First-in-Human Study to Assess the Safety, Tolerability and Pharmacokinetics of MMV367

PHASE1CompletedINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

July 29, 2022

Primary Completion Date

January 25, 2023

Study Completion Date

January 25, 2023

Conditions
Malaria,Falciparum
Interventions
DRUG

MMV367

Single dose dispersed in sterile water, fasted.

DRUG

Placebo

Single Dose dispersed in sterile water, fasted.

DRUG

MMV367 (Fed 440mg)

Single dose dispersed in sterile water with a high fat meal.

DRUG

MMV367

Single dose dispersed in sterile water, fasted, administered for 3 consecutive days.

DRUG

Placebo

Single dose dispersed in sterile water, fasted, administered for 3 consecutive days.

DRUG

MMV367 (Fasted 440mg)

Single dose dispersed in sterile water fasted.

Trial Locations (1)

NG11 6JS

Quotient Sciences, Nottingham

Sponsors
All Listed Sponsors
collaborator

Quotient Sciences

INDUSTRY

collaborator

Swiss BioQuant

INDUSTRY

collaborator

Banook Group

INDUSTRY

collaborator

The Doctors Laboratory Ltd

INDUSTRY

collaborator

GlaxoSmithKline

INDUSTRY

lead

Medicines for Malaria Venture

OTHER

NCT05507970 - First-in-Human Study to Assess the Safety, Tolerability and Pharmacokinetics of MMV367 | Biotech Hunter | Biotech Hunter