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 |
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.
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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