Use of Tocilizumab for Rheumatoid Arthritis (RA) in Daily Routine |
Completed |
Rheumatoid Arthritis |
NCT02809833 |
Tocilizumab in Children With ACP |
Recruiting |
Adamantinomatous Craniopharyngioma |
NCT03970226 |
A Longitudinal Study of ACTEMRA® (Tocilizumab) as Monotherapy in Highly Active NMOSD |
Completed |
Neuromyelitis Optica Spectrum Disorders|Neuromyelitis Optica|Devic's Disease |
NCT03062579 |
EMBRACE-SC: Observational Study of Subcutaneous (SC) Tocilizumab Alone or in Combination With Conventional Disease-Modifying Antirheumatic Drugs (cDMARDs) in Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT02648035 |
A Retrospective Cohort Study on the Risk of Serious Infections in Rheumatoid Arthritis Patients Receiving Tocilizumab |
Not yet recruiting |
Infection|Rheumatoid Arthritis |
NCT04115423 |
Study of the Safety, Tolerability, and Bioactivity of Tocilizumab On Patients With Non-infectious UVEITIS: The STOP-UVEITIS Study |
Unknown status |
Intermediate Uveitis|Posterior Uveitis|Pan-uveitis |
NCT01717170 |
Study of Tocilizumab in Patients With Hepatocellular Carcinoma (HCC) Undergoing Transarterial Chemoembolization (TACE) |
Withdrawn |
Hepatocellular Carcinoma |
NCT02997956 |
Tocilizumab for the Treatment of Refractory Behcet's Uveitis |
Recruiting |
Behcet Syndrome|Uveitis |
NCT03554161 |
An Observational Study of Tocilizumab (Actemra) in Participants With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01741688 |
Itacitinib and Tocilizumab for Steroid Refractory Acute Graft Versus Host Disease |
Not yet recruiting |
Steroid Refractory GVHD|Graft Vs Host Disease |
NCT04070781 |
Tocilizumab Augmentation in Treatment-Refractory Major Depressive Disorder |
Recruiting |
Major Depressive Disorder |
NCT02660528 |
Tocilizumab for Cytokine Release Syndrome Prophylaxis in Haploidentical Transplantation |
Recruiting |
Cytokine Release Syndrome|Stem Cell Transplant Complications |
NCT03533101 |
A Non-Interventional Study of Rheumatoid Arthritis Patients Treated With RoActemra/Actemra (Tocilizumab) in Monotherapy |
Completed |
Rheumatoid Arthritis |
NCT01705730 |
A Non-interventional Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01562327 |
Tocilizumab for Treatment of Steroid Refractory Acute Graft-versus-Host Disease |
Terminated |
Acute Graft Versus Host Disease |
NCT01475162 |
Tocilizumab Plus a Short Prednisone Taper for GCA |
Recruiting |
Giant Cell Arteritis |
NCT03726749 |
Therapeutic Drug Monitoring of Tocilizumab in Rheumatoid Arthritis |
Recruiting |
Rheumatoid Arthritis|Tocilizumab |
NCT03781310 |
An Open-Label Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01951170 |
Single Patient Use of Tocilizumab in Systemic Onset Juvenile Idiopathic Arthritis |
Terminated |
Arthritis, Juvenile Rheumatoid|Still's Disease, Juvenile Onset |
NCT00868751 |
A Time to Cardiovascular Event Analysis Comparing Tocilizumab to Other Biologics in Patients With Rheumatoid Arthritis (RA) |
Unknown status |
Rheumatoid Arthritis |
NCT02797769 |
A Study to Evaluate Pharmacokinetics and Safety of Tocilizumab (RoActemra/Actemra) in Participants Less Than 2 Years Old With Active Systemic Juvenile Idiopathic Arthritis (sJIA) |
Completed |
Juvenile Idiopathic Arthritis |
NCT01455701 |
Tocilizumab as Add-On Treatment For Residual Positive, Negative, and Cognitive Symptoms of Schizophrenia |
Completed |
Schizophrenia|Schizoaffective Disorder |
NCT02034474 |
Pilot Study of Tocilizumab in Patients With Erdheim-Chester Disease |
Terminated |
Erdheim-Chester Disease |
NCT01727206 |
A Study of the Efficacy and Safety of Tocilizumab in Adults With Rheumatoid Arthritis. |
