An Open-label, Rollover Study Providing Continued Dosing of Gevokizumab in Order to Assess Long-term Gevokizumab Safety Data



Status:Terminated
Conditions:Cervical Cancer, Ocular
Therapuetic Areas:Oncology, Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:March 2014
End Date:December 2017

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An Open-Label, Non-Randomized, Single-Arm, Rollover Study to Continue Dosing of Gevokizumab in Subjects With Non Infectious Intermediate-, Posterior-, or Pan-Uveitis Patients Who Each Successfully Completed Either the X052130/CL3-78989-005 (EYEGUARD™-A) or the X052131/CL3-78989-006 (EYEGUARD™-C) Study or Who Have Controlled Ocular Inflammation After Receiving Study Drug in Study X052133 (EYEGUARD™-US)

The purpose of this study is to provide continued dosing of gevokizumab in order to obtain
and assess long-term gevokizumab safety data.


Inclusion Criteria:

- Completed either the X052130/CL3-78989-005 or the X052131/CL3-78989-006 study's
masked D392 or OL-224 completion day visits or had controlled ocular inflammation
after having received study drug in Part 2 of study X052133

Exclusion Criteria:

- Discontinued from the previous study

Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
33
sites
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Waltham, MA
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Baltimore, MD
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Belmont, NC
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Beverly Hills, California 90211
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Beverly Hills, CA
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Bloomfield, NJ
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Bridgeport, CT
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Cambridge, MA
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Chandler, AZ
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Charlotte, North Carolina 28207
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Charlotte, NC
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Chicago, IL
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Dallas, TX
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Ellsworth, ME
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Fargo, ND
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Golden, CO
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Houston, TX
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Indianapolis, IN
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Jackson, MI
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Lakeland, FL
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Littleton, CO
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Norfolk, VA
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Omaha, NE
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Phoenix, AZ
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Redlands, CA
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Riverside, CA
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Royal Oak, MI
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Sacramento, CA
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Salt Lake City, UT
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San Antonio, TX
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Santa Ana, CA
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Tampa, FL
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Teaneck, NJ
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Victorville, CA
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Winston-Salem, NC
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