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Trials / Completed

CompletedNCT04914429

A Study of Guselkumab (TREMFYA) in Chinese Participants With Moderate to Severe Plaque Psoriasis

A Phase 4, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Guselkumab (TREMFYA) in Chinese Participants With Moderate to Severe Plaque Psoriasis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
327 (actual)
Sponsor
Janssen Research & Development, LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of guselkumab in the treatment of Chinese participants with moderate to severe plaque psoriasis.

Conditions

Interventions

TypeNameDescription
DRUGGuselkumabGuselkumab 100 mg will be administered as a SC injection.
DRUGPlaceboMatching placebo will be administered as a SC injection.

Timeline

Start date
2021-08-25
Primary completion
2023-09-26
Completion
2023-09-26
First posted
2021-06-04
Last updated
2023-10-12

Locations

26 sites across 1 country: China

Source: ClinicalTrials.gov record NCT04914429. Inclusion in this directory is not an endorsement.

A Study of Guselkumab (TREMFYA) in Chinese Participants With Moderate to Severe Plaque Psoriasis (NCT04914429) · Clinical Trials Directory