Completed |
Rheumatoid Arthritis |
NCT01988012 |
Tocilizumab for SARS-CoV2 Severe Pneumonitis |
Not yet recruiting |
SARS Pneumonia |
NCT04315480 |
A Study of Subcutaneously Administered Tocilizumab in Participants With Systemic Juvenile Idiopathic Arthritis |
Completed |
Juvenile Idiopathic Arthritis |
NCT01904292 |
Safety and Efficacy of tocilizuMAb Versus Placebo in Polymyalgia rHeumatica With glucocORticoid dEpendence SEMAPHORE |
Active, not recruiting |
Polymyalgia Rheumatica |
NCT02908217 |
An Observational Study of RoActemra/Actemra (Tocilizumab) As Monotherapy in Rheumatoid Arthritis Patients in Routine Clinical Practice |
Completed |
Rheumatoid Arthritis |
NCT01474291 |
Extension Study Evaluating the Safety and Efficacy of Subcutaneous Tocilizumab (RoActemra/Actemra) Administration in Systemic and Polyarticular-Course Juvenile Idiopathic Arthritis |
Active, not recruiting |
Juvenile Idiopathic Arthritis |
NCT02165345 |
An Extension Study to Evaluate Long-Term Safety of Subcutaneous (SC) Tocilizumab in Participants With Giant Cell Arteritis (GCA) |
Completed |
Giant Cell Arteritis |
NCT03202368 |
A Long Term Extension Study of WA19926 (NCT01007435) of Tocilizumab (RoActemra/Actemra) in Participants With Early, Moderate to Severe Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT01668966 |
Tocilizumab vs Azathioprine in Neuromyelitis Optica Spectrum Disorders |
Completed |
Neuromyelitis Optica Spectrum Disorders|Neuromyelitis Optica |
NCT03350633 |
A Long-Term Extension Study to WA19926 (NCT01007435) of Tocilizumab in Participants With Early, Moderate to Severe Rheumatoid Arthritis |
Terminated |
Rheumatoid Arthritis |
NCT01665430 |
Tocilizumab for Relapsing Polychondritis |
Withdrawn |
Relapsing Polychondritis |
NCT01104480 |
Tocilizumab in COVID-19 Pneumonia (TOCIVID-19) |
Recruiting |
COVID-19 Pneumonia |
NCT04317092 |
An Open-Label Trial of Tocilizumab in Schizophrenia |
Completed |
Schizophrenia |
NCT01696929 |
Study of Tocilizumab to Treat Polymyalgia Rheumatica |
Completed |
Polymyalgia Rheumatica (PMR) |
NCT01396317 |
A Long-Term Extension Study of WA19926 on the Safety of Tocilizumab (RoActemra/Actemra) in Participants With Early Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01655381 |
Short-Term Application of Tocilizumab Following Myocardial Infarction |
Completed |
Myocardial Infarction |
NCT02419937 |
Non-Interventional Study of Tocilizumab Subcutaneous (SC) Monotherapy in Participants With Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT02402686 |
Phase I, Pharmacokinetic, Safety and Tolerability Study in Healthy Volunteers |
Completed |
Pharmacokinetics |
NCT03522012 |
Tocilizumab (TCZ) in New-onset Type 1 Diabetes |
Active, not recruiting |
Type 1 Diabetes Mellitus|New-onset Type 1 Diabetes Mellitus|T1DM|T1D |
NCT02293837 |
Tocilizumab and Hemophagocytic Lymphohistiocytosis (HLH) |
Recruiting |
Hemophagocytic Lymphohistiocytosis |
NCT02007239 |
Tocilizumab in Patients With Schnitzler's Syndrome |
Completed |
Schnitzler's Syndrome |
NCT03046381 |
Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate |
Completed |
Rheumatoid Arthritis |
NCT01245452 |
A Study in Patients With Moderate to Severe Active Rheumatoid Arthritis Comparing Different Infusion Durations of RoActemra/Actemra (Tocilizumab) Treatment |
Completed |
Rheumatoid Arthritis |
NCT01468077 |
Effect of Subcutaneous ACTEMRA on Inflamed Atherosclerotic Plaques in Patients With Rheumatoid Arthritis |
Enrolling by invitation |
Rheumatoid Arthritis |
NCT02659150 |
