A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease
Information source: National Institute of Allergy and Infectious Diseases (NIAID)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: HIV Infections
Intervention: Zidovudine (Drug)
Phase: N/A
Status: Active, not recruiting
Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)
Summary
To facilitate the use of zidovudine (AZT) in children who are 3 months to 12 years of age who
are HIV-infected and either symptomatic or have a CD4 cell count < 400 cells/mm3 and to
monitor adverse effects of AZT.
Previous studies with pediatric patients have shown improvements in clinical, immunologic,
and virologic parameters with administration of AZT.
Clinical Details
Official title: A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease
Study design: Treatment
Detailed description:
Previous studies with pediatric patients have shown improvements in clinical, immunologic,
and virologic parameters with administration of AZT.
This Treatment IND (investigational new drug) is an open label, uncontrolled protocol. AZT is
ordered and prescribed by the patient's physician. The physician is responsible for obtaining
informed consent, assuring that the patient meets the eligibility criteria, dispensing the
medication to the patient, monitoring the patient's condition on treatment, and reporting
required data to the project coordinating center.
Eligibility
Minimum age: 3 Months.
Maximum age: 12 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria
Concurrent Treatment:
Allowed:
- Blood transfusions for hematologic toxicity.
Criteria for children 3 months to less than 15 months of age:
- Patient must be HIV antibody-positive by repeated reactive screening test (e. g.,
ELISA) and positive confirmatory test (e. g., Western blot).
OR
- If antibody-negative, patient must have two positive p24 antigen determinations
performed at least one week apart or have had a positive HIV culture.
Patients must meet two of the following criteria:
- Be HIV culture positive or p24 antigen positive.
- Have at least one of the Class P-2 symptoms (by CDC criteria).
Be immunosuppressed defined as having:
- CD4+(T4) lymphocytes = or < 400 cells/mm3.
- Abnormal age adjusted immunoglobulin levels (IgG or IgA). Decreased helper/suppressor
ratio < 1. 0.
Note:
- In general, abnormal values for any of the above lab tests should be confirmed in 2
measurements at least 1 week apart, and other clinical causes for these abnormalities
should be ruled out.
Criteria for children 15 months to 12 years of age:
- Patient must be HIV antibody-positive by repeated reactive screening test (e. g.,
ELISA) and positive confirmatory test (e. g., Western blot).
OR
- If antibody-negative, patient must have two positive p24 antigen determinations
performed at least one week apart or have had a positive HIV culture.
Patients must meet one of the following criteria:
- Have at least one of the class P-2 symptoms (by CDC criteria).
- Be immunosuppressed defined as having CD4+(T4) lymphocytes = or < 400 cells/mm3, based
on two measurements at least 1 week apart.
Exclusion Criteria
Co-existing Condition:
Patients with known hypersensitivity to AZT are excluded.
Patients with the following are excluded:
- Failure to meet inclusion criteria.
- Inability to obtain signed informed consent from a parent or legal guardian.
- Enrollment in another treatment protocol that expressly prohibits concomitant
treatment with zidovudine (AZT).
- Enrollment in another clinical trial in which AZT is a treatment.
- Known hypersensitivity to AZT.
Locations and Contacts
Glaxo Wellcome Inc, Research Triangle Park, North Carolina 27709, United States
Additional Information
Click here for more information about Zidovudine
Last updated: June 23, 2005
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