Single Ascending Dose Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HM15912(Sonefpeglutide) in Healthy Korean Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

October 8, 2019

Primary Completion Date

November 10, 2020

Study Completion Date

May 3, 2021

Conditions
Pharmacology
Interventions
DRUG

HM15912

The study will be conducted in approximately 5 sequential dosing cohorts, enrolling 8 subjects per cohort. Subjects will be randomized to HM15912 or placebo in a ratio of 6:2 (6 active, 2 placebo).

DRUG

Placebo

The study will be conducted in approximately 5 sequential dosing cohorts, enrolling 8 subjects per cohort. Subjects will be randomized to HM15912 or placebo in a ratio of 6:2 (6 active, 2 placebo).

Trial Locations (1)

05505

Asan Medical Center, Seoul

All Listed Sponsors
lead

Hanmi Pharmaceutical Company Limited

INDUSTRY

NCT04076293 - Single Ascending Dose Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HM15912(Sonefpeglutide) in Healthy Korean Subjects | Biotech Hunter | Biotech Hunter