Safety and efficacy of polyethylene glycol-modified interleukin-2 and zidovudine in human immunodeficiency virus type 1 infection: a phase I/II study.
R Wood, J G Montoya, S K Kundu...
https://pubmed.ncbi.nlm.nih.gov/8095058Completed
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2008-08-04
26
Participants Needed
1
Research Sites
N/A
Total Duration
To determine the safety of polyethylene glycolated IL-2 (PEG IL2) administered weekly or biweekly (per amendment) in a setting of oral zidovudine (AZT). To determine the effect of PEG IL2 in combination with AZT on parameters assessing the immune system as well as HIV virus and antibody titers. To evaluate a chronic dosing study phase offered to patients who complete the initial 25-week regimen. Recent research has focused on enhancing cell-mediated immunity and reducing or eliminating viral replication (reproduction and growth). A main thrust of current treatment is the combination of antiviral drugs that may be more effective when combined than when each is used alone.
CONDITIONS
Safety and Efficacy of Polyethylene Glycolated IL-2 (PEG IL-2) Plus Zidovudine in HIV Positive, Asymptomatic and Symptomatic Individuals
You may qualify if you...
Inclusion Criteria
Concurrent Medication:
Allowed:
Patients must:
Allowed:
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
Concurrent Medication:
Excluded:
Concurrent Treatment:
Excluded:
Patients with the following are excluded:
Prior Medication:
Excluded within 30 days prior to study entry:
Prior Treatment:
Excluded within 30 days prior to study entry:
Excluded within 4 weeks prior to study entry:
Active substance abuse.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Total: 1 location
1
Stanford Univ School of Medicine
Stanford, California, United States, 94305
Status Unknown
Study Type
INTERVENTIONAL
Masking
N/A
Allocation
N/A
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
0
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R Wood, J G Montoya, S K Kundu...
https://pubmed.ncbi.nlm.nih.gov/8095058