49
Participants
Start Date
December 31, 2012
Primary Completion Date
September 30, 2014
Study Completion Date
September 30, 2014
MT-3995 Low
MT-3995 Low dose for 8 weeks
MT-3995 High
MT-3995 High dose for 8 weeks
Placebo
Placebo for 8 weeks
Investigational site, Blagoevgrad
Investigational site, Pazardzhik
Investigational site, Pleven
Investigational site, Plovdiv
Investigational site, Rousse
Investigational site, Sofia
Investigational site, Varna
Investigational site, České Budějovice
Investigational site, Český Krumlov
Investigational site, Karlovy Vary
Investigational site, Ostrava
Investigational site, Ostrava-Vitkovice
Investigational site, Prague
Investigational site, Slaný
Investigational site, Znojmo
Investigational site, Baja
Investigational site, Budapest
Investigational site, Debrecen
Investigational site, Eger
Investigational site, Kistelek
Investigational site, Komárom
Investigational site, Pécs
Investigational site, Szigetvár
Investigational site, Szikszó
Investigational site, Zalaegerszeg
Investigational site, Krakow
Investigational site, Ruda Śląska
Investigational site, Rzeszów
Investigational site, Świętochłowice
Investigational site, Bacau
Investigational site, Brăila
Investigational site, Bucharest
Investigational site, Buzău
Investigational site, Cluj-Napoca
Investigational site, Deva
Investigational site, Iași
Investigational site, Oradea
Investigational site, Ploiesti, Judet Prahova
Investigational site, Satu Mare
Investigational site, Târgu Mureş
Investigational site, Timișoara
Investigational site, Bardejov
Investigational site, Bratislava
Investigational site, Levice
Investigational site, Lučenec
Investigational site, Martin
Investigational site, Nitra
Investigational site, Prešov
Investigational site, Šahy
Investigational site, Štúrovo
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
INDUSTRY