A Phase II Study to Evaluate the Safety, Tolerance and Efficacy of Hyperimmune Anti-HIV Intravenous Immunoglobulin (HIVIG) and of Zidovudine (ZDV) in Infants With Documented HIV Infections
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-04
112
Participants Needed
N/A
Research Sites
N/A
Total Duration
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AI-Summary
Official Title
Who Can Participate
Trial Site Locations
How is the study designed?
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Frequently Asked Questions
Research Publications
Sponsors
N
National Institute of Allergy and Infectious Diseases (NIAID)
Lead Sponsor
A
Abbott
Collaborating Sponsor
AI-Summary
What this Trial Is About
To determine the safety and tolerance of hyperimmune anti-HIV intravenous immunoglobulin (HIVIG) and of zidovudine (AZT) in infants with established HIV infection; to get preliminary evidence for the effectiveness of this type of treatment in preventing the advance of disease in HIV infected infants. HIVIG may be an effective agent that either alone or in combination with AZT will prevent progression of clinical disease.
CONDITIONS
Official Title
The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin (HVIG) Plus Zidovudine in HIV-Infected Infants
Who Can Participate
Age: 1Day - 3Months
All Genders
Eligibility Criteria
You may qualify if you...
Inclusion Criteria
Concurrent Medication:
Allowed:
Recommended:
Standard immunizations. Should repeat MMR 3 months after discontinuing study.
Benadryl and/or aspirin.
Pneumocystis carinii pneumonia prophylaxis.
Systemic ketoconazole and acyclovir, or oral nystatin for acute therapy.
Aerosol ribavirin for short-term treatment of RSV.
Concurrent Treatment:
Allowed:
Blood transfusion.
Patients must have the following:
Parent or guardian available to give written informed consent.
Protocol requires prior Institutional Review Board (IRB) approval before any subject is entered into study.
Prior Medication:
Allowed:
Gammaglobulin, intravenous (IV) or intramuscular (IM).
Immunoglobulin, IV (IVIG).
Maternal antiretroviral treatment during pregnancy.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
Symptomatic of any class P-2 symptoms (except lymphadenopathy at time of study entry.
Presence of serious acute infection requiring parenteral treatment at time of study entry.
Concurrent Medication:
Excluded:
Prophylaxis for oral candidiasis or otitis media or other infections.
Immunoglobulin therapy (except single dose or for hypogammaglobulinemia).
Ketoconazole, acyclovir, or nystatin for prophylaxis.
Patients with the following are excluded:
Symptomatic of any class P-2 symptoms (except lymphadenopathy at time of study entry.
Presence of serious acute infection requiring parenteral treatment at time of study entry.
Prior Medication:
Excluded:
Antiretroviral treatment or experimental treatment within 2 weeks of entry.
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
Trial Site Locations
Site Locations not provided
Location information for this trial is currently unavailable.
A controlled trial of intravenous immune globulin for the prevention of serious bacterial infections in children receiving zidovudine for advanced human immunodeficiency virus infection. Pediatric AIDS Clinical Trials Group.