A Study to Evaluate the Efficacy of Tocilizumab as a Remission-Induction and Glucocorticoid-Sparing Regimen in Subjects With New-Onset Polymyalgia Rheumatica (PMR- SPARE) |
Recruiting |
Polymyalgia Rheumatica |
NCT03263715 |
TOSCARA Study: A Study of Subcutaneous Tocilizumab (RoActemra/Actemra) in Participants With Active Rheumatoid Arthritis NaĂŻve to RoActemra/Actemra Treatment |
Completed |
Rheumatoid Arthritis |
NCT02031471 |
Tocilizumab in the Treatment of Refractory Polymyositis and Dermatomyositis |
Completed |
Dermatomyositis|Polymyositis |
NCT02043548 |
A Study of Decreased Dose Frequency in Participants With Systemic Juvenile Arthritis Who Experience Laboratory Abnormalities During Treatment With RoActemra/Actemra (Tocilizumab) |
Completed |
Juvenile Idiopathic Arthritis |
NCT01734382 |
A Long-term Safety Extension Study of Tocilizumab in Brazilian Participants With Rheumatoid Arthritis (RA) Who Completed the Studies ML21530 and MA21488 |
Completed |
Arthritis, Rheumatoid |
NCT01715831 |
A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of Tocilizumab (TCZ) Administered to Participants With Giant Cell Arteritis (GCA). |
Active, not recruiting |
Giant Cell Arteritis |
NCT03923738 |
Tocilizumab in Cardiac Transplantation |
Recruiting |
Heart Transplant |
NCT03644667 |
Tocilizumab for the Treatment of Behcet's Syndrome |
Terminated |
Behcet Syndrome |
NCT01693653 |
A Phase IV Study to Evaluate the Effect of Subcutaneous (SC) Tocilizumab Administered to Participants With Rheumatoid Arthritis (RA) Assessed Using Disease Activity Score (DAS28) |
Completed |
Rheumatoid Arthritis |
NCT02534311 |
A Pilot Study in Severe Patients With Takayasu Arteritis. |
Recruiting |
Takayasu Arteritis|Tocilizumab|Adalimumab|Treatment |
NCT04300686 |
Tocilizumab in the Management of Juvenile Idiopathic Arthritis Associated Uveitis |
Terminated |
Juvenile Idiopathic Arthritis Associated Uveitis |
NCT01603355 |
Efficacy and Tolerance of Tocilizumab In Takayasu Arteritis |
Unknown status |
TAKAYASU ARTERITIS |
NCT02101333 |
Filling Bone Erosions: a Longitudinal Multicentric HR-pQCT Study of Subcutaneous Tocilizumab in Rheumatoid Arthritis |
Recruiting |
Rheumatoid Arthritis |
NCT02765074 |
Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 |
Recruiting |
Covid-19|SARS|Cytokine Storm|Cytokine Release Syndrome|Tocilizumab |
NCT04306705 |
A Study of Subcutaneous (SC) Tocilizumab (RoActemra/Actemra) in Participants With Active Rheumatoid Arthritis (RA) and Inadequate Response to Disease-Modifying Anti-Rheumatic Drugs (DMARDs) |
Completed |
Rheumatoid Arthritis |
NCT02046616 |
Phase II Study of Tocilizumab for Patients With Glucocorticoid-refractory Acute GVHD After Allogeneic Hematopoetic Stem Cell Transplant (HSCT) |
Terminated |
Glucocorticosteroid Refractory Acute GVHD |
NCT01757197 |
Use of Tocilizumab Drug Levels to Optimize Treatment in RA |
Recruiting |
Rheumatoid Arthritis |
NCT03895879 |
A Non-Interventional Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01670045 |
TOward the Lowest Effective DOse of Abatacept or Tocilizumab |
Active, not recruiting |
Rheumatoid Arthritis |
NCT01557374 |
Tocilizumab (RoActemra) and Tranexamic Acid (Cyklokapron) Used as Adjuncts to Chronic Subdural Hematoma Surgery |
Recruiting |
Chronic Subdural Hematoma |
NCT03353259 |
Single Patient Study to Treat Relapsing Polychondritis With Tocilizumab |
Completed |
Relapsing Polychondritis |
NCT01041248 |
Trastuzumab and Pertuzumab in Combination With Tocilizumab in Subjects With Metastatic HER2 Positive Breast Cancer Resistant to Trastuzumab |
Recruiting |
Breast Cancer |
NCT03135171 |
A Study on Safety and Efficacy of Tocilizumab (RoActemra/Actemra) Alone or in Combination With Non-Biologic Antirheumatics in Participants With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01987479 |
A Trial of Tocilizumab in ALS Subjects |
Completed |
ALS|Amyotrophic Lateral Sclerosis|Lou Gehrig's Disease|Motor Neuron Disease |
NCT02469896 |
A Long-Term Extension Study of WA22762 to Evaluate Safety and Efficacy of Subcutaneous Tocilizumab in Participants With Moderate to Severe Rheumatoid Arthritis (RA). |
Completed |
Rheumatoid Arthritis |
NCT01734993 |
A Study to Evaluate the Use of Glucocorticoids in Combination With Tocilizumab in Daily Clinical Practice |
Active, not recruiting |
Rheumatoid Arthritis |
NCT03291457 |
Uncontrolled Study to Evaluate Efficacy of Tocilizumab in Patients With Moderate or Severe Rheumatoid Arthritis |
Unknown status |
Arthritis, Rheumatoid |
NCT02087696 |
A Safety Study of Tocilizumab to Improve Transplant Rates in Highly Sensitized Patients Awaiting Kidney Transplantation |
Completed |
End Stage Renal Disease (ESRD) |
NCT01594424 |
A Long-term Extension Study of Tocilizumab (Myeloma Receptor Antibody [MRA]) in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00721123 |
A Study of the Efficacy and Safety of Tocilizumab in Participants With Systemic Sclerosis (SSc) |
Completed |
Systemic Sclerosis |
NCT02453256 |
Favipiravir Combined With Tocilizumab in the Treatment of Corona Virus Disease 2019 |
Recruiting |
COVID-19 |
NCT04310228 |
Tocilizumab for Renal Graft Inflammation |
Completed |
Late Complication From Kidney Transplant |
NCT02108600 |
A Study of Tocilizumab (RoActemra/Actemra) in Monotherapy or in Combination With Methotrexate or Other Non-Biologic DMARDs in Participants With Active Rheumatoid Arthritis and an Inadequate Response to Current Non-Biologic DMARD Therapy or the First Anti-TNF Biologic Agent |
Completed |
Rheumatoid Arthritis |
NCT02046603 |
A Study to Evaluate Efficacy of Tocilizumab Administered as Monotherapy or in Combination With Methotrexate and/or Other Disease Modifying Antirheumatic Drugs (DMARDs) in Rheumatoid Arthritis (RA) Participants |
Completed |
Rheumatoid Arthritis |
NCT01941940 |
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 |
Rheumatoid Arthritis |
NCT00996606 |
A Study of RoActemra/Actemra (Tocilizumab) in Adult Patients With Rheumatoid Arthritis (SVOBODA Programme) |
Completed |
Rheumatoid Arthritis |
NCT02010216 |
Evolution of Adipokines and Body Composition in Rheumatoid Arthritis Patients Receiving Tocilizumab Therapy |
Completed |
Arthritis, Rheumatoid |
NCT02843789 |
Tocilizumab Real-Life Human Factors (RLHFs) Validation Study |
Completed |
Rheumatoid Arthritis |
NCT02682823 |
A Study of Tocilizumab in Participants With Active Rheumatoid Arthritis (RA) and an Inadequate Response to Non-Biological Disease-modifying Anti-rheumatic Drugs (DMARDs) |
Completed |
Rheumatoid Arthritis |
NCT01617005 |
Success of Tocilizumab in RA Patients With Remission Induction and Sustained Efficacy After Discontinuation |
Completed |
Rheumatoid Arthritis |
NCT01120366 |
Musculoskeletal Ultrasound in Predicting Early Dose Titration With Tocilizumab |
Completed |
Rheumatoid Arthritis |
NCT01717859 |
Ranibizumab for Edema of the mAcula in Diabetes: Protocol 4 With Tocilizumab: The READ-4 Study |
Withdrawn |
Diabetic Macular Edema |
NCT02511067 |
A Study of Tocilizumab in Combination With an Oral Contraceptive in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01044498 |
An Efficacy and Safety Study of Tocilizumab (RoActemra/Actemra) in Participants With Giant Cell Arteritis (GCA) |
Completed |
Giant Cell Arteritis |
NCT01791153 |
