Biologic Therapy for Generalized Pustular Psoriasis

CompletedOBSERVATIONAL
Enrollment

65

Participants

Timeline

Start Date

July 1, 2019

Primary Completion Date

December 30, 2022

Study Completion Date

December 30, 2023

Conditions
Generalized Pustular Psoriasis
Interventions
DRUG

After exclusion of relevant contraindications, participants received subcutaneous ustekinumab/secukinumab therapy.

During the treatment period, participants received either ustekinumab at weeks 0, 4, 16, and every 12 weeks thereafter until week 48, or secukinumab at weeks 0, 1, 2, 3, and 4, and every 4 weeks thereafter until week 48. The dose of ustekinumab/secukinumab was referenced to the dose used for moderate to severe plaque psoriasis. The single dose of ustekinumab was 45 mg for adult subjects weighing ≤ 100 kg, and 90 mg for subjects weighing \> 100 kg. The ustekinumab dosage for pediatric participants was 0.75 mg/kg for participants weighing \< 60 kg; 45 mg for pediatric participants weighing 60 kg to 100 kg; and 90 mg for pediatric participants weighing \> 100 kg. The secukinumab dosage was 300mg for adult humans. Pediatric participants received a dose based on their weight category ( \<50 kg, ≥50 kg): participants weighing \< 50 kg received 75 mg, those weighing ≥ 50 kg received 150 mg.

Trial Locations (1)

350000

First Affiliated Hospital of Fujian Medical University, Fuzhou

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Chao Ji

OTHER