Study on the Treatment of Vivax Malaria (VHX)

University of Oxford

Status and phase: Completed; Phase 3

Conditions: Vivax Malaria

Treatments: Drug: Chloroquine; Drug: Chloroquine/Primaquine; Drug: Artesunate

Study type: Interventional

Funder types: Other

Identifiers

NCT01074905

SMRU0908

Details and patient eligibility

About

This is a randomised open label trial with follow up for 1 year. 660 adults and children above 6 months diagnosed with acute Plasmodium vivax will be randomised into 3 groups, either chloroquine, artesunate, or chloroquine/primaquine therapy. Participants will be screened on the day of inclusion then followed weekly for 8 visits and every 4 weeks until week 52. The primary objective of the study is to compare the efficacy of the WHO and Thai Ministry of Public Health recommended radical curative regimen of chloroquine and primaquine with the currently used monotherapy regimens of chloroquine and artesunate along the Thai-Burmese border.

Full description

Considerably less attention has been paid to Plasmodium vivax epidemiology than Plasmodium falciparum. In areas of relatively low unstable transmission, which comprise the majority of P.vivax affected areas, vivax malaria is predominantly a disease of children (Luxemburger et al 1999). Chloroquine has long been the standard treatment for vivax malaria. Primaquine is recommended for radical cure of vivax malaria, but is difficult to administer due to dosing duration and side effects.

This study aims to characterize the epidemiologic history comparing the efficacy of 3 antimalarial regimens (chloroquine, artesunate, and chloroquine/primaquine) for plasmodium vivax in western Thailand. Chloroquine is currently the standard of treatment for Plasmodium vivax. Due to the long half-life or chloroquine, the first relapse of vivax malaria may be delayed. In contrast, artesunate has a very short half-life, thus, having no impact on first relapse. It is not known whether chloroquine reduces the overall number of relapses, or only delays the first relapse. There are many important questions about the biology of vivax malaria of relevance to treatment that remain unanswered. For example is the number of relapses per infection (i.e. per successful inoculation) predetermined or adaptive? If it is predetermined then suppression of the first relapse (as with chloroquine, mefloquine or piperaquine) will reduce the total number of relapses and this is a clear benefit. If it is adaptive then these drugs will simply delay the relapses and there is less clear benefit. These various uncertainties illustrate the importance of detailed comparative longitudinal evaluations. In order to characterize the biology of vivax malaria, it will be necessary to compare regimens with and without primaquine. Because of the challenges that face primaquine prescription (side effects, toxicity in G6PD deficient patients and duration of treatment), it is not commonly deployed along the Thai Burma border. In effect, we will be comparing usual practice (non primaquine regimens) with the recommended WHO and Thai MOPH practice (use of primaquine for 14 days). The information we will gather is crucial to the understanding of chloroquine and its effect on the vivax parasite. This will lead to future studies and invariably change the way we treat vivax malaria.

Enrollment: 655 patients

Sex: All

Ages: 6+ months old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Adults and children > 6 months
• Weight > 7 kg for children
• Have not had primaquine since last Pv episode
• Participant (or parent/guardian if < 18 years old) is willing and able to give written informed consent
• Microscopic diagnosis of Plasmodium vivax mono-infection
• Ability (in the investigators opinion) and willingness of patient or parent/guardian to comply with all study requirements

Exclusion Criteria

• Allergy to artesunate, chloroquine or primaquine
• Severe malaria
• Patients with microscopic diagnosis of co-infection with Plasmodium falciparum
• Presence of any condition which in the judgement of the investigator would place the subject at undue risk or interfere with the results of the study
• Inability to tolerate oral medication
• Pregnancy
• Blood transfusion in the last 3 months
• Antimalarial in last 2 months

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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655 participants in 3 patient groups

Artesunate

Active Comparator group

Description:

2 mg/kg/day as single daily dose given for 5 days; maximum dose range is 1.6 to 2.4 mg/kg/day or a total of 8 to 12 mg/kg.

Treatment:

Drug: Artesunate

Chloroquine

Active Comparator group

Description:

25 mg base/kg given in divided doses (10,10,5) over 3 days; Absolute range 20-30 mg/kg.

Treatment:

Drug: Chloroquine

Chloroquine/Primaquine

Experimental group

Description:

Chloroquine 3 days and Primaquine 14 days

Treatment:

Drug: Chloroquine/Primaquine