The purpose of this study was to evaluate the safety, efficacy, and pharmacokinetic of the combination M5717 plus pyronaridine in participants with acute uncomplicated Plasmodium falciparum malaria.
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Cohort A: Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious TEAEs and Related TEAEs
Timeframe: Day 1 up to Day 43
Cohort A: Number of Participants With Clinically Significant Change From Baseline in Safety Laboratory Parameters
Timeframe: Day 1 up to Day 29
Cohort A: Number of Participants With Clinically Significant Change From Baseline in 12-lead Electrocardiogram (ECG) Findings
Timeframe: Day 1 up to Day 29
Cohort A: Number of Participants With Clinically Significant Change From Baseline in Vital Signs
Timeframe: Day 1 up to Day 29
Cohort B0: Percentage of Participants With Polymerase Chain Reaction (PCR)-Adjusted Adequate Clinical and Parasitological Response (ACPR)
Timeframe: At Day 29