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COMPLETED
NCT04675931
PHASE2

To Evaluate Efficacy, Safety, Tolerability and PK of Intravenous Cipargamin in Participants With Severe Plasmodium Falciparum Malaria

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

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

DRUG

Cipargamin

Cipargamin, 20 mg or 40 mg, by intravenous administration of solution for injection

DRUG

IV Artesunate

Artesunate, 2.4 mg/kg or 3 mg/kg, by intravenous administration of reconstituted solution

DRUG

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