To Compare the Pharmacokinetics, Safety and Immunogenicity of CT-P55 and Cosentyx in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

172

Participants

Timeline

Start Date

January 12, 2024

Primary Completion Date

August 29, 2024

Study Completion Date

September 6, 2024

Conditions
Healthy Male Subjects
Interventions
BIOLOGICAL

CT-P55

150 mg in 1.0 mL, administered as a single SC injection via PFS

BIOLOGICAL

US-licensed Cosentyx

150 mg in 1.0 mL, administered as a single SC injection via PFS

BIOLOGICAL

EU-approved Cosentyx

150 mg in 1.0 mL, administered as a single SC injection via PFS

Trial Locations (4)

232-0064

Yokohama Minoru Clinic, Yokohama

Unknown

SOUSEIKAI Nishikumamoto Hospital, Kumamoto

532-0003

Medical Corporation Heishinkai OPHAC Hospital, Osaka

108-8642

Kitasato University Kitasato Institute Hospital, Minato-ku

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celltrion

INDUSTRY