Trials / Terminated
TerminatedNCT02258854
An Open-label, Rollover Study Providing Continued Dosing of Gevokizumab in Order to Assess Long-term Gevokizumab Safety Data
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)
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 69 (actual)
- Sponsor
- XOMA (US) LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to provide continued dosing of gevokizumab in order to obtain and assess long-term gevokizumab safety data.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dose 2 gevokizumab | Solution for subcutaneous injection |
Timeline
- Start date
- 2014-03-01
- Primary completion
- 2017-10-01
- Completion
- 2017-12-01
- First posted
- 2014-10-08
- Last updated
- 2015-10-16
Locations
33 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02258854. Inclusion in this directory is not an endorsement.