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Differences in Malaria Infection Levels in HIV-infected Infants and Children Receiving PI- and NNRTI-based HAART

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

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00719602
Enrollment
105
Registered
2008-07-21
Start date
2009-08-31
Completion date
2013-08-31
Last updated
2016-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections, Malaria

Keywords

Coinfection

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.

Interventions

DRUGLamivudine

Taken orally twice daily

DRUGLopinavir/Ritonavir

Taken orally twice daily

DRUGNevirapine

Taken orally twice daily

DRUGZidovudine

Taken orally twice daily

Sponsors

National Institute of Allergy and Infectious Diseases (NIAID)
CollaboratorNIH
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
6 Months to 35 Months
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Parasitemia in blood samplesThroughout study

Secondary

MeasureTime frame
Time of initiation of treatment for clinical malaria requiring conventional anti-malarial therapyThroughout study
Severity of malarial diseaseThroughout study
Measured anti-malaria IgG, protein in plasma, and mRNA transcripts in PBMC of chemokinesThroughout study
IL4-589C/T genotypesThroughout study

Countries

Malawi, Uganda, Zambia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026