A Study to Evaluate the Efficacy and Safety of LZM012
NCT06110676 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 918
Last updated 2023-11-01
Summary
This study is a muti-center, randomized, double blind, positive control phase III clinical study to evaluate the efficacy and safety of LZM012 in moderate to severe chronic plaque psoriasis patients
Conditions
Interventions
- BIOLOGICAL
-
LZM012
Recombinant anti-human IL-17A/F humanized monoclonal antibody injection
- BIOLOGICAL
-
Secukinumab
Cosentyx
Sponsors & Collaborators
-
Livzon Pharmaceutical Group Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-08-21
- Primary Completion
- 2025-04-30
- Completion
- 2025-06-30
Countries
- China
Study Locations
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