Nucleoside Analogues |
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Clinical Trial: Safety and Effectiveness of Giving Two Nucleoside Reverse Transcriptase Inhibitors Alone or in Combination with 141W94 to HIV-Infected Children Who Have Never Received Protease Inhibitors
This study has been completed.
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Purpose
The purpose of this study is to see if it is safe and effective to add a new protease inhibitor (PI), 141W94, to an anti-HIV regimen that includes 2 nucleoside reverse transcriptase inhibitors (NRTIs).
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| HIV Infections | Drug: Amprenavir | Phase III |
MedlinePlus related topics: AIDS
Study Type: Interventional
Study Design: Treatment, Parallel Assignment, Safety Study
Official Title: A Randomized, Double-Blind, Placebo-Controlled Phase III Study to Evaluate the Safety and Efficacy of 141W94 Plus Current Nucleoside Therapy versus Current Nucleoside Therapy Alone in Protease-Naive, HIV-Infected Children
Expected Total Enrollment: 210
In this double-blind, placebo-controlled, pediatric study, 210 patients are randomized to receive 2 NRTIs plus either 141W94 or placebo. Enrollment of patients is sequential: patients 13 to 18 years of age are enrolled first, followed by children < 13 when the appropriate pediatric dose has been determined. Patients who are unable to swallow capsules will be accrued when a liquid formulation becomes available.
Eligibility
Ages Eligible for Study: 6 Months - 18 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria
Your child may be eligible for this study if he/she:
- Is 6 months - 18 years of age.
- Is HIV-positive.
- Has a viral load (level of HIV in the body) greater than 10,000 copies/ml.
- Is able to take medications by mouth.
- Has consent of parent or legal guardian if under 18.
- Has a negative pregnancy test within 7 days of study entry.
- Agrees to practice abstinence or use effective methods of birth control for 1 month before and throughout the study.
Exclusion Criteria
Your child will not be eligible for this study if he/she:
- Has a serious illness, including any life-threatening infection or other chronic serious medical condition.
- Has an opportunistic (AIDS-related) infection or a serious bacterial infection.
- Is allergic to NRTIs.
- Is breast-feeding.
- Is unlikely to complete the study.
- Has received certain medications.
- Has received radiation therapy within the past 4 months, or will need to receive it during the study.
Location Information
Florida
Children's Diagnostic Treatment Ctr, Fort Lauderdale, Florida, 33301, United States
Tennessee
Saint Jude Children's Hosp / Dept of Infect Diseases, Memphis, Tennessee, 38105, United States
More Information
Record last reviewed: June 1999
Last Updated: October 13, 2004
Record first received: November 2, 1999
ClinicalTrials.gov Identifier: NCT00002193
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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