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58 Trials

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Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Actemra IV (tocilizumab) / Roche, JW Pharma
NCT00144612: Long-term Treatment Study of MRA for Systemic Juvenile Idiopathic Arthritis (sJIA)

Completed
3
60
Japan
MRA(Tocilizumab)
Chugai Pharmaceutical
Systemic Juvenile Idiopathic Arthritis
06/05
06/09
NCT00144625: Long-term Treatment Study of MRA for Polyarticular Juvenile Idiopathic Arthritis (pJIA)

Completed
3
19
Japan
MRA(Tocilizumab)
Chugai Pharmaceutical
Polyarticular Juvenile Idiopathic Arthritis
07/05
06/09
NCT00144534: Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA213JP

Completed
3
115
Japan
MRA (Tocilizumab)
Chugai Pharmaceutical
Rheumatoid Arthritis
08/05
06/09
NCT00106535 / 2004-003733-14: A Study to Assess the Effect of Tocilizumab + Methotrexate on Prevention of Structural Joint Damage in Patients With Moderate to Severe Active Rheumatoid Arthritis (RA)

Checkmark ACR-ARHP 2014: Rheumatoid Arthritis (LITHE Biomarker study)
Oct 2014 - Oct 2014: ACR-ARHP 2014: Rheumatoid Arthritis (LITHE Biomarker study)
Checkmark ARA 2014 - Rheumatoid arthritis (LITHE)
Apr 2014 - Apr 2014: ARA 2014 - Rheumatoid arthritis (LITHE)
Checkmark Safety and prevention data in patients with moderate to severe rheumatoid arthritis
More
Completed
3
1196
US, Europe, RoW
tocilizumab [RoActemra/Actemra], RoActemra, Actemra, Placebo, Methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
05/07
07/12
OPTION, NCT00106548: A Study to Assess the Effect of Tocilizumab + Methotrexate on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis

Completed
3
623
Canada, Europe, RoW
tocilizumab [RoActemra/Actemra], Placebo, Methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
 
10/07
RADIATE, NCT00106522: A Study to Assess the Effect of Tocilizumab + Methotrexate on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis Currently on Methotrexate Therapy

Checkmark P3 data
Jul 2012 - Jul 2012: P3 data
Checkmark Data
Mar 2012 - Mar 2012: Data
Completed
3
499
US, Canada, Europe, RoW
Methotrexate, Placebo, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
11/07
11/07
TOWARD, NCT00106574 / 2004-005210-37: A Study to Assess the Effect of Tocilizumab + DMARD Therapy on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis

Checkmark ARA 2014: Rheumatoid arthritis (TOWARD)
Apr 2014 - Apr 2014: ARA 2014: Rheumatoid arthritis (TOWARD)
Checkmark EULAR 2013: Rheumatoid arthritis
May 2013 - May 2013: EULAR 2013: Rheumatoid arthritis
Completed
3
1220
US, Canada, Europe, RoW
Placebo, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
12/07
12/07
LITHE, NCT00109408: A Study to Assess the Safety and Efficacy of Tocilizumab in Patients With Active Rheumatoid Arthritis

Checkmark AMBITION
Feb 2017 - Feb 2017: AMBITION
Checkmark ACR-ARHP 2015: Rheumatoid arthritis (AMBITION)
Oct 2015 - Oct 2015: ACR-ARHP 2015: Rheumatoid arthritis (AMBITION)
Checkmark AMBITION (CRA - AHPA 2014)
More
Completed
3
673
US, Canada, Europe, RoW
Methotrexate, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
12/07
12/07
NCT00144547: Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA012JP

Completed
3
241
Japan
MRA(Tocilizumab)
Chugai Pharmaceutical
Rheumatoid Arthritis
08/08
06/09
NCT00144586: Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA220JP or MRA221JP

Completed
3
42
Japan
MRA(Tocilizumab)
Chugai Pharmaceutical
Rheumatoid Arthritis
08/08
06/09
NCT00380601: PhaseⅢOpen-label Study of MRA for Rheumatoid Arthritis(RA)

Completed
3
20
Japan
MRA(Tocilizumab)
Chugai Pharmaceutical
Rheumatoid Arthritis
08/08
02/09
NCT00535782 / 2007-001114-17: A Study of the Effect of Tocilizumab on Markers of Atherogenic Risk in Patients With Moderate to Severe Rheumatoid Arthritis

Checkmark Data in MEASURE trial on patients with moderate to severe rheumatoid arthritis
Dec 2013 - Dec 2013: Data in MEASURE trial on patients with moderate to severe rheumatoid arthritis
Completed
3
132
US, Canada, Europe
Tocilizumab, RoActemra, Actemra, Placebo, Methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
09/08
01/11
ROSE, NCT00531817: A Study of Tocilizumab in Combination With DMARDs in Patients With Moderate to Severe Rheumatoid Arthritis

