This study will evaluate the long term safety and efficacy of pregabalin (Lyrica) when administered by itself (without any other anti-epileptic medication) to epilepsy patients for the treatment of partial seizures. This is an extension study to a previous clinical trial.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
75
pregabalin
Seizure Frequency
Time frame: Baseline up to Week 28
Number of Participants With (All Causality) Adverse Events (AEs) and Serious Adverse Events (SAEs)
Counts of participants who had treatment-emergent adverse events (TEAEs), defined as newly occurring or worsening after first dose. Participants with multiple occurrences of an AE within a category were counted once within the category.
Time frame: Baseline up to Week 28
Number of Participants With Laboratory Test Values of Potential Clinical Importance
Pre-defined criteria were established for each laboratory test (hematology, blood chemistry and urinalysis) to define the values that would be identified as of potential clinical importance.
Time frame: Baseline up to Week 28
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Pfizer Investigational Site
Phoenix, Arizona, United States
Pfizer Investigational Site
Fayetteville, Arkansas, United States
Pfizer Investigational Site
Fullerton, California, United States
Pfizer Investigational Site
Long Beach, California, United States
Pfizer Investigational Site
Modesto, California, United States
Pfizer Investigational Site
Murrieta, California, United States
Pfizer Investigational Site
Newport Beach, California, United States
Pfizer Investigational Site
Temecula, California, United States
Pfizer Investigational Site
Denver, Colorado, United States
Pfizer Investigational Site
Jacksonville, Florida, United States
...and 34 more locations