AMD-3100

A Phase I/Phase II trial for HIV+ individuals, testing the safety and antiviral activity of an entry inhibitor.

 

Background

AMD-3100 belongs to a class of drug called entry (fusion) inhibitors,
and has properties that may prevent HIV from entering T-cells.
Objective
To determine whether the addition of AMD-3100 to stable antiretroviral therapy or treatment with AMD-3100 alone will prevent HIV from replicating in T-cells by blocking one of the cellular proteins to which HIV attaches. Participants will take the AMD-3100 in addition to their present antiretroviral regimens or, if not on antiretroviral therapy, as their sole investigational therapy for the duration of the study.

 

Study Design

A Phase I/Phase II dose escalation study of the safety and antiviral activity of AMD-3100 administered by continuous intravenous infusion to volunteers infected with HIV-1. This is a 12-day, in-patient study. Participants will be compensated up to $1200.
Inclusion
Criteria
  • HIV+ man or woman, at least 18 years old
  • Individuals on stable antiretroviral therapy.
  • Individuals on no antiretroviral therapy.
  • Must have type of HIV called "Syncytium-Inducing" (SI)�ARA will test for this and cover the cost)
  • Viral load greater or equal to 5000 copies.
  • T-cell count greater than or equal to 10.
  • Woman who are not pregnant and are willing to use contraceptives for the duration of the study

Status
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Enrolling
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For more information about participating in this study in the Los Angeles area, please call 310/358.2429 or e-mail Corie Castro at ccastro@aidsresearch.org

We encourage participation by women and people of color.

This ad was reviewed and approved by the AIDS Research Alliance Institutional Review Board on August 15, 2000.

 


 

 

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