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Equivalence of Boosted Atazanavir Based Regimens and Currently Effective HAART Regimens

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ClinicalTrials.gov Identifier: NCT00940771
Recruitment Status : Unknown
Verified October 2015 by Janice Piatt, Phoenix Children's Hospital.
Recruitment status was:  Active, not recruiting
First Posted : July 16, 2009
Last Update Posted : October 22, 2015
Bristol-Myers Squibb
Information provided by (Responsible Party):
Janice Piatt, Phoenix Children's Hospital

July 15, 2009
July 16, 2009
October 22, 2015
April 2009
December 2016   (Final data collection date for primary outcome measure)
  • Viral Load [ Time Frame: 6 months ]
  • CD4 Count [ Time Frame: 6 months ]
Same as current
Complete list of historical versions of study NCT00940771 on ClinicalTrials.gov Archive Site
  • Non-fasting cholesterol [ Time Frame: 6 months ]
  • Non-fasting triglycerides [ Time Frame: 6 months ]
Same as current
Not Provided
Not Provided
Equivalence of Boosted Atazanavir Based Regimens and Currently Effective HAART Regimens
Equivalence of Boosted Atazanavir Based Regimens and Currently Effective HAART Regimens With Other PI's/NNRTI's in HIV+ Children and Adolescents With Elevated Lipid Levels
The hypothesis for this study is will a treatment regimen containing Atazanavir in combination with Ritonavir work as well as other regimens containing a protease inhibitor (PI, one of 5 classes of HIV Medications) and/or a Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI, another of the classes of HIV medications) at controlling HIV disease in children who are HIV+ and have high cholesterol or high triglycerides. . In this study, children who have high cholesterol or high triglycerides as a result of their HIV medicines, will have the PI or NNRTI in their medication regimen changed to Atazanavir, which is a PI in combination with a low dose of Ritonavir (another PI). Atazanavir has been shown in adults to result in lower cholesterol and triglycerides than other PI's and NNRTI's. The dose of atazanavir and ritonavir will be according to the Package Insert for this drug that is FDA approved for children. They will continue taking the other medications from the pre-study regimen. Children will take study drug for 24 weeks, and will be able to continue study drug after the study using commercially available drug. Lab tests and a physical exam will be undertaken at 4 weeks, 12 weeks and 24 weeks after starting study drug to determine how effective the new drug is and to monitor for possible side effects.

The objectives of this study are to see if Atazanavir and Ritonavir together will be as effective as the child's previous regimen in keeping the level of virus in the blood stream at such a low level it can't be found and will that combination be as effective as the previous regimen in keeping the infection fighting cells in the blood at the same level.

  • To see if cholesterol and triglyceride levels drop in children switching to Atazanavir and Ritonavir from other medication regimens.
  • To see if Atazanavir and Ritonavir result in an increase in patient satisfaction and patient reported adherence and a decrease in symptoms related to medication side effects.

Inclusion Criteria are:

  • On the same medication regimen at least 3 months
  • Weight equal to or greater than 25kg
  • Able to swallow pills or willing to learn
  • Have a parent or guardian willing and able to sign informed consent
  • Not be taking a medication which interacts with Atazanavir
  • Not be currently taking sustiva
Phase 4
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Pediatric HIV
  • HIV Infections
Drug: Boosted Atazanavir
Boosted atazanavir, once a day dose adjusted for child's weight for 6 months.
Other Name: Reyataz
Experimental: boosted atazanavir
Intervention: Drug: Boosted Atazanavir
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
Unknown status
December 2016
December 2016   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • HIV positive children with elevated lipid levels
  • on stable HAART for at least 3 months (defined to be on the same regimen with viral load < 1000 for 6 months prior to baseline visit).
  • Weight equal to or greater than 25kg
  • Able to swallow pills or willing to learn

Exclusion Criteria:

  • Patients with underlying hepatitis B or C viral infections
  • Previously demonstrated clinically significant hypersensitivity (eg, Stevens-Johnson syndrome, erythema multiforme, or toxic skin eruptions) to any of the components of Reyataz® (atazanavir).
  • Taking other medications that are highly dependent on CYP3A or UGT1A1 for clearance

    • Ergot medicines: dihydroergotamine, ergonovine, ergotamine, and methylergonovine such as Cafergot®, Migranal®, D.H.E. 45®, ergotrate maleate, Methergine®, and others (used for migraine headaches).
    • Orap® (pimozide, used for Tourette's disorder).
    • Propulsid® (cisapride, used for certain stomach problems).
    • Triazolam, also known as Halcion® (used for insomnia).
    • Midazolam, also known as Versed® (used for sedation), when taken by mouth.
    • Camptosar® (irinotecan, used for cancer).
    • Crixivan® (indinavir, used for HIV infection).
    • Cholesterol-lowering medicines Mevacor® (lovastatin) or Zocor® (simvastatin).
    • Rifampin (also known as Rimactane®, Rifadin®, Rifater®, or Rifamate®).
    • St. John's wort (Hypericum perforatum), an herbal product sold as a dietary supplement,
    • Viramune® (nevirapine, used for HIV infection).
    • Vfend® (voriconazole).
  • Patients with grade 3 or higher elevations in transaminases (> 10 X ULN)
  • Women of Childbearing Potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period.
  • Women who are pregnant or breastfeeding.
  • Women with a positive pregnancy test.
Sexes Eligible for Study: All
6 Years to 18 Years   (Child, Adult)
Contact information is only displayed when the study is recruiting subjects
United States
PCH 09-004
Not Provided
Not Provided
Janice Piatt, Phoenix Children's Hospital
Phoenix Children's Hospital
Bristol-Myers Squibb
Principal Investigator: Janice Piatt, MD Phoenix Children's Hospital
Phoenix Children's Hospital
October 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP