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Efficacy, Safety, and Withdrawal and Retreatment With Brodalumab in Moderate to Severe Plaque Psoriasis Subjects

NCT01708590 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 661

Last updated 2020-01-03

Study results available
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Summary

The purpose of this study is to assess the safety and efficacy of brodalumab taken every two weeks at two different doses.

Conditions

Interventions

DRUG

210 mg brodalumab

210 mg brodalumab administered subcutaneous (SC)

DRUG

140 mg brodalumab

140 mg brodalumab administered subcutaneous (SC)

DRUG

placebo

Placebo administered subcutaneous (SC)

Sponsors & Collaborators

  • Bausch Health Americas, Inc.

    lead INDUSTRY

Principal Investigators

  • MD · Amgen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2014-05-31
Completion
2015-08-31

Countries

  • United States
  • Canada
  • France
  • Germany
  • Poland
  • Switzerland

Study Locations

More Related Trials

Entities

Drugs
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 NCT01708590 on ClinicalTrials.gov