119
Participants
Start Date
July 31, 2011
Primary Completion Date
May 31, 2013
Study Completion Date
May 31, 2013
Lu AA21004
Lu AA21004 10 mg, tablets, orally, once daily for 2 weeks; reduced to 5 mg or increased to 20 mg, once daily if necessary according to the responses and symptoms of participants for up to 50 weeks.
Inzai-shi
Noda
Fukuoka
Kitakyushu-shi
Annaka-shi
Fujioka-shi
Takasaki-shi
Hatsukaichi-shi
Hiroshima
Sapporo
Amagasaki-shi
Kobe
Ibaraki
Fujisawa-shi
Kawasaki-shi
Sagamihara-shi
Yokohama
Osaka
Kumamoto
Kyoto
Kurashiki-shi
Osaka
Fukaya-shi
Saitama
Utsunomiya
Anan-shi
Tokushisma-shi
Hachioji-shi
Katsushika-ku
Musashino-shi
Tokyo
Nanyo-shi
Lead Sponsor
Takeda
INDUSTRY