Checkmark ROSE
Jan 2013 - Jan 2013: ROSE
Checkmark Data
Sep 2011 - Sep 2011: Data
Completed
3
619
US
Tocilizumab, Actemra, RoActemra, Placebo, Permitted DMARDs
Hoffmann-La Roche
Rheumatoid Arthritis
06/09
03/11
NCT00642460 / 2007-000872-18: A Study of RoActemra/Actemra (Tocilizumab) in Patients With Active Systemic Juvenile Idiopathic Arthritis (JIA)

Checkmark Systemic juvenile idiopathic arthritis - TENDER
Mar 2014 - Mar 2014: Systemic juvenile idiopathic arthritis - TENDER
Checkmark P3 data: SJIA
Dec 2012 - Dec 2012: P3 data: SJIA
Checkmark P3 data - ACR/ARHP 2012 (TENDER) (RA)
More
Completed
3
112
US, Canada, Europe, RoW
tocilizumab [RoActemra/Actemra], Placebo, Non-steroidal anti-inflammatory drugs (NSAIDs), methotrexate, corticosteroids
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
09/09
08/14
NCT00754559 / 2008-000105-11: A Study to Assess Efficacy With Respect to Clinical Improvement in Disease Activity and Safety of Tocilizumab in Patients Wtih Active Rheumatoid Arthritis.

Completed
3
286
Europe
Tocilizumab
Hoffmann-La Roche
Rheumatoid Arthritis
11/09
11/09
NCT00848120: A Study to Assess the Effect of Tocilizumab on Signs and Symptoms in Patients With Rheumatoid Arthritis

Completed
3
29
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
02/10
02/10
NCT00810277 / 2008-004126-16: A Study of Tocilizumab in Patients With Rheumatoid Arthritis Who Have an Inadequate Response to Current Non-Biologic DMARDs

Completed
3
14
Europe
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
05/10
05/10
NCT00891020: A Study Of Tocilizumab in Patients With Moderate to Severe Active Rheumatoid Arthritis Who Have an Inadequate Response to or Are Unable to Tolerate Biologic and Non-Biologic Disease-modifying Antirheumatic Drugs (DMARDs)

Checkmark P3 data - ACR/ARHP 2012 (ACT-STAR) (RA)
Sep 2012 - Sep 2012: P3 data - ACR/ARHP 2012 (ACT-STAR) (RA)
Checkmark P3 data (ACT-STAR) (RA)
Sep 2012 - Sep 2012: P3 data (ACT-STAR) (RA)
Checkmark Data
More
Completed
3
886
US
tocilizumab [RoActemra/Actemra], Nonbiologic DMARDs of investigator's choice
Hoffmann-La Roche
Rheumatoid Arthritis
07/10
03/11
NCT00773461: A Study of Tocilizumab in Combination With DMARD Therapy in Patients With Active Rheumatoid Arthritis.

Completed
3
209
RoW
tocilizumab [RoActemra/Actemra], Placebo
Hoffmann-La Roche
Rheumatoid Arthritis
07/10
07/10
ACT-RAY, NCT00810199 / 2008-001847-20: A Study of Tocilizumab and Methotrexate Treatment Strategies (Adding Tocilizumab to Methotrexate Versus Switching to Tocilizumab) in Patients With Active Rheumatoid Arthritis With Inadequate Response to Prior Methotrexate Treatment

Checkmark ACT-RAY
Aug 2014 - Aug 2014: ACT-RAY
Checkmark EULAR 2014: Rheumatoid Arthritis (ACT-RAY)
May 2014 - May 2014: EULAR 2014: Rheumatoid Arthritis (ACT-RAY)
Checkmark ARA 2014 - Rheumatoid arthritis (ACT-RAY)
More
Completed
3
556
US, Europe, RoW
tocilizumab [RoActemra/Actemra], RoActemra/Actemra, methotrexate, placebo
Hoffmann-La Roche
Rheumatoid Arthritis
08/10
01/13
NCT01211834: Efficacy and Safety of Tocilizumab in Combination With DMARDs in Patients With Moderate to Severe Rheumatoid Arthritis

Completed
3
90
RoW
tocilizumab, DMARDs, Placebo
JW Pharmaceutical
Rheumatoid Arthritis
10/10
10/10
PICTURE, NCT01063062: A Study With Tocilizumab [RoActemra/Actemra] Monotherapy or in Combination With Methotrexate in Patients With Rheumatoid Arthritis

Completed
3
107
RoW
tocilizumab [RoActemra/Actemra], Methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
01/11
01/11
NCT01214733: A Study of RoActemra/Actemra (Tocilizumab) Plus DMARDs in Patients With Rheumatoid Arthritis

Completed
3
30
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
05/11
05/11
NCT00750880 / 2008-000587-17: An Exploratory Study of Tocilizumab in Patients With Active Rheumatoid Arthritis (RA) and an Inadequate Response to Current Non-Biologic DMARDs and/or Anti-TNF Therapy.

