Malaria Clinical Trial
Official title:
Studies of P. Vivax and P. Falciparum Malaria in Cambodia
This study, conducted by the National Center for Parasitology, Entomology and Malaria Control
of Cambodia s Ministry of Health and the National Institute of Allergy and Infectious
Diseases, will explore whether the following factors confer protection against malaria and
associated anemia: certain blood groups, the hemoglobin E variant, G6PD-deficiency and
alpha-thalassemia. Malaria is caused by parasites (P. falciparum and P. vivax) that are
transmitted to humans through mosquito bites. This protocol includes two studies, a cohort
study and a P. vivax collection study.
Individuals are eligible for enrollment in the studies as follows:
Cohort study:
Residents of all ages of Kandal, Ekapheap and Sangkumthmey villages (Thmar Da commune) who
plan to remain in Thmar Da commune for the next 5 years.
P. vivax collection study:
2 years of age and older
Participating in NIAID protocol 05-I- N210 ( Severe Malaria and Anti-malarial Drug Resistance
in Cambodia ) and diagnosed with P. vivax malaria
Participants undergo the following procedures:
Cohort study:
Baseline evaluation, including the following:
- Collection of demographic information
- Malaria history, temperature measurement and review of current symptoms, if any
- Blood draw of 300 microliters
- Additional blood draw of 10 milliliters in selected adults 18 years of age and older
Treatment with artesunate-piperaquine at a commune health post for subjects who develop
malaria
Contact once a year for 5 years to determine continued residency in Thmar Da commune
P. vivax collection study:
- Medical history and physical examination
- Hemoglobin level measurement
- Blood draw
- Treatment with chloroquine
- Blood draw 3 to 5 weeks after treatment in some patients 18 years of age or older
Cohort study. Hemoglobin (Hb) and red blood cell (RBC) polymorphisms that give rise to HbE,
alpha-thalassemia, G6PD-deficiency, and ABO blood groups occur at high frequency along the
Thailand-Cambodia border, where Plasmodium vivax and P. falciparum have been and continue to
be transmitted. To determine whether these Hb/RBC polymorphisms have been naturally selected
because they confer protection against malaria and malaria-associated anemia, we will conduct
a cohort study of ethnic Khmer in Cambodia. Approximately 1000 individuals of all ages will
be genotyped for the four polymorphisms listed above and then followed for 5 years to
determine the mean incidence rates for both P. vivax and P. falciparum malaria, stratified by
genotype. Incidence rate ratios (IRRs) will be calculated for each polymorphism relative to
the wildtype genotype. Differences between Hb levels during acute episodes of malaria and Hb
levels at baseline will also be calculated to determine if Hb/RBC polymorphisms influence the
degree of malaria-associated anemia.
P. vivax collection study. Unlike P. falciparum, P. vivax cannot be efficiently cultivated in
vitro. Improved cultivation methods are needed to make progress on nearly all aspects of P.
vivax malariology, including pathogenesis, naturally-acquired immunity, vaccination, and
antimalarial drug resistance. We plan to improve both short- and long-term cultivation
methods in order to test various hypotheses of P. vivax pathogenesis and protection. Using
freshly obtained parasite isolates from individuals with P. vivax malaria, we will test
whether Hb/RBC polymorphisms influence potentially pathogenic properties of P. vivax
parasites, such as their ability to bind non-infected RBCs and other host cells. It is
believed that P. vivax selectively invades reticutocytes. This tropism has frustrated
attempts at long-term cultivation of this parasite, which requires a constant source of
reticulocyte-rich blood not easily obtained even in developed countries. The host
reticulocyte receptor that mediates the highly selective tropism of P. vivax has not been
identified. Fresh P. vivax parasites will also be used in in vitro experiments to identify
the putative receptor that defines reticulocyte tropism. Any P. vivax ligand that bound
selectively to a reticulocyte receptor will then be discovered and worked up as a promising
vaccine candidate.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04601714 -
Baseline Cohort Malaria Morbidity Study
|
||
| Withdrawn |
NCT04020653 -
A Study to Assess the Safety and Efficacy of 5-aminolevulinic Acid Hydrochloride (5-ALA HCl) and Sodium Ferrous Citrate (SFC) Added on Artemisinin-based Combination Therapy (ACT) in Adult Patients With Uncomplicated Malaria
|
Phase 2 | |
| Terminated |
NCT04368910 -
Safety and Efficacy of Pyronaridine Artesunate Vs Chloroquine in Children and Adult Patients With Acute Vivax Malaria
|
Phase 3 | |
| Completed |
NCT03641339 -
Defining Skin Immunity of a Bite of Key Insect Vectors in Humans
|
N/A | |
| Completed |
NCT02544048 -
Markers of T Cell Suppression: Antimalarial Treatment and Vaccine Responses in Healthy Malian Adults
|
||
| Completed |
NCT00527163 -
Role of Nitric Oxide in Malaria
|
||
| Not yet recruiting |
NCT05934318 -
L-ArGinine to pRevent advErse prEgnancy Outcomes (AGREE)
|
N/A | |
| Active, not recruiting |
NCT04704674 -
Community Dynamics of Malaria Transmission in Humans and Mosquitoes in Fleh-la and Marshansue, Salala District, Bong County, Liberia
|
||
| Completed |
NCT03276962 -
Efficacy, Safety and Immunogenicity Study of GSK Biologicals' Candidate Malaria Vaccine (SB257049) Evaluating Schedules With or Without Fractional Doses, Early Dose 4 and Yearly Doses, in Children 5-17 Months of Age
|
Phase 2 | |
| Completed |
NCT04966871 -
Safety, Tolerability and Efficacy of PfSPZ Vaccine Against Heterologous CHMI in US Malaria naïve Adults
|
Phase 1 | |
| Completed |
NCT00289185 -
Study of Safety, Immunogenicity and Efficacy of a Candidate Malaria Vaccine in Tanzanian Infants
|
Phase 2 | |
| Recruiting |
NCT03937817 -
Collection of Human Biospecimens for Basic and Clinical Research Into Globin Variants
|
||
| Active, not recruiting |
NCT06153862 -
Africa Ready Malaria Screening
|
N/A | |
| Completed |
NCT04545905 -
Antenatal Care as a Platform for Malaria Surveillance: Utilizing Community Prevalence Measures From the New Nets Project to Validate ANC Surveillance of Malaria in Burkina Faso
|
||
| Recruiting |
NCT06278181 -
Diabetes, Metabolic Syndrome and Risk of Malaria in Cameroon
|
||
| Completed |
NCT02909712 -
Cardiac Safety of Dihydroartemisinin-Piperaquine Amongst Pregnant Women in Tanzania
|
Phase 2 | |
| Withdrawn |
NCT02793414 -
Diagnostic Utility of Volatile Organic Compounds in Human Breath for Acute Clinical Malaria in Ethiopia
|
||
| Completed |
NCT02793622 -
Prevention of Malaria in HIV-uninfected Pregnant Women and Infants
|
Phase 3 | |
| Withdrawn |
NCT02793388 -
A Trial on Supervised Primaquine Use in Ethiopia
|
Phase 4 | |
| Completed |
NCT02536222 -
Accelerating the Reduction of Malaria Transmission in Kanel, Ranérou and Linguère Districts
|
Phase 4 |