NCT Number: NCT00000827
A Phase I/II Study of Hyperimmune IVIG in Slowing Progression of Disease in HIV-Infected Children
To evaluate the safety, tolerance, pharmacokinetics, and antiviral activity of human anti-HIV immune serum globulin ( HIVIG ) at three dosage levels in HIV-infected children.
Passive antibody therapy has been used with limited success in treating advanced HIV disease in adults. HIVIG is manufactured from HIV antibody-rich plasma taken from asymptomatic donors. It is hypothesized that HIVIG will decrease the viral burden of moderately advanced HIV-positive children.
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Conditions
Age range
2 year–12 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
San Juan City Hosp. PR NICHD CRS, San Juan, Puerto Rico
About this study
Passive antibody therapy has been used with limited success in treating advanced HIV disease in adults. HIVIG is manufactured from HIV antibody-rich plasma taken from asymptomatic donors. It is hypothesized that HIVIG will decrease the viral burden of moderately advanced HIV-positive children.
Children are randomized to receive HIVIG every 4 weeks for 6 months at one of three dose levels, then are followed for 3 months after the final infusion.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Required:
- PCP prophylaxis according to CDC guidelines.
Allowed:
- Varicella-zoster immunoglobulin.
- Hepatitis B immunoglobulin.
- Prophylactic therapies not involving immunoglobulin.
Patients must have:
- HIV infection.
- CD4 count > 200 cells/mm3 (ages 2-5 years) or > 100 cells/mm3 (age > 5 years).
- Antiretroviral therapy for at least 6 months, with no change in regimen for at least 3 months prior to study entry.
- Plasma ICD p24 >= 70 pg/ml that is stable or increasing prior to study entry.
- Life expectancy of at least 6 months.
Prior Medication: Required:
- Antiretroviral therapy for at least 6 months, with stable dose for at least 3 months.
Exclusion criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Severe diarrhea, nephrotic syndrome, or other protein-losing state that requires large doses of IVIG.
- Any other condition requiring dosing with IVIG (e.g., ITP, hypogammaglobulinemia).
- Acute illness with temperature >= 100 F and/or with IV antibiotics.
- Grade 3 or worse clinical toxicities.
- Unable to tolerate IV infusions at a minimum rate of 0.02 ml/kg/min.
- Concomitant participation in an experimental antiretroviral or HIV vaccine trial.
Concurrent Medication:
Excluded:
- IVIG.
- Chemotherapy for an active malignancy.
- MMR or rubella vaccinations.
- Intramuscular immunoglobulin.
Patients with the following prior condition are excluded:
- History of severe reaction to IVIG.
Prior Medication:
Excluded:
- IVIG within the past 60 days.
- Chemotherapy for an active malignancy within the past year.
- MMR or rubella vaccinations within the past 6 months.
- Intramuscular immunoglobulin within the past 60 days.
Ongoing drug or alcohol abuse.
Treatment and study plan
Sponsors and collaborators
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
Collaborators
- North American Biologicals Inc
Registry information
Important dates
- Study completion
- 1998
- First posted
- Aug 31, 2001
- Registry last updated
- Nov 4, 2021
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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