Single Ascending Oral Dose Phase 1 Study of ID110521156 in Healthy Adult Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

November 20, 2023

Primary Completion Date

July 11, 2024

Study Completion Date

July 11, 2024

Conditions
Healthy Adult Subjects
Interventions
DRUG

ID110521156

subjects will receive a single oral dose of IMP. In the morning (all procedures must be performed at the similar clock time) on Day 1

DRUG

Placebo of ID110521156

subjects will receive a single oral dose of IMP. In the morning (all procedures must be performed at the similar clock time) on Day 1

Trial Locations (1)

03080

Seoul National University Hospital, Seoul

Sponsors
All Listed Sponsors
collaborator

YUNOVIA CO.,LTD.

UNKNOWN

lead

IlDong Pharmaceutical Co Ltd

INDUSTRY

NCT06063291 - Single Ascending Oral Dose Phase 1 Study of ID110521156 in Healthy Adult Subjects | Biotech Hunter | Biotech Hunter