Comparative Study of CMAB015 and Secukinumab for Patients With Moderate to Severe Plaque Psoriasis

PHASE3Active, not recruitingINTERVENTIONAL
Enrollment

336

Participants

Timeline

Start Date

August 27, 2024

Primary Completion Date

June 30, 2025

Study Completion Date

March 31, 2026

Conditions
Psoriasis
Interventions
BIOLOGICAL

CMAB015

Patients would receive 300 mg CMAB007 subcutaneous injections at week 0, 1, 2, 3, 4, 8 as induction therapy. Patients who obtain a 75% improvement relative to baseline in PASI scores would receive 300 mg CMAB007 subcutaneous injections every 4 weeks as maintain therapy, until the last treatment at week 48.

BIOLOGICAL

Secukinumab

Patients would receive 300 mg secukinumab subcutaneous injections at week 0, 1, 2, 3, 4, 8 as induction therapy. Patients who obtain a 75% improvement relative to baseline in PASI scores would receive 300 mg secukinumab subcutaneous injections every 4 weeks as maintain therapy, until the last treatment at week 48.

Trial Locations (1)

Unknown

Huashan Hospital, Shanghai

All Listed Sponsors
lead

Taizhou Mabtech Pharmaceutical Co.,Ltd

INDUSTRY

NCT06398652 - Comparative Study of CMAB015 and Secukinumab for Patients With Moderate to Severe Plaque Psoriasis | Biotech Hunter | Biotech Hunter