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Completed

Phase 2
All Genders
ID00001282

A Phase III Study of the Combination of Azidothymidine and Interleukin-2 IL-2 in the Treatment of HIV-Infected Patients

Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2008-03-04

73

Participants Needed

1

Research Sites

N/A

Total Duration

AI-Summary

What this Trial Is About

This study will evaluate the long-term toxicity and obtain preliminary information about long-term efficacy of the combination of antiretroviral therapies and interleukin-2 (IL-2), a cytokine with immunomodulatory properties. Currently 73 patients have been approved to receive IL-2 at a starting dose of 18 MIU/d for 5 days. Multiple courses of IL-2 will be administered, at approximately 2 month intervals. Clinical, laboratory, immunologic, and viral parameters will be closely monitored during this time for evidence of toxicity and preliminary evidence of efficacy.

CONDITIONS

Brief Title

A Phase I/II Study of the Combination of Azidothymidine and Interleukin-2 (IL-2) in the Treatment of HIV-Infected Patients

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