drugset / Trial / NCT06231381

Efficacy and Safety of HB0034 in Patients with Generalized Pustular Psoriasis (GPP)

NCT06231381 ↗

Phase 2 Recruiting 33 enrolled Shanghai Huaota Biopharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase II, multicenter, double-blind, randomized, placebo parallel-controlled clinical trial to evaluate the efficacy and safety of HB0034 in patients with generalized pustular psoriasis (GPP) presenting with an acute flare of moderate to severe intensity.

Timeline

Start
2024-02-29
Primary completion
2025-02-13
Completion
2025-11-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator HB0034 Monoclonal antibody — Intravenous