(RITA!) HIV Treatment Alerts - September 2002
Immune restoration study
One of the challenges in HIV medicine is to try to restore the immune system to a healthier state after it has been attacked by HIV. Combination HIV therapy helps, but the restoration is still incomplete. Doctors from the AIDS Clinical Trials Unit (ACTU) at The University of Texas Medical Branch (UTMB) in Galveston are trying to find ways to improve immune restoration. In their study, they will use an experimental AIDS vaccine, interleukin-2 (an immune booster), and HIV treatment interruptions to see if immune restoration can be improved. To be eligible, patients must have been receiving combination anti-HIV therapy (3 or more drugs) for longer than 6 months; Ziagen (which is present in Trizivir) cannot be one of the drugs used. Also required are a T cell count greater than 350 and viral load less than 50, no previous or current AIDS-defining illness (except Kaposi's Sarcoma if less than 5 skin lesions), and no use of an HIV vaccine within the past year. For more information, contact the ACTU at 409.772.3991 or toll free at 877.324.2288. More information about the ACTU research group can be found on the Web at http://actu.utmb.edu/actu.
Study to test safety and anti-HIV effectiveness of potential drug
An experimental nucleoside reverse transcriptase inhibitor (NRTI) called "ACH-126,443" is being tested for safety and anti-HIV effectiveness. This drug is in the same family as drugs like Epivir, Zerit, Videx, and Retrovir. The study (called "Achillion 006") will look at 3 groups of patients, where one group stays on Epivir, but the other groups switch Epivir for ACH-126,443 at either of 2 doses. The patients will be followed in the study for 4 weeks. Although this study does not have much advantage for treatment-experienced patients who need new treatment options, it is a preliminary and necessary step to move the drug forward into longer, more in-depth study. Entry criteria for this study include being on an Epivir-containing drug regimen, experiencing viral rebound after previous HIV suppression (current viral load between 1000 and 30,000), having T cells greater than 200, and
test results showing viral resistance to Epivir. Also, patients must be older than 18 years, cannot be pregnant or breast-feeding, and cannot have any opportunistic infections or hepatitis B or C infection. The study is enrolling locally at Houston's Montrose Clinic. For more information, contact Rick Witt, PA-C, at 713.830.3013.
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Copyright © 2002 - Research Initiative Treatment Action (RITA!). Reproduced with permission. RITA! is published by The Center for AIDS. Contact Thomas Gegeny, MS, ELS, Editor, RITA! for permission to reproduce RITA!. tom@centerforaids.org. http://www.centerforaids.org
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