Malaria, Falciparum, HIV Infections
Conditions
Keywords
uncomplicated malaria, HIV/AIDS, drug interactions, antimalarial drug efficacy, antiretrovirals, pharmacovigilance, Tanzania
Brief summary
As HIV/AIDS is spreading in malaria-endemic countries, many patients here will need concomitant treatment for both infections. Effective combination treatments are available for both malaria (artemisinin-based combination treatments, ACTs) and HIV/AIDS (antiretroviral combination treatments, ARTs), and these treatments are presently recommended for concomitant use by ministries of health in many endemic countries, including Tanzania. However, theoretically some of these drugs may be involved in harmful interactions with each other, as they share common cytochrome enzymes involved in their metabolism. Such interactions could lead to less effective treatments and/or adverse effects, as a consequence of reduced or increased drug levels, respectively. Only little clinical and pharmacological information is however yet available to guide clinicians and policy-makers on this issue. The main aim of the InterACT study in Tanzania is to conduct a series of detailed observational studies of clinical and paraclinical safety, therapeutic efficacy and pharmacokinetic interactions between the currently nationally recommended first-line treatment for malaria, artemether-lumefantrine, and first-line antiretroviral treatments, primarily nevirapine-based combinations, for HIV/AIDS. The studies will be conducted among patients with uncomplicated malaria, who attend the HIV/AIDS Care and Treatment Clinic and Muheza Designated District Hospital in Muheza, north-eastern Tanzania, which is an area characterized by intense transmission of Plasmodium falciparum malaria and with a prevalence of HIV around 8-10%. The study is expected to inform guidelines for the treatment of malaria in patients with HIV/AIDS in Tanzania, and elsewhere.
Interventions
Standard treatment-dose of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria according to national treatment guidelines
Sponsors
National Institute for Medical Research, Tanzania
London School of Hygiene and Tropical Medicine
University of Copenhagen
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
15 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
* HIV-positive and HIV-negative patients with confirmed P. falciparum infection in the presence of either measured fever (\> 37.5°C) or a history of fever within the previous 24 hours; for HIV-positive patients also afebrile patients are eligible in the presence of other symptoms of malaria (e.g., coughing, diarrhea, headache, nausea, body weakness, body pain). * Not being pregnant or lactating. * Absence of history of clinically significant hypersensitivity reactions to any of the study medicines being evaluated. * For HIV-positive patients on cART, successful adherence to treatment without prominent adverse events for a period of a minimum of six weeks prior to the date of enrollment will be required. * Easy access to the health facility (travel time \< 1 hour) and the ability to attend the stipulated follow-up visits. * Informed consent provided by the patient or by a parent/guardian
Exclusion criteria
* Patients below body weight of 10 kilograms (for under fives). * Existence of underlying chronic severe illness (e.g., cardiac, renal or hepatic disease). * No use within the previous four weeks prior to enrollment of any other antimalarial or other drug with antimalarial activity (with the exception of drugs required as part of standard treatment of HIV/AIDS, e.g., sulfamethoxazole and trimethoprim).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical and parasitological efficacy of artemether-lumefantrine; incidence and severity of treatment-related clinical and paraclinical adverse events; changes in pharmacokinetic profiles of artemether-lumefantrine. | 42 days of post-treatment follow-up |
Secondary
| Measure | Time frame |
|---|---|
| Changes in pharmacokinetic profiles of nevirapine-based and other used antiretrovirals; | 42 days of post-treatment follow-up |
Countries
Tanzania
Outcome results
None listed