior treatment with licensed or investigational HIV protease inhibitor. 1\. Active substance abuse. * Positive urine screen for recreational drugs. NOTE: * The presence of cannabis is not exclusionary unless the investigator believes its use will interfere with patient compliance.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026