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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 - Article


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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.

Sponsored by: Glaxo Wellcome
Information provided by: AIDS Clinical Trials Information Service

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

Further Study Details: 

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

Study ID Numbers:  264C; PROA3004
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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December 1, 2009



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