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Completed

NCT Number: NCT00053430

Using the Drug Thalidomide to Stimulate T Cells in HIV-Infected People

Despite treatment with anti-HIV drugs, people infected with HIV continue to have problems with their immune systems. This study will evaluate whether the drug thalidomide, which stimulates the immune system's T cells, can improve immune system function in people with HIV.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Miami School of Medicine

Miami, Florida, 33125, United States

About this study

In patients with chronic HIV infection, HIV replication and abnormalities in immune function persist following treatment with highly active antiretroviral therapy (HAART). Specifically, costimulatory T cell interactions are impaired. The immune modulatory drug thalidomide was recently found to costimulate T cells. Pharmacologic T cell costimulation may compensate for the T cell deficiencies in people with HIV disease and improve immune function. This study will test whether thalidomide treatment enhances HIV and cytomegalovirus (CMV)-specific immunity in patients with HIV and CMV, and will evaluate the effect of thalidomide on HIV replication.

In this study, 40 HIV and CMV infected patients on HAART and 40 HIV uninfected CMV seropositive controls will be randomly assigned to low dose thalidomide or placebo treatment for 28 days. T cell responses and HIV replication and genetic diversification will be assessed.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV-infected for at least 5 years prior to study entry
  • CD4 count of 300/mm3 or above
  • Pre-HAART nadir CD4 count of 300/mm3 or less
  • CMV infection
  • HAART for 12 months prior to study entry
  • Same effective HAART regimen for 3 months prior to study entry
  • HIV viral load less than 200 copies/ml
  • Clinically stable

Exclusion criteria

  • Active opportunistic infection
  • Females of childbearing potential

Treatment and study plan

thalidomide

Drug

Tablet taken orally daily

Thalidomide placebo

Drug

Placebo tablet taken orally daily

Primary outcomes

  1. Doubling in HIV Pol-specific CD8 cells, measured by ELISPOT

    Time frame: Through Day 28

  2. Increase in CMV pp65 CD8 cells, measured by ELISPOT in the thalidomide treatment group

    Time frame: Throughout study

  3. Increase in HIV p24-specific IFN-gamma-secreting CD4 cells in the thalidomide treatment group, measured by fluorescence-activated cell sorting (FACS)

    Time frame: Throughout study

  4. Increase in cytomegalovirus (CMV)-specific interferon (IFN)-gamma-secreting CD4 T cells in the thalidomide treatment group, measured by FACS

    Time frame: Throughout study

Secondary outcomes

  1. Increase in the frequency of keyhole limpet hemocyanin (KLH)-specific lymphocyte proliferative responses in the thalidomide treatment group

    Time frame: Throughout study

  2. Increase in adverse events in the thalidomide treatment group

    Time frame: Throughout study

Sponsors and collaborators

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Nih

Registry information

Official study title

Pharmacologic T Cell Costimulation In HIV Disease

Important dates

Study start
2001
Primary completion
2005
Study completion
2006
First posted
Jan 30, 2003
Registry last updated
Aug 7, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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