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Efficacy and Safety Study of Apremilast to Treat Active Psoriatic Arthritis

NCT01172938 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 504

Last updated 2020-06-19

Study results available
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Summary

The purpose of this study is to determine whether apremilast is safe and effective in the treatment of patients with psoriatic arthritis, specifically in improving signs and symptoms of psoriatic arthritis (tender and swollen joints, pain, physical function) in treated patients.

Conditions

Interventions

DRUG

Apremilast 20mg

Apremilast 20 mg twice daily, orally

DRUG

Apremilast 30mg

Apremilast 30 mg twice daily, orally

DRUG

Placebo + 20 mg Apremilast

Placebo + 20 mg Apremilast

DRUG

Placebo + 30 mg Apremilast

Placebo + 30 mg Apremilast

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-06-02
Primary Completion
2012-04-27
Completion
2016-10-27

Countries

  • United States
  • Australia
  • Austria
  • Canada
  • France
  • Germany
  • Hungary
  • New Zealand
  • Poland
  • Russia
  • South Africa
  • Spain
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT01172938 on ClinicalTrials.gov