Efficacy and Safety of Ixekizumab in Patients with Refractory Guttate Psoriasis

PHASE2/PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

May 31, 2025

Primary Completion Date

June 30, 2025

Study Completion Date

June 30, 2026

Conditions
Guttate Psoriasis
Interventions
BIOLOGICAL

Ixekizumab

Participants will receive an initial dose of 160 mg (two injections of 80 mg) ixekizumab subcutaneously at week 0, followed by 80 mg at weeks 2, 4, 6, 8, 10, and 12.

All Listed Sponsors
lead

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

NCT06374979 - Efficacy and Safety of Ixekizumab in Patients with Refractory Guttate Psoriasis | Biotech Hunter | Biotech Hunter