drugset / Trial / NCT05442788

A Study of HB0017 in Patients With Moderate to Severe Plaque Psoriasis

NCT05442788 ↗

Phase 1 Completed 30 enrolled Huabo Biopharm Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, dose-escalation Phase Ib study to evaluate the safety, tolerability, and pharmacokinetics of HB0017 following multiple dose in patients with moderate to severe plaque psoriasis.

Timeline

Start
2021-09-02
Primary completion
2022-05-31
Completion
2022-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject HB0017 Monoclonal antibody 150 mg Subcutaneous
Subject HB0017 Monoclonal antibody 300 mg Subcutaneous
Subject HB0017 Monoclonal antibody 450 mg Subcutaneous

Indications