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A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease

A Treatment IND for Retrovir Brand Zidovudine (AZT) Therapy of Pediatric Patients With HIV Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000662
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
1993-05-31
Last updated
2016-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Drugs, Investigational, Acquired Immunodeficiency Syndrome, AIDS-Related Complex, Zidovudine

Brief 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.

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.

Interventions

DRUGZidovudine

Sponsors

Glaxo Wellcome
CollaboratorINDUSTRY
National Institute of Allergy and Infectious Diseases (NIAID)
Lead SponsorNIH

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
3 Months to 12 Years
Healthy volunteers
No

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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026