Checkmark P3 data - APLAR 2012 (ACT-SURE) (RA)
Sep 2012 - Sep 2012: P3 data - APLAR 2012 (ACT-SURE) (RA)
Checkmark Data - EULAR 2012
Jun 2012 - Jun 2012: Data - EULAR 2012
Checkmark P3b data (ACT-SURE)
More
Completed
3
1681
Canada, Europe, RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
07/11
07/11
NCT00951275 / 2009-011105-17: A Study of Tocilizumab + DMARDs in Patients With Moderate to Severe Active Rheumatoid Arthritis

Completed
3
105
Europe
tocilizumab [RoActemra/Actemra], Standard DMARDs (Disease Modifying Anti Rheumatic Drugs)
Hoffmann-La Roche
Rheumatoid Arthritis
07/11
07/11
NCT01610791: A Study of RoActemra/Actemra (Tocilizumab) in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to DMARDs (REMISSION)

Completed
3
121
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
08/11
08/11
NCT00977106 / 2008-008309-23: TORPEDO Study: A Study on Rapid Effect of Tocilizumab in Patients With Rheumatoid Arthritis With an Inadequate Response to Disease-Modifying Antirheumatic Drugs (DMARDs) or Anti-TNF

Checkmark P3 data - ACR/ARHP 2012 (TORPEDO) (RA)
Sep 2012 - Sep 2012: P3 data - ACR/ARHP 2012 (TORPEDO) (RA)
Completed
3
103
Europe
tocilizumab [RoActemra/Actemra], placebo
Hoffmann-La Roche
Rheumatoid Arthritis
10/11
10/11
NCT00988221 / 2009-011593-15: A Study of Tocilizumab in Patients With Active Polyarticular Juvenile Idiopathic Arthritis

Checkmark
May 2014 - May 2014: 
Checkmark Juvenile idiopathic arthritis - CHERISH
Mar 2014 - Mar 2014: Juvenile idiopathic arthritis - CHERISH
Checkmark ACR/ARHP 2013
More
Completed
3
188
US, Canada, Europe, RoW
Tocilizumab, RoActemra, Actemra, Placebo
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
11/11
01/13
NCT01256736: To Evaluate 1 Year Extension Study of the Efficacy and Safety of Tocilizumab in Patients With Moderate to Severe Rheumatoid Arthritis

Checkmark ACR/ARHP 2013
Sep 2013 - Sep 2013: ACR/ARHP 2013
Completed
3
89
RoW
Tocilizumab, DMARDs
JW Pharmaceutical
Rheumatoid Arthritis
12/11
11/13
NCT01044498: A Study of Tocilizumab in Combination With an Oral Contraceptive in Patients With Rheumatoid Arthritis

Completed
3
46
US
Tocilizumab, RoActemra, Actemra, Ortho-Novum® 1/35
Hoffmann-La Roche
Rheumatoid Arthritis
02/12
02/12
ACT-SURE, NCT00883753 / 2008-006924-68 / ACTRN12609000747224: An Extension to Study MA21573, Evaluating Tocilizumab in Patients With Active Rheumatoid Arthritis and an Inadequate Response to Current Non-Biological DMARDs and/or Anti-tumor Necrosis Factor (TNF) Therapy

Completed
3
934
Canada, Europe, RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche, Roche Products Pty Limited
Patients with severe to moderate rheumatoid arthritis
04/12
04/12
NCT00996606 / 2009-012185-32: A Study of Tocilizumab in Combination With Disease-Modifying Anti-Rheumatic Drugs (DMARDs) in Participants With Moderate to Severe Active Rheumatoid Arthritis With an Inadequate Response to DMARDs

Completed
3
58
Europe
DMARDs, Tocilizumab, RoActemra, Actemra
Hoffmann-La Roche
Rheumatoid Arthritis
04/12
04/12
NCT00721123 / 2005-002423-13: A Long-term Extension Study of Tocilizumab (Myeloma Receptor Antibody [MRA]) in Patients With Rheumatoid Arthritis

