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Trials / Recruiting

RecruitingNCT06477237

Study of Efficacy and Safety of HB0017 in Patients With Moderate to Severe Plaque Psoriasis

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of HB0017 Injection in Patients With Moderate to Severe Plaque Psoriasis

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
Huabo Biopharm Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a multicenter, randomized, double-blind, placebo-controlled, phase III clinical study which is designed to determine the efficacy, safety, immunogenicity and pharmacokinetics, and pharmacodynamics of HB0017 Injection in the treatment of moderate to severe plaque psoriasis in adults.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHB0017 Q4WHB0017 at W0,1,2,4,8+HB0017Q4W
BIOLOGICALHB0017 Q8WHB0017 at W0,1,2,4,8+HB0017Q8W
BIOLOGICALplaceboplacebo at W0,1,2,4,8+HB0017Q4W

Timeline

Start date
2024-03-01
Primary completion
2024-08-01
Completion
2025-12-01
First posted
2024-06-27
Last updated
2024-06-27

Locations

44 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06477237. Inclusion in this directory is not an endorsement.

Study of Efficacy and Safety of HB0017 in Patients With Moderate to Severe Plaque Psoriasis (NCT06477237) · Clinical Trials Directory