Clinical Trials Directory

Trials / Terminated

TerminatedNCT01708629

Efficacy and Safety of Brodalumab Compared With Placebo and Ustekinumab in Moderate to Severe Plaque Psoriasis Subjects

A Phase 3 Study to Evaluate the Efficacy and Safety of Induction and Maintenance Regimens of Brodalumab Compared With Placebo and Ustekinumab in Subjects With Moderate to Severe Plaque Psoriasis: AMAGINE-3

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
1,881 (actual)
Sponsor
Bausch Health Americas, Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the safety and efficacy of brodalumab at two different doses compared with placebo in participants with moderate to severe plaque psoriasis. A second purpose of this study is to assess the safety and efficacy brodalumab at two different doses compared with ustekinumab in participants with moderate to severe plaque psoriasis. A third purpose of this study is to assess the safety and efficacy of 4 maintenance regimens of brodalumab.

Detailed description

This study assess the safety and efficacy of brodalumab at two different doses compared with placebo in participants with moderate to severe plaque psoriasis. A second purpose of this study is to assess the safety and efficacy brodalumab at two different doses compared with ustekinumab in participants with moderate to severe plaque psoriasis. A third purpose of this study is to assess the safety and efficacy of 4 maintenance regimens of brodalumab.

Conditions

Interventions

TypeNameDescription
DRUG210 mg brodalumab210 mg brodalumab administered SC
DRUG140 mg brodalumab140 mg brodalumab administered SC
DRUGustekinumab45 mg or 90 mg ustekinumab administered SC per the labeled dosing regimen.
DRUGplaceboplacebo administered SC

Timeline

Start date
2012-09-01
Primary completion
2014-08-01
Completion
2015-10-01
First posted
2012-10-17
Last updated
2020-01-03
Results posted
2020-01-03

Locations

157 sites across 11 countries: United States, Australia, Belgium, Canada, France, Greece, Hungary, Italy, Latvia, Poland, Russia

Source: ClinicalTrials.gov record NCT01708629. Inclusion in this directory is not an endorsement.