NCT Number: NCT00000789
A Randomized, Comparative Trial of Zidovudine (AZT) Versus 2',3'-Didehydro-3'-Deoxythymidine (Stavudine; d4T) in Children With HIV Infection
PRIMARY: To compare the relative safety and tolerance of oral zidovudine (AZT) versus oral stavudine (d4T) in symptomatic HIV-infected children.
SECONDARY: To compare the clinical, virologic, and immunologic responses between the two treatment groups, and to obtain pharmacokinetic data for both drugs.
At present, AZT is considered the drug of choice for initial treatment of most children with HIV infection, although disease progression or drug intolerance is associated with its long-term use. In preliminary studies in children, d4T, another HIV inhibitor, has been well tolerated, although an optimum dose has not been determined.
Looking for future studies?
Notify MeKey information
Conditions
Age range
3 month–6 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Univ. Hosp. Ramón Ruiz Arnau, Dept. of Peds., Bayamón, Puerto Rico
About this study
At present, AZT is considered the drug of choice for initial treatment of most children with HIV infection, although disease progression or drug intolerance is associated with its long-term use. In preliminary studies in children, d4T, another HIV inhibitor, has been well tolerated, although an optimum dose has not been determined.
Patients are randomized to receive either oral AZT or oral d4T. Treatment continues until the last patient enrolled has received 52 weeks of therapy, or until the study is terminated.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Recommended:
- PCP prophylaxis.
Allowed:
- Immunoglobulin.
- Erythropoietin, G-CSF, and GM-CSF.
- Corticosteroids.
- Ethionamide or isoniazid for TB if no alternative is available.
- Pyridoxine (up to 50 mg/day) as vitamin supplement.
Patients must have:
- Symptomatic HIV infection.
- No more than 6 weeks of prior antiretroviral or immunomodulator therapy (other than steroids and IVIG).
- Consent of parent or guardian.
NOTE:
- Coenrollment on another ACTG protocol not involving antiretroviral therapy is permitted.
Prior Medication:
Allowed:
- Maternal immunomodulator or antiretroviral therapy (including during pregnancy).
- Antiretroviral therapy prior to 2 months.
- Up to 6 weeks of prior antiretroviral therapy or specific immunomodulator therapy (other than corticosteroids and IVIG).
Exclusion criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Current grade 3 or worse neuropathy / lower motor neuropathy.
- Other grade 3 or worse clinical or laboratory toxicities.
- Known intolerance to either AZT or d4T.
Concurrent Medication:
Excluded:
- Chemotherapy for active malignancy.
Patients with the following prior conditions are excluded:
- History of grade 3 or worse neuropathy/lower motor neuropathy.
Prior Medication:
Excluded:
- More than 6 weeks of prior antiretroviral or immunomodulator therapy.
- Antiretroviral or immunomodulator therapy within 7 days prior to study entry. Ongoing drug or alcohol abuse.
Treatment and study plan
Zidovudine
DrugSponsors and collaborators
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
Collaborators
- Bristol-Myers Squibb
- Glaxo Wellcome
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.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Randomized, Phase I/II, Dose-Ranging, Open-Label Trial of the Anti-HIV Activity of Delavirdine Mesylate (DLV; U-90,152S)
NCT00000810
AIDS-Related Complex, Acquired Immunodeficiency Syndrome
Stanford, California, United States
View Trial DetailsA Phase II, Double-Blind Trial of Recombinant Human Nerve Growth Factor for Treatment of HIV-Associated Sensory Neuropathy
NCT00000842
AIDS-Related Complex, Acquired Immunodeficiency Syndrome
Los Angeles, California, United States
View Trial DetailsA Phase I/II Study of Delayed-Type Hypersensitivity (DTH) Reactions to Intradermal HIV Envelope Antigen
NCT00000782
AIDS-Related Complex, Acquired Immunodeficiency Syndrome
Palo Alto, California, United States
View Trial DetailsComparison of Two Dosage Regimens of Oral Dapsone for Prophylaxis of Pneumocystis Carinii Pneumonia in Pediatric HIV Infection
NCT00000739
AIDS-Related Complex, Acquired Immunodeficiency Syndrome
Long Beach, California, United States
View Trial Details