A Study to Evaluate the Efficacy and Safety of LZM012

NCT06110676 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 918

Last updated 2023-11-01

No results posted yet for this study

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

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06110676 on ClinicalTrials.gov