Safety and Effectiveness of Adding Adefovir Dipivoxil and Nelfinavir to the Anti-HIV Therapy of HIV-Infected Children

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Gilead Sciences

Status and phase

Unknown
Phase 2

Conditions

HIV Infections

Treatments

Drug: Adefovir dipivoxil
Drug: Nelfinavir mesylate
Drug: Levocarnitine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00002219
232H
GS-97-418

Details and patient eligibility

About

The purpose of this study is to see if it is safe and effective to give adefovir (a new anti-HIV drug) plus nelfinavir to HIV-infected children who are already receiving other anti-HIV medications.

Full description

During the first phase of the study (Days 1-6), the safety and tolerability of multiple doses of ADF is assessed when administered simultaneously with the patient's reverse transcriptase inhibitor (RTI) regimen. The second phase begins on Day 7 when nelfinavir is added to the therapy regimen for an additional 15 weeks. ADF pharmacokinetics are measured on Days 1, 2, and 7 (on a subset of 18 patients); peak and trough samples are collected on Day 28.

Sex

All

Ages

3 months to 16 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

Your child may be eligible for this study if he/she:

  • Is 3 months to 16 years old.
  • Is HIV-positive.
  • Has never taken protease inhibitors or has previously taken ritonavir (RTV), saquinavir (SQV), or indinavir (IDV) and is willing to stop the medication at study entry.
  • Is taking an anti-HIV drug combination that will not change during at least the 2 weeks prior to study entry.
  • Agrees to use effective barrier methods of birth control, such as condoms, during the study.
  • Has consent of parent or guardian.

Exclusion Criteria

Your child will not be eligible for this study if he/she:

  • Has ever taken NFV.
  • Has a history of opportunistic (AIDS-related) infection.
  • Has any disease or illness that would prevent him/her from completing the study, including cancer.
  • Has taken certain medications, including protease inhibitors at study entry.
  • Is receiving an HIV vaccine at study entry.
  • Is pregnant.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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