Completed
3
538
Canada, Europe, RoW
Tocilizumab, RoActemra, Actemra, Tocilizumab (MRA), TCZ
Hoffmann-La Roche
Rheumatoid Arthritis
05/12
05/12
NCT01007435 / 2009-012759-12: A Study of Tocilizumab as Monotherapy and in Combination With Methotrexate Versus Methotrexate in Patients With Early Moderate to Severe Rheumatoid Arthritis

Checkmark FUNCTION
Oct 2015 - Oct 2015: FUNCTION
Checkmark EULAR 2014: Rheumatoid Arthritis
May 2014 - May 2014: EULAR 2014: Rheumatoid Arthritis
Checkmark EULAR 2013: Rheumatoid arthritis (AMBITION & FUNCTION)
More
Completed
3
1162
US, Canada, Europe, RoW
Tocilizumab, RoActemra, Actemra, Placebo to tocilizumab, Methotrexate, Placebo to methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
05/12
01/14
NCT01353859: A Study of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to Non-biologic DMARDs

Completed
3
39
RoW
tocilizumab [RoActemra/Actemra], methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
07/12
07/12
NCT00754572: A Study to Assess the Effect of Tocilizumab Plus Methotrexate on Safety and Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis

Checkmark ACR-ARHP 2015: Rheumatoid arthritis
Oct 2015 - Oct 2015: ACR-ARHP 2015: Rheumatoid arthritis
Checkmark Data - EULAR 2012 [RITMO]
Jun 2012 - Jun 2012: Data - EULAR 2012 [RITMO]
Completed
3
418
RoW
tocilizumab [RoActemra/Actemra], methotrexate
Hoffmann-La Roche
Rheumatoid Arthritis
10/12
10/12
NCT01258712: Study of Tocilizumab in Combination With Methotrexate for Treatment of Moderate to Severe Rheumatoid Arthritis Patients

Completed
3
86
RoW
Tocilizumab + methotrexate(MTX), Tocilizumab placebo + methotrexate(MTX)
Chugai Pharma Taiwan
Rheumatoid Arthritis (RA)
10/12
10/12
NCT01235507: A Study of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to Disease-Modifying Antirheumatic Drugs (DMARDs) (ALABASTER)

Completed
3
71
RoW
methotrexate, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
12/12
12/12
NCT01254331: An Open-label Study With Tocilizumab in Patients With Rheumatoid Arthritis in a Local Environment

Completed
3
51
RoW
tocilizumab [RoActemra]
Hoffmann-La Roche
Rheumatoid Arthritis
02/13
02/13
NCT01347983: Extension Study of Tocilizumab Long Term Treatment of Moderate to Severe Rheumatoid Arthritis Patients

Completed
3
72
RoW
Tocilizumab+Methotrexate(MTX)
Chugai Pharma Taiwan
Rheumatoid Arthritis
03/13
04/13
NCT00720798 / 2005-002909-23: An Extension Study of Tocilizumab (Myeloma Receptor Antibody [MRA]) in Patients Completing Treatment in Tocilizumab Core Studies

Completed
3
2067
US, Canada, Europe, RoW
Tocilizumab, RoActemra, Actemra, Disease-modifying anti-rheumatic drugs, Non-steroidal anti-inflammatory drugs, Oral corticosteroids
Hoffmann-La Roche
Rheumatoid Arthritis
04/13
04/13
NCT01326962: A Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis Who Have an Inadequate Response to DMARDs or Anti-TNF

Checkmark
May 2016 - May 2016: 
Completed
3
28
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
05/13
05/13
NCT01667471 / 2011-001097-25: A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Juvenile Idiopathic Arthritis Who Completed WA19977 Core Study

Completed
3
6
Europe
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
08/13
08/13
NCT01575769: An Extension Study to WA19977 in Patients With Active Polyarticular-Course Juvenile Idiopathic Arthritis

Terminated
3
41
Europe, RoW
RoActemra/Actemra (tocilizumab)
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
12/13
12/13
NCT01673919: A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Juvenile Idiopathic Arthritis From France Who Completed WA19977 Core Study

Completed
3
7
Europe
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
01/14
01/14
NCT01332994 / 2010-022049-88: A Study of RoActemra/Actemra and, if Initially Inadequately Responded to RoActemra/Actemra, Followed by MabThera/Rituxan in Patients With Rheumatoid Arthritis

