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To Evaluate Efficacy, Safety, Tolerability and PK of Intravenous Cipargamin in Participants With Severe Plasmodium Falciparum Malaria
Sponsor: Novartis Pharmaceuticals
Summary
The purpose of this study was to identify the safe and effective dose of intravenous cipargamin in participants with moderately severe and severe malaria. The study also intended to evaluate clinical treatment success using a novel clinical endpoint for drug development in severe malaria. Severe malaria is a medical emergency and is affecting primarily young children in Africa. Injectable artesunate is the standard of care for the treatment of severe malaria and is highly efficacious. However, the spread of artemisinin-resistance in Plasmodium falciparum in Asian countries poses a threat for future treatment of patients with this life-threatening disease. To mitigate this risk, there is a need for another drug in malaria-endemic countries. Cipargamin treatment results in rapid clearance of parasites, including artemisinin-resistant parasites.
Official title: An Adaptive, Randomized, Active-controlled, Open-label, Sequential Cohort, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of Intravenous Cipargamin (KAE609) in Adult and Pediatric Participants With Severe Plasmodium Falciparum Malaria (KARISMA - KAE609's Role In Severe Malaria)
Key Details
Gender
All
Age Range
6 Months - 100 Years
Study Type
INTERVENTIONAL
Enrollment
254
Start Date
2022-03-07
Completion Date
2025-08-20
Last Updated
2026-04-09
Healthy Volunteers
No
Conditions
Interventions
Cipargamin
Cipargamin, 20 mg or 40 mg, by intravenous administration of solution for injection
IV Artesunate
Artesunate, 2.4 mg/kg or 3 mg/kg, by intravenous administration of reconstituted solution
Coartem
Oral standard of care (Coartem tablets, dosed per weight, as per label)
Locations (9)
Novartis Investigative Site
Burkina Faso, Burkina Faso
Novartis Investigative Site
Ouagadougou, Burkina Faso
Novartis Investigative Site
Abidjan, Côte d’Ivoire
Novartis Investigative Site
Agboville, Côte d’Ivoire
Novartis Investigative Site
Kinsasha, Democratic Republic of Congo, Democratic Republic of the Congo
Novartis Investigative Site
Siaya, Kenya
Novartis Investigative Site
Manhiça, Maputo Province, Mozambique
Novartis Investigative Site
Kigali, Rwanda
Novartis Investigative Site
Tororo, Uganda