A Study to Look at the Efficacy and Safety of Keppra® Extended Release Formulation - XR

PHASE3CompletedINTERVENTIONAL
Enrollment

158

Participants

Timeline

Start Date

August 31, 2006

Primary Completion Date

May 31, 2007

Study Completion Date

May 31, 2007

Conditions
Epilepsy
Interventions
DRUG

Keppra® extended release formulation - XR

500mg extended release oral tablet, 2 tablets once daily

DRUG

Placebo

oral tablets, 2 tablets once daily

Trial Locations (34)

Unknown

N01235 1007, Curitiba

N01235 2001, Kuopio

N01235 2003, Tampere

N01235 2002, Turku

N01235 3008, Chennai

N01235 3010, Chennai

N01235 3012, Gandhinagar

N01235 3003, Hyderabad

N01235 3004, Hyderabad

N01235 3001, Lucknow

N01235 3009, Madurai

N01235 3002, Mumbai

N01235 3007, Mumbai

N01235 3011, Visakhapatnam

N01235 4006, Aguascalientes

N01235 4003, Distrio Federal

N01235 4001, Guadalajara

N01235 4005, Puebla City

N01235 5001, Moscow

N01235 5002, Moscow

N01235 5003, Moscow

N01235 5005, Moscow

N01235 5006, Moscow

N01235 5007, Moscow

N01235 5004, Saint Petersburg

N01235 5009, Saint Petersburg

N01235 5008, Smolensk

N01235 6002, Cape Town

N01235 6003, Umhlanga

N01235 7001, Kharkiv

N01235 7004, Kharkiv

N01235 7005, Lviv

N01235 7002, Odesa

N01235 7003, Poltava

Sponsors

Lead Sponsor

All Listed Sponsors
lead

UCB Pharma

INDUSTRY

NCT00368069 - A Study to Look at the Efficacy and Safety of Keppra® Extended Release Formulation - XR | Biotech Hunter | Biotech Hunter