Differences in Malaria Infection Levels in HIV-infected Infants and Children Receiving PI- and NNRTI-based HAART
Primary Purpose
HIV Infections, Malaria
Status
Completed
Phase
Early Phase 1
Locations
International
Study Type
Interventional
Intervention
Lamivudine
Lopinavir/Ritonavir
Nevirapine
Zidovudine
Sponsored by
About this trial
This is an interventional treatment trial for HIV Infections focused on measuring Coinfection
Eligibility Criteria
Inclusion Criteria:
- Enrolling in study IMPAACT P1060
- Parent/legal guardian agrees to seek medical care for intercurrent illness at the study site, whenever possible, and agree to not use at-home remedies for febrile illness in the child
Exclusion Criteria:
None.
Sites / Locations
- University of North Carolina Lilongwe (12001)
- Makerere University - JHU Research Collaboration (30293)
- George Clinic CRS (30273)
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
Previously received single-dose nevirapine (SD NVP); assigned to receive either an NNRTI- or PI-based regimen as a part of the study IMPAACT P1060
Have not previously received SD NVP; assigned to receive either an NNRTI- or PI-based regimen as a part of the study IMPAACT P1060
Outcomes
Primary Outcome Measures
Parasitemia in blood samples
Secondary Outcome Measures
Time of initiation of treatment for clinical malaria requiring conventional anti-malarial therapy
Severity of malarial disease
Measured anti-malaria IgG, protein in plasma, and mRNA transcripts in PBMC of chemokines
IL4-589C/T genotypes
Full Information
NCT ID
NCT00719602
First Posted
July 17, 2008
Last Updated
September 16, 2016
Sponsor
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
1. Study Identification
Unique Protocol Identification Number
NCT00719602
Brief Title
Differences in Malaria Infection Levels in HIV-infected Infants and Children Receiving PI- and NNRTI-based HAART
Official Title
P1060 Substudy Comparing Differences in Malaria Parasitemia by Real Time Quantitative PCR in HIV-Infected Infants and Children on PI-Based HAART Versus NNRTI-Based HAART
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
August 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
More than 1.5 million deaths of African children under 5 years of age have been due to Plasmodium falciparum malaria. When HIV and malaria are present as coinfections, they enhance each other's progression. The primary purpose of this study is to compare the malarial infection levels in HIV-infected infants and children receiving protease inhibitor (PI)- or non-nucleotide reverse transcriptase inhibitor (NNRTI)-based highly active antiretroviral therapy (HAART).
Detailed Description
The World Health Organization (WHO) reports 1 to 2 million malaria deaths annually, with most malaria-related deaths occurring in children. The malaria burden is compounded by the HIV epidemic, which is most prevalent in areas endemic for malaria, notably Sub-Saharan Africa where nine in ten children younger than 15 years of age are infected with HIV. The purpose of this study is to compare parasitemia levels in HIV-infected infants and children receiving PI- or NNRTI-based HAART regimens.
This study will enroll a total of 140 participants, 35 from each of the 4 groups in IMPAACT P1060.
This substudy will last until 24 weeks after the last P1060 enrollment or until P1060 study discontinuation. Participants must meet enrollment criteria for P1060 as well as additional criteria for this study. Study visits will occur as a part of P1060 study visits, all of which include a physical exam, blood collection, and assessments of HIV-related symptoms.
Participants are also encouraged to return to the primary clinic site for intercurrent illness visits for assessment, thick and thin blood smear, and filter paper blood collection, however these visits are not mandatory for study participation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Malaria
Keywords
Coinfection
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
105 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Previously received single-dose nevirapine (SD NVP); assigned to receive either an NNRTI- or PI-based regimen as a part of the study IMPAACT P1060
Arm Title
2
Arm Type
Active Comparator
Arm Description
Have not previously received SD NVP; assigned to receive either an NNRTI- or PI-based regimen as a part of the study IMPAACT P1060
Intervention Type
Drug
Intervention Name(s)
Lamivudine
Other Intervention Name(s)
3TC
Intervention Description
Taken orally twice daily
Intervention Type
Drug
Intervention Name(s)
Lopinavir/Ritonavir
Other Intervention Name(s)
LPV/r
Intervention Description
Taken orally twice daily
Intervention Type
Drug
Intervention Name(s)
Nevirapine
Other Intervention Name(s)
NVP
Intervention Description
Taken orally twice daily
Intervention Type
Drug
Intervention Name(s)
Zidovudine
Other Intervention Name(s)
ZDV
Intervention Description
Taken orally twice daily
Primary Outcome Measure Information:
Title
Parasitemia in blood samples
Time Frame
Throughout study
Secondary Outcome Measure Information:
Title
Time of initiation of treatment for clinical malaria requiring conventional anti-malarial therapy
Time Frame
Throughout study
Title
Severity of malarial disease
Time Frame
Throughout study
Title
Measured anti-malaria IgG, protein in plasma, and mRNA transcripts in PBMC of chemokines
Time Frame
Throughout study
Title
IL4-589C/T genotypes
Time Frame
Throughout study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
35 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Enrolling in study IMPAACT P1060
Parent/legal guardian agrees to seek medical care for intercurrent illness at the study site, whenever possible, and agree to not use at-home remedies for febrile illness in the child
Exclusion Criteria:
None.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charlotte Hobbs, MD
Organizational Affiliation
NYU Langone Health
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
William Borkowsky, MD
Organizational Affiliation
NYU Langone Health
Official's Role
Study Chair
Facility Information:
Facility Name
University of North Carolina Lilongwe (12001)
City
Lilongwe
Country
Malawi
Facility Name
Makerere University - JHU Research Collaboration (30293)
City
Kampala
Country
Uganda
Facility Name
George Clinic CRS (30273)
City
Lusaka
Country
Zambia
12. IPD Sharing Statement
Citations:
PubMed Identifier
18575485
Citation
Adetifa IM, Akinsulie AO, Temiye EO, Iroha EO, Ezeaka VC, Mafe AG, Grange AO. Effect of antiretroviral therapy on asymptomatic malaria parasitaemia in HIV-1 infected children. Niger Postgrad Med J. 2008 Jun;15(2):120-5.
Results Reference
background
PubMed Identifier
18332766
Citation
Brahmbhatt H, Sullivan D, Kigozi G, Askin F, Wabwire-Mangenm F, Serwadda D, Sewankambo N, Wawer M, Gray R. Association of HIV and malaria with mother-to-child transmission, birth outcomes, and child mortality. J Acquir Immune Defic Syndr. 2008 Apr 1;47(4):472-6. doi: 10.1097/QAI.0b013e318162afe0.
Results Reference
background
PubMed Identifier
27936233
Citation
Hobbs CV, Gabriel EE, Kamthunzi P, Tegha G, Tauzie J, Petzold E, Barlow-Mosha L, Chi BH, Li Y, Ilmet T, Kirmse B, Neal J, Parikh S, Deygoo N, Jean Philippe P, Mofenson L, Prescott W, Chen J, Musoke P, Palumbo P, Duffy PE, Borkowsky W; P1068s Study Team. Malaria in HIV-Infected Children Receiving HIV Protease-Inhibitor- Compared with Non-Nucleoside Reverse Transcriptase Inhibitor-Based Antiretroviral Therapy, IMPAACT P1068s, Substudy to P1060. PLoS One. 2016 Dec 9;11(12):e0165140. doi: 10.1371/journal.pone.0165140. eCollection 2016.
Results Reference
derived
Learn more about this trial
Differences in Malaria Infection Levels in HIV-infected Infants and Children Receiving PI- and NNRTI-based HAART
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