Efficacy and Safety of Olokizumab With Rheumatoid Arthritis With Previously Failed to Anti-tumor Necrosis Factor (Anti-TNF) Therapy

PHASE2CompletedINTERVENTIONAL
Enrollment

119

Participants

Timeline

Start Date

October 31, 2011

Primary Completion Date

February 28, 2013

Study Completion Date

February 28, 2013

Conditions
Rheumatoid Arthritis
Interventions
BIOLOGICAL

Placebo

Placebo solution for injection, administered as subcutaneous injections

BIOLOGICAL

Olokizumab 60 mg

Olokizumab 60 mg solution for injection, administered as subcutaneous injections

BIOLOGICAL

Olokizumab 120 mg

Olokizumab 120 mg solution for injection, administered as subcutaneous injections

BIOLOGICAL

Olokizumab 240 mg

Olokizumab 240 mg solution for injection, administered as subcutaneous injections

Trial Locations (39)

Unknown

102, Chiba

114, Fukuoka

115, Fukuoka

113, Hiroshima

120, Kakogawa

118, Kumamoto

116, Kurume

121, Matsuyama

122, Matsuyama

107, Nagaoka

110, Nagoya

103, Narita

112, Okayama

119, Ōita

100, Sapporo

117, Sasebo

124, Tokorozawa

123, Tokyo

101, Tomakomai

108, Tonami

111, Tsu

105, Yokohama

104, Yotukaido

200, Daejeon

201, Junggu

202, Seongdong-gu

203, Seoul

204, Seoul

303, Changhua

304, Dalin-Town

305, Hualien City

300, Kaohsiung City

301, Taichung

306, Taichung

307, Taichung

302, Taipei

308, Taipei

309, Taipei

310, Taipei

All Listed Sponsors
lead

UCB Japan Co. Ltd.

INDUSTRY

NCT01463059 - Efficacy and Safety of Olokizumab With Rheumatoid Arthritis With Previously Failed to Anti-tumor Necrosis Factor (Anti-TNF) Therapy | Biotech Hunter | Biotech Hunter