Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 827 in Subjects With Psoriasis



Status:Terminated
Conditions:Psoriasis
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - Any
Updated:10/14/2017
Start Date:April 2010
End Date:September 2015

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A Long-term Assessment of the Safety and Efficacy of AMG 827 Subcutaneous Treatment in Subjects With Psoriasis

This study is an open-label extension of study 20090062 to evaluate extended subcutaneous
dosing of AMG 827 for up to 362 weeks.


Inclusion Criteria:

- Subject was randomized into Study 20090062 and completed the week 16 evaluation.

Exclusion Criteria:

- Subject had any Serious Adverse Event (SAE) reported during Study 20090062 that was
considered possibly related to IP.

- Subject experienced an adverse event in Study 20090062 that, in the opinion of the
investigator, could cause extension of treatment to be detrimental to the subject.
We found this trial at
7
sites
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Dallas, TX
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Albuquerque, NM
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Kogarah,
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Newnan, GA
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Skokie, IL
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St. Louis, MO
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Webster, TX
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