Clinical Trials Directory

Trials / Completed

CompletedNCT02349451

A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122 in Subjects With Active Psoriatic Arthritis (PsA) Who Have an Inadequate Response to Methotrexate (MTX)

A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122 in Subjects With Active Psoriatic Arthritis Who Have an Inadequate Response to Methotrexate

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
240 (actual)
Sponsor
AbbVie · Industry
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

This study is a Phase 2 randomized, double-blind, double-dummy, active- and placebo-controlled, parallel-group study designed to assess the safety, tolerability, efficacy, pharmacokinetics and immunogenicity of multiple doses of ABT-122 in participants with active PsA who are inadequately responding to MTX treatment.

Conditions

Interventions

TypeNameDescription
BIOLOGICALadalimumab
BIOLOGICALABT-122

Timeline

Start date
2015-04-28
Primary completion
2016-07-04
Completion
2016-07-04
First posted
2015-01-28
Last updated
2017-08-04
Results posted
2017-08-04

Source: ClinicalTrials.gov record NCT02349451. Inclusion in this directory is not an endorsement.