Umbrella Study for HIV Infected Adults Enrolled in NIAID-Funded Interleukin-2 Studies

Completed

• Conditions: HIV Infections
• Interventions: Drug: Interleukin-2

• Registration Number: NCT00311688
• Lead Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)

Brief Summary

Interleukin-2 (IL-2) is a protein found naturally in the blood that helps boost the immune system. The purpose of this study is to provide long-term treatment and monitoring of HIV infected people enrolled in NIAID-funded studies investigating the use of laboratory-made IL-2 for the treatment of HIV infection.

Detailed Description

IL-2 is a biological response modifier that can improve the body's response to disease. It is hoped that IL-2 treatment can help restore CD4 cell counts and immune function in people whose immune systems have been damaged by HIV. Over the last 10 years, NIAID has sponsored a number of important studies of IL-2 in HIV infected people; many of these trials are ongoing. This study was developed in an effort consolidate these separate, smaller trials into one larger study so that results between the trials can be shared and used to develop future protocols. This study is an umbrella study that will provide long-term administrative support, treatment, and monitoring for ongoing Phase I and II IL-2 trials and their participants. It is primarily intended for patients in the extension phases of any previous NIAID Clinical Center HIV Program (NIAID/CCMD) intramural research protocols in which IL-2 therapy continues to be offered. Blood collection will occur through a patient's participation in this study.

Participants will continue to follow the protocol in which they originally enrolled. A desired therapeutic goal or "CD4 plateau" will be used in most cases to help clinicians determine when a participant requires additional IL-2. In general, if a participant has two or more consecutive CD4 counts below the CD4 plateau, additional IL-2 will be administered to that patient. In maintaining uniformity among the many trials being consolidated under this trial, the frequency and nature of study visits will be solely dictated by this umbrella study. Participants will also be asked to join an optional substudy: Interrupted Versus Continuous Antiretrovirals Involving Randomization from the Umbrella Study (ICARUS).

Study Timeline

• Study Start: 2003-12
• Study First Submitted: 2006-04-04
• Study First Submitted QC: 2006-04-04
• Study First Posted: 2006-04-06
• Primary Completion: 2008-12
• Study Completion: 2008-12
• Status Verified: 2021-10
• Last Update Submitted: 2021-10-28
• Last Update Posted: 2021-11-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• HIV-1 infected
• Current participation and presently in good standing in a NIAID/CCMD clinical trial involving the use of IL-2 for the treatment of HIV-1 infection. Additional HIV-1 infected people who are IL-2 naive may be selected by the investigator for this study.
• Willing to take antiretrovirals within a 10-day period surrounding each IL-2 cycle. Individual protocols may be modified as needed by the investigator to permit IL-2 therapy in the absence of antiretrovirals.
• Willing to accept additional IL-2 therapy when needed
• Willing to use acceptable forms of contraception during a minimum 10-day period surrounding each IL-2 injection

Exclusion Criteria

• History of noncompliance with prior NIAID/CCMD protocols
• Any organic central nervous system (CNS) abnormality requiring treatment with antiseizure medication
• Unless previously exempted for this requirement, current or history of Crohn's disease, psoriasis, or other autoimmune or inflammatory disease with potentially life-threatening complications
• Significant heart, lung, kidney, rheumatologic, gastrointestinal, or CNS disease that may pose an unacceptable risk to the participant during IL-2 therapy
• Psychiatric illness that, in the opinion of the investigator, may interfere with the study
• Current or recent substance abuse that, in the opinion of the investigator, may interfere with the study
• Refuse to follow Clinical Center policy on partner notification
• History of optic neuritis
• Refuse to allow extra blood specimens to be stored for potential use in future studies of HIV-1 infection or the immune system

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
1	Interleukin-2	Individuals will follow the schedule of the study they are participating in

Primary Outcome Measures

Name	Time	Method
CD4 counts in participants treated with IL-2 and discontinued antiretroviral therapy	Throughout study

Trial Locations

Locations (1)

NIH Intramural Research Program ACTG CRS; 🇺🇸 Bethesda, Maryland, United States