Safety and Efficacy of Imatinib in Combination With Artemether-Lumefantrine for Uncomplicated Malaria

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age1-55
SponsorVictoria Biomedical Research Institute

About this trial

This study is investigating an innovative approach to treating uncomplicated malaria by adding a drug called Imatinib to the current standard of care, Artemether + Lumefantrine (AL). The researchers hope this combination, known as ALIM, will clear infections faster and stop the spread of drug-resistant parasites that are becoming a major threat in Africa

Eligibility criteria

Qualifiers

Patients diagnosed with symptomatic mild to moderate P. falciparum malaria with a parasite density of >= 5000 parasites/μl

Adult male, age 18-55 years old or adult female, age 18-55 years that are post-menopausal, or test negative on a pregnancy test and will be on active birth control through to the end of the follow up period.

Provision of informed consent and agrees to hospital admission for 48-72hrs

Good health condition other than malaria

Disqualifiers

Prospective study participant, LAR and/or impartial witness (where applicable) declines to provide informed consent.

significant confusion or impaired consciousness (including unarousable coma)

multiple convulsions (more than two episodes within 24 hours),

respiratory distress

Trial design

Treatments tested in this trial

  • Artemether lumefantrine tablets
  • Artemether Lumefantrine and Imatinib Mesylate

Treatment groups

1,116 Participants
are divided into 5 treatment groups

Sponsors and collaborators