Nivolumab and Tocilizumab for Relapsed Hematological Malignancy Post-allogeneic Transplant |
Recruiting |
Acute Leukemia|Chronic Leukemia|Lymphoma|Myelodysplastic Syndromes |
NCT03588936 |
Tocilizumab for KSHV-Associated Multicentric Castleman Disease |
Active, not recruiting |
Castleman Disease|Castleman's Disease|Giant Lymph Node Hyperplasia |
NCT01441063 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Ankylosing Spondylitis Who Have Failed Treatment With NSAIDs |
Terminated |
Spondylitis, Ankylosing |
NCT01209702 |
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 |
Completed |
Rheumatoid Arthritis |
NCT00810199 |
Tocilizumab in Schizophrenia |
Recruiting |
Schizophrenia|Psychotic Disorders |
NCT02874573 |
A Study of Subcutaneous Tocilizumab as Monotherapy and/or in Combination With Non-Biologic Disease Modifying Anti-Rheumatic Drugs (DMARDs) in Participants With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01941095 |
Mechanistic Studies of B- and T-Cell Function in RA Patients Treated With TNF Antagonists, Tocilizumab, or Abatacept |
Active, not recruiting |
Rheumatoid Arthritis (RA) |
NCT02353780 |
PROACTIVE: Preventing Acute/Chronic GVHD With TocIlizumab Combined With GVHD Prophylaxis Post allogEneic Transplant |
Recruiting |
Hematologic Malignancy |
NCT03699631 |
Efficacy of Tocilizumab for the Treatment of Acute AION Related to GCA |
Not yet recruiting |
Giant Cell Arteritis|Optic Ischaemic Neuropathy |
NCT04239196 |
A Study of RoActemra/Actemra (Tocilizumab) Given Subcutaneously in Combination With Traditional DMARDs in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01232569 |
Comparing the Efficacy of Periarticular Bone Structure in Patients Treated With Either Tocilizumab or Tumor Necrosis Factor Blockers |
Completed |
Rheumatoid Arthritis |
NCT02778789 |
A Study of Tocilizumab in Comparison to Etanercept in Participants With Rheumatoid Arthritis and Cardiovascular Disease Risk Factors |
Completed |
Rheumatoid Arthritis |
NCT01331837 |
The Comparative Study of Intra-articular Injection of Tocilizumab and Compound Betamethasone |
Unknown status |
Rheumatoid Arthritis of Knee |
NCT03215407 |
A Study of Tocilizumab in Patients With Active Polyarticular Juvenile Idiopathic Arthritis |
Completed |
Juvenile Idiopathic Arthritis |
NCT00988221 |
Tocilizumab Dose-tapering and Interruption in Patients With Giant Cell Arteritis Achieving the Clinical Remission. |
Unknown status |
Giant Cell Arteritis |
NCT03244709 |
TOCILIZUMAB IN FIBROUS DYSPLASIA OF BONE |
Completed |
Fibrous Dysplasia of Bone |
NCT01791842 |
Tocilizumab for the Treatment of Familial Mediterranean Fever |
Recruiting |
Familial Mediterranean Fever |
NCT03446209 |
Study of the Tocilizumab Optimization Timing for CART19 Associated Cytokine Release Syndrome |
Active, not recruiting |
Lymphoblastic Leukemia, Acute, Childhood |
NCT02906371 |
Efficacy and Safety of Tocilizumab in Adult's Still Disease |
Unknown status |
Adult's Still Disease |
NCT01002781 |
Study to Evaluate the Safety, Tolerability and Efficacy of Tocilizumab in Participants With Rheumatoid Arthritis (RA) Who Have an Inadequate Response to Non-Biologic Disease Modifying Anti-rheumatic Drugs (DMARDs) and/or Anti-tumor Necrosis Factor (Anti-TNF) Therapy |
Completed |
Rheumatoid Arthritis |
NCT01362062 |
A Study of Tocilizumab (RoActemra/Actemra) Versus Adalimumab in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01119859 |
Tocilizumab for Patients With Giant Cell Arteritis |
Completed |
Giant Cell Arteritis |
NCT01450137 |
A Study of Tocilizumab (RoActemra) in Tocilizumab-Naive Participