Safety, Tolerability, and Pharmacokinetic Evaluations of CKR-051 After Transdermal Administration in Healthy Male Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

April 25, 2023

Primary Completion Date

January 8, 2024

Study Completion Date

January 8, 2024

Conditions
Healthy
Interventions
DRUG

CKR-051 Dose 1

Subjects will be administered 5 g of CKR-051.

DRUG

CKR-051 Dose 2

Subjects will be administered 10 g of CKR-051.

DRUG

CKR-051 Dose 3

Subjects will be administered 10 g of CKR-051.

DRUG

CKR-051 Dose 4

Subjects will be administered 10 g of CKR-051.

DRUG

Placebo

Placebo comparator.

Trial Locations (1)

03080

Seoul National University Hospital, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CK Regeon Inc.

INDUSTRY