A Clinical Study to Investigate the Long-term Use of Lacosamide as Monotherapy in Subjects Who Completed Study SP0994

PHASE3CompletedINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

January 31, 2016

Primary Completion Date

January 31, 2020

Study Completion Date

January 31, 2020

Conditions
Epilepsy
Interventions
DRUG

Lacosamide

"* Pharmaceutical Form: Oral tablets~* Concentration: 50 mg~* Route of Administration: Oral administration"

Trial Locations (46)

Unknown

Sp1042 805, Blagoevgrad

Sp1042 807, Pazardzhik

Sp1042 811, Sofia

Sp1042 205, Helsinki

Sp1042 207, Kuopio

Sp1042 236, Nancy

Sp1042 263, Altenburg

Sp1042 265, Bad Neustadt an der Saale

Sp1042 269, Leipzig

Sp1042 256, Marburg

Sp1042 259, Osnabrück

Sp1042 831, Asaka

Sp1042 834, Kagoshima

Sp1042 844, Kamakura

Sp1042 835, Nagoya

Sp1042 837, Okayama

Sp1042 847, Sapporo

Sp1042 751, Riga

Sp1042 547, San Luis Potosí City

Sp1042 672, Pasig

Sp1042 676, Quezon

Sp1042 340, Katowice

Sp1042 342, Lublin

Sp1042 343, Warsaw

Sp1042 576, Bucharest

Sp1042 570, Iași

Sp1042 572, Târgu Mureş

Sp1042 387, Kazan'

Sp1042 389, Kazan'

Sp1042 401, Moscow

Sp1042 392, Novosibirsk

Sp1042 397, Saint Petersburg

Sp1042 400, Saint Petersburg

Sp1042 521, Daegu

Sp1042 518, Daejeon

Sp1042 517, Seoul

Sp1042 519, Seoul

Sp1042 440, Gothenburg

Sp1042 442, Linköping

Sp1042 438, Stockholm

Sp1042 651, Aarau

Sp1042 654, Biel

Sp1042 653, Lugano

Sp1042 622, Chernihiv

Sp1042 626, Kharkiv

Sp1042 625, Odesa

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

UCB Biopharma S.P.R.L.

INDUSTRY