A Study of MabThera (Rituximab) in Participants With Rheumatoid Arthritis Who Have Had an Inadequate Response to Disease-Modifying Antirheumatic Drugs (DMARD) and/or Anti-Tumor Necrosis Factor (Anti-TNF) Therapy.

PHASE3CompletedINTERVENTIONAL
Enrollment

215

Participants

Timeline

Start Date

June 30, 2005

Primary Completion Date

May 26, 2013

Study Completion Date

May 26, 2013

Conditions
Rheumatoid Arthritis
Interventions
DRUG

Rituximab [MabThera/Rituxan]

1000 mg IV on days 1 and 15

Trial Locations (16)

16100

EMMS Nazareth; Internal Department A, Nazareth

22100

Nahariya Hospital; Rheumatology Dept, Nahariya

Shaare Zedek Medical Center; Rheumatology Dept, Nahariya

34362

Carmel Hospital; Rheumatology Dept, Haifa

38100

Hillel Yaffe MC; Internal C - Rheumatology, Hadera

44281

Meir Medical Center; Internal Dept A, Kfar Saba

58100

Wolfson Hospital; Rheumatology, Holon

76100

Kaplan Medical Center; Reumatology, Rehovot

78306

Barzilai; Rheumatology, Ashkelon

91240

Hadassah Mount Scopus Hospital; Rheumatology, Jerusalem

3109601

Rambam Medical Center; Rheumatology, Haifa

3339419

Bnei Zion Medical Center; Rheumatology, Haifa

4941492

Beilinson Medical Center; Rheumatology, Petah Tikva

6093000

Assaf Harofe; Dept of Medicine B, Beer Yaakov

6423906

Sourasky / Ichilov Hospital; Rheumatology, Tel Aviv

8410101

Soroka Medical Center; Reumatology, Beersheba

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT00503425 - A Study of MabThera (Rituximab) in Participants With Rheumatoid Arthritis Who Have Had an Inadequate Response to Disease-Modifying Antirheumatic Drugs (DMARD) and/or Anti-Tumor Necrosis Factor (Anti-TNF) Therapy. | Biotech Hunter | Biotech Hunter