Viewing Study NCT03536884



Ignite Creation Date: 2024-05-06 @ 11:29 AM
Last Modification Date: 2024-10-26 @ 12:46 PM
Study NCT ID: NCT03536884
Status: COMPLETED
Last Update Posted: 2023-09-28
First Post: 2018-05-14

Brief Title: A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
Sponsor: UCB Biopharma SRL
Organization: UCB Pharma

Study Overview

Official Title: A Multicenter Randomized Double-Blind Secukinumab-Controlled Parallel-Group Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: BE RADIANT
Brief Summary: This is a study to compare the efficacy of bimekizumab versus secukinumab in subjects with moderate to severe chronic plaque psoriasis PSO
Detailed Description: The study consists of a 48-week double-blind Treatment Period an optional 96-week open-label extension OLE Period and an optional 48-week OLE2 Period for eligible subjects in the USA and Canada

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2017-003784-35 EUDRACT_NUMBER None None