Checkmark ACR-ARHP 2014: Rheumatoid Arthritis (MIRAI)
Oct 2014 - Oct 2014: ACR-ARHP 2014: Rheumatoid Arthritis (MIRAI)
Checkmark ACR-ARHP 2014: Rheumatoid Arthritis (MIRAI)
Oct 2014 - Oct 2014: ACR-ARHP 2014: Rheumatoid Arthritis (MIRAI)
Checkmark ACR/ARHP 2013
More
Completed
3
519
Europe
rituximab [MabThera/Rituxan], tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
02/14
02/14
NCT01587989 / 2011-001863-39: A Study of RoActemra/Actemra (Tocilizumab) With or Without Methotrexate in Patients With Mild to Moderate Rheumatoid Arthritis With an Inadequate Response to Methotrexate

Completed
3
77
Europe
methotrexate, placebo, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
02/14
02/14
NCT01245439: A Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis

Completed
3
65
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
08/14
08/14
NCT01034137 / 2009-013316-12: A Study of Tocilizumab and Methotrexate in Combination or as Monotherapy in Treatment-Naïve Patients With Early Rheumatoid Arthritis

Checkmark EULAR 2016
Jun 2016 - Jun 2016: EULAR 2016
Checkmark ACR-ARHP 2015: Rheumatoid arthritis (U-ACT-EARLY)
Oct 2015 - Oct 2015: ACR-ARHP 2015: Rheumatoid arthritis (U-ACT-EARLY)
Completed
3
317
Europe
methotrexate, placebo MTX, placebo TCZ, tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
09/14
09/14
SARIL-RA-ASCERTAIN, NCT01768572 / 2012-003536-23: To Evaluate The Safety of SAR153191 (REGN88) and Tocilizumab Added to Other RA Drugs in Patients With RA Who Are Not Responding to or Intolerant of Anti-TNF Therapy

Checkmark ACR 2015: ASCERTAIN and Study 1309 trials
Nov 2015 - Nov 2015: ACR 2015: ASCERTAIN and Study 1309 trials
Completed
3
202
US, Europe, RoW
sarilumab SAR153191 (REGN88), tocilizumab, hydroxychloroquine, methotrexate, sulfasalazine, leflunomide, subcutaneous placebo, intravenous placebo
Sanofi, Regeneron Pharmaceuticals
Rheumatoid Arthritis
10/14
10/14
NCT01649804 / 2011-006125-14: A Long-Term Safety Extension Study of WA19926 in Participants With Rheumatoid Arthritis

Completed
3
12
Europe
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
12/14
12/14
NCT01665430: A Long-Term Extension Study to WA19926 (NCT01007435) of Tocilizumab in Participants With Early, Moderate to Severe Rheumatoid Arthritis

Terminated
3
38
Europe
Tocilizumab, RoActemra/Actemra
Hoffmann-La Roche
Rheumatoid Arthritis
02/15
02/15
NCT01730456: A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Early Moderate to Severe Rheumatoid Arthritis Who Completed Study WA19926

Completed
3
13
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Rheumatoid Arthritis
05/15
05/15
NCT01664598: An Extension Study of WA19926 of the Long-Term Safety of Tocilizumab (RoActemra/Actemra) in Patients With Early Moderate to Severe Rheumatoid Arthritis

Completed
3
49
RoW
Tocilizumab, RoActemra, Actemra
Hoffmann-La Roche
Rheumatoid Arthritis
06/15
06/15
NCT01655381: A Long-Term Extension Study of WA19926 on the Safety of Tocilizumab (RoActemra/Actemra) in Participants With Early Moderate to Severe Rheumatoid Arthritis

Completed
3
15
Europe
Tocilizumab, RoActemra®, Actemra®
Hoffmann-La Roche
Rheumatoid Arthritis
07/15
07/15
NCT01988012: A Study of the Efficacy and Safety of Tocilizumab in Adults With Rheumatoid Arthritis.

Completed
3
100
RoW
tocilizumab, RoActemra/Actemra
Hoffmann-La Roche
Rheumatoid Arthritis
07/15
07/15
NCT01297699 / 2010-023841-31: Tocilizumab Treatment in Graves´ Ophthalmopathy (Graves´ Orbitopathy or Thyroid Eye Disease)

Completed
3
32
Europe
Tocilizumab (RoActemra®), Sterile 0.9% Sodium Chloride
Hospital Clinico Universitario de Santiago, Fundación Ramón Domínguez
Thyroid Associated Ophthalmopathies, Graves´ Ophthalmopathy, Thyroid Eye Disease
10/15
12/15
NCT01727986: An Extension Long-Term Study of RoActemra/Actemra (Tocilizumab) in Patients With Polyarticular Juvenile Idiopathic Arthritis Who Completed The WA19977 Study

Completed
3
11
RoW
tocilizumab [RoActemra/Actemra]
Hoffmann-La Roche
Juvenile Idiopathic Arthritis
11/15
11/15

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