Southeast Asia Dose Optimization of Tafenoquine

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age2+
SponsorUniversity of Oxford

About this trial

Tafenoquine was recently approved by regulatory authorities in the USA and Australia. Tafenoquine is an alternative radical curative treatment to primaquine acting against the dormant liver stage of Plasmodium vivax (the hypnozoite). Tafenoquine (an 8-aminoquinoline) has the substantial advantage of single dosing as compared to a 14-day course of primaquine to achieve radical cure. The recommended tafenoquine dose is 300 mg, which was shown to be significantly worse in radical curative efficacy to a total primaquine dose of 3.5 mg/kg in Southeast Asia. The cure rate of tafenoquine 300 mg in Southeast Asian study sites was only 74%. The comparator 3.5 mg/kg total primaquine dose is the standard and most commonly used dose globally, but in Southeast Asia and the Western Pacific, higher doses of primaquine are needed for radical cure. This study aims to determine the optimal dose of tafenoquine in Southeast Asia.

Addendum for Indonesia: The INSPECTOR trial results showed that tafenoquine 300mg was not efficacious for radical cure (79% probability for recurrence after treatment). The comparator arm, low-dose primaquine 3.5mg/kg divided equally over 14 days, showed a 48% probability of recurrence after treatment). The standard of care for radical cure in Indonesia is high-dose primaquine 7mg/kg divided in 7 daily doses).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with symptomatic P. vivax mono-infection as diagnosed by microscopy

Fever or history of fever in the previous 7 days

Quantitative G6PD activity ≥70% of the population median

Weight >10 kg and ≥2 years old

Disqualifiers

Pregnancy

Lactation

Hb < 8 g/dL

Severe malaria

Trial design

Design model

Parallel

Treatments tested in this trial

  • Tafenoquine

    Drug

    Tafenoquine will be given as 100mg coated tablets. Tablets will be given based on weight bands.

  • Chloroquine

    Drug

    Chloroquine will be given as daily dose over 3 days (25mg/kg total dose divided 10/10/5mg/kg)

  • Artemether 20 mg-Lumefantrine 120 mg

    Drug

    Artemether-lumefantrine will be given twice daily over 3 days. Whole tablets will be given based on weight bands.

  • Primaquine

    Drug

    Primaquine will be given once daily over 7 days (7mg/kg total dose divided 1mg/kg/day) as per the national malaria guidelines.

  • Dihydroartemisinin 40 mg-Piperaquine 320 mg

    Drug

    Dihydroartemisinin-piperaquine will be given once daily over 3 days. Whole tablets will be given based on weight bands.

Treatment groups

820 Participants
are divided into 3 treatment groups
Group A: Tafenoquine standard dose (TQ-current)Active comparator 3 interventions
Group B: Tafenoquine 50% higher dose (TQ-higher)Active comparator 3 interventions
Group C: Primaquine standard high-dose (PQ)Active comparator 2 interventions

Trial outcomes

Primary outcomes

1

Microscopy positive P. vivax recurrence after radical treatment up to month 4

Time frame
At month 4

Secondary outcomes

1

Sub-microscopic P. vivax recurrence after radical treatment between day 28 and month 4

Time frame
At Day 28; Month 4
2

Sub-microscopic P. vivax recurrence with very low parasite density after radical cure treatment at days 14 and 21

Time frame
At Day 14 and 21
3

Number of serious adverse events (e.g., hospitalization for symptomatic hemolysis or methemoglobinemia)

Time frame
At Days 1, 2, 7, 14 and Months 1, 2, 3, 4
4

Number of adverse events (e.g., gastrointestinal symptoms)

Time frame
At Days 1, 2, 7, 14 and Months 1, 2, 3, 4

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.