Completed

Phase Not Applicable
Age: 16Years +
All Genders
ID00001075

A Pilot Study to Evaluate the Immunologic Consequences of a Highly Active Antiretroviral Therapy Regimen (HAART) Consisting of Ritonavir (ABT-538), Zidovudine (AZT), and Lamivudine (3TC) in Moderately Advanced HIV-1 Disease

Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-04

55

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

To determine whether administration of a highly active antiretroviral treatment regimen consisting of ritonavir (ABT-538), zidovudine (AZT), and lamivudine (3TC) is associated with the restoration of delayed type hypersensitivity and lymphocyte proliferative responses in patients with moderately advanced HIV-1 infection. To better characterize in these patients the phenotype of the expanded lymphocyte subpopulations, as well as the genotype, phenotype, and cellular origin of viruses that persist after initiation of therapy, and the genotype and phenotype of drug-resistant isolates that emerge during therapy. Although plasma viral load drops dramatically after initiation of powerful antiretrovirals, it does not drop to zero. It appears that a new steady state is reached, suggesting that a reservoir may exist of virus-producing cells, possibly cells of monocyte/macrophage lineage, that continue to produce a low level of virus despite antiretroviral treatment.

CONDITIONS

Official Title

The Effectiveness of Ritonavir Plus Zidovudine Plus Lamivudine in HIV-Infected Patients

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

Inclusion Criteria

Concurrent Medication:

Allowed:

  • Recombinant erythropoietin and/or G-CSF for AZT-related bone marrow suppression.
  • Antibiotics other than metronidazole.
  • PCP prophylaxis.
  • Regularly prescribed medications such as antipyretics, analgesics, allergy medicine, and oral contraceptives.
  • Vitamins and herbal therapies.

Concurrent Treatment:

Allowed:

  • Acupuncture.
  • Visualization techniques.

Patients must have:

  • Documented HIV infection.
  • CD4 count 100-300 cells/mm3.
  • At least 3 consecutive months of prior AZT at a dosage of 500-600 mg bid, but with 5 weeks of antiretroviral washout prior to study entry.
  • Consent of parent or guardian if less than 18 years old.

Prior Medication:

Required:

  • Prior AZT at 500-600 mg bid at any time.
  • PCP prophylaxis during antiretroviral washout.

Allowed:

  • Prior ddI and/or ddC.
  • Prior recombinant erythropoietin and/or G-CSF for AZT-related bone marrow suppression.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Chronic pancreatitis.
  • Psychological conditions that would affect compliance.
  • Intolerance to 500-600 mg/day AZT.
  • Concurrent participation on another antiretroviral research treatment study (study treatment for opportunistic infection or complications of HIV is allowed).
  • Considered likely to be noncompliant on study.

Concurrent Medication:

Excluded:

  • Immunomodulators such as systemic corticosteroids, thalidomide, or cytokines.
  • Rifabutin.
  • Disulfiram (Antabuse) or other medications with similar effects, including metronidazole.
  • Other drugs contraindicated with ritonavir.

[AS PER AMENDMENT 8/27/96: Immunization must be avoided during the antiretroviral washout period.]

Patients with the following prior conditions are excluded:

  • Active opportunistic infection or febrile illness with temperature >= 38.5 C within 3 days prior to study entry.
  • History of acute pancreatitis within the past 2 years.

Prior Medication:

Excluded:

  • Prior 3TC or a protease inhibitor.
  • Experimental drugs except those for HIV-related conditions, within the past 30 days.

[AS PER AMENDMENT 8/27/96: Immunization must be avoided prior to the antiretroviral washout period.]

Active substance abuse.

Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Total: 3 locations

1

University of Colorado Hospital CRS

Aurora, Colorado, United States, 80045

Status Unknown

2

Rush Univ. Med. Ctr. ACTG CRS

Chicago, Illinois, United States, 60612

Status Unknown

3

Case CRS

Cleveland, Ohio, United States, 44106

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial

Immunologic responses associated with 12 weeks of combination antiretroviral therapy consisting of zidovudine, lamivudine, and ritonavir: results of AIDS Clinical Trials Group Protocol 315.

M M Lederman, E Connick, A Landay...

https://pubmed.ncbi.nlm.nih.gov/9652425

Increases in T cell telomere length in HIV infection after antiretroviral combination therapy for HIV-1 infection implicate distinct population dynamics in CD4+ and CD8+ T cells.

S Kaushal, A L Landay, M M Lederman...

https://pubmed.ncbi.nlm.nih.gov/10413649

Effect of zidovudine resistance mutations on virologic response to treatment with zidovudine-lamivudine-ritonavir: genotypic analysis of human immunodeficiency virus type 1 isolates from AIDS clinical trials group protocol 315.ACTG Protocol 315 Team.

D R Kuritzkes, A Sevin, B Young...

https://pubmed.ncbi.nlm.nih.gov/10669331

Multiple CD4+ cell kinetic patterns and their relationships with baseline factors and virological responses in HIV type 1 patients receiving highly active antiretroviral therapy.

H Wu, E Connick, D R Kuritzkes...

https://pubmed.ncbi.nlm.nih.gov/11559422

Characterization of viral dynamics in human immunodeficiency virus type 1-infected patients treated with combination antiretroviral therapy: relationships to host factors, cellular restoration, and virologic end points.

H Wu, D R Kuritzkes, D R McClernon...

https://pubmed.ncbi.nlm.nih.gov/10068574
A Pilot Study to Evaluate the Immunologic Consequences of a Highly Active Antiretroviral Therapy Regimen (HAART) Consisting of Ritonavir (ABT-538), Zidovudine (AZT), and Lamivudine (3TC) in Moderately Advanced HIV-1 Disease | DecenTrialz