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Open Label Continuation Study in Moderate to Severe Psoriasis

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AbbVie

Status and phase

Completed
Phase 3

Conditions

Moderate to Severe Plaque Psoriasis

Treatments

Drug: ABT-874

Study type

Interventional

Funder types

Industry

Identifiers

NCT00626002
M10-016
2007-005955-40 (EudraCT Number)

Details and patient eligibility

About

The purpose of this study is to evaluate long term safety, efficacy and tolerability of ABT-874 in adults with moderate to severe psoriasis.

Enrollment

2,301 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having participated in a preceding ABT-874 clinical trial for ABT-874
  • Subject has a clinical diagnosis of moderate to severe plaque psoriasis

Exclusion criteria

  • Subjects who prematurely discontinued in any preceding psoriasis study with ABT-874 other than protocol-required discontinuation

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

2,301 participants in 1 patient group

1
Experimental group
Treatment:
Drug: ABT-874

Trial contacts and locations

152

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Data sourced from clinicaltrials.gov

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