HIV Infections
Conditions
Keywords
Treatment Experienced, Treatment Interruption, Treatment Naive
Brief summary
Recombinant interferon (IFN) may be useful in the treatment of HIV. However, the high doses of IFN necessary to keep HIV under control limit its use due to toxic side effects. The purpose of this study is to test the safety and tolerability of weekly recombinant pegylated interferon (PEG-IFN) alfa-2a in HIV infected people who are currently on antiretroviral therapy (ART) interruption or who have not started taking anti-HIV drugs.
Detailed description
IFN is an immune response enhancer and is produced in the body in response to viral infection. PEG-IFN may have less harmful side effects than non-pegylated IFN. Recombinant PEG-IFN alfa-2a is a synthetic version of IFN and is used in hepatitis C virus treatment. PEG-IFN alfa-2a has demonstrated potentially useful antiviral properties in HIV treatment; however, due to the high doses that must be administered to maintain viral suppression, toxicity (especially to the blood) is a concern. This study will evaluate the safety, tolerability, and antiretroviral activity of PEG-IFN alfa-2a in HIV infected patients who have received ART in the past but are currently off ART or who are ART naive. The study will last 18 weeks. Participants will receive weekly injections of 180 mcg PEG-IFN alfa-2a at the clinic for 12 weeks. After Week 12, participants will be followed off-treatment until Week 18. Physical exams will be performed weekly. Blood collection to monitor viral load, PEG-IFN alfa-2a serum levels, and CD4 and CD8 counts will be conducted at selected weeks during the study. Filgrastim will be given to patients who exhibit neutropenic toxicity.
Interventions
DRUGPegylated interferon alfa-2a
Recombinant PEG-IFN alfa-2a is a synthetic version of IFN and is used in hepatitis C virus treatment
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* HIV infected * CD4 count of 300 cells/ml or greater within 30 days of study entry * HIV viral load of 5000 copies/ml or greater within 30 days of study entry * Received ART previously but have currently interrupted treatment within 12 weeks prior to study entry OR ART naive * Willing to delay initiation or re-initiation of antiretroviral medications for the duration of the study * Agree to use acceptable forms of contraception
Exclusion criteria
* Previous use of interferon alfa * Known allergy or sensitivity to PEG-IFN alfa-2a or its formulation * Active drug or alcohol abuse that would interfere with the study * Acute therapy for a serious infection within 30 days of study entry * Use of non-protocol-specified immunomodulatory therapy within 60 days of study entry * Active immunization within 30 days of study entry * History of severe psychiatric disease such as major depression, suicidal attempt, hospitalization for psychiatric disease, or a period of disability due to psychiatric disease * History of poorly controlled thyroid disease, including history of elevated thyroid stimulating hormone (TSH) levels with elevated antibodies to thyroid peroxidase and any clinical manifestations of thyroid disease * History of clinically significant heart disease that could be worsened by acute anemia * History of severe seizure disorder or current anticonvulsant use * Hepatitis C antibody positive within 60 days prior to study entry * Hepatitis B surface antigen positive within 60 days prior to study entry * Known sensitivity to E. coli derived products, such as filgrastim * Any past evidence of chronic liver disease * Any past or current evidence of immunologically-mediated disease * Evidence of chronic pulmonary disease * Severe eye problems due to diabetes, hypertension, cytomegalovirus infection, or macular degeneration * History of major organ transplantation with an existing functional graft * History or other evidence of severe illness, cancer, or other conditions that would make the patient unsuitable for the study * Hemoglobin abnormalities or any other cause of or tendency for breakdown of red blood cells * Any medical condition that would prevent successful completion of the study * Use of certain medications * Pregnant or breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Laboratory and clinical adverse effects | Throughout study |
| CD4 count | Throughout study |
| CD8 count | Throughout study |
Countries
United States
Outcome results
None listed