Overview

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

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
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.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Abbott
Treatments:
Nelfinavir
Ritonavir
Criteria
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.