Safety, Tolerability, and Pharmacokinetics of ID119031166M With the Exploration of Pharmacodynamic Effects

PHASE1TerminatedINTERVENTIONAL
Enrollment

67

Participants

Timeline

Start Date

October 10, 2022

Primary Completion Date

April 12, 2024

Study Completion Date

April 12, 2024

Conditions
Healthy Participants
Interventions
DRUG

ID119031166M

The participants will receive a single oral dose of ID119031166M or once daily oral doses of ID119031166M for 14 days.

DRUG

Placebo

The participant will receive a oral dose of Placebo.

Trial Locations (1)

91206

California Clinical trials medical group/PAREXEL, Glendale

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

collaborator

YUNOVIA CO.,LTD.

UNKNOWN

lead

IlDong Pharmaceutical Co Ltd

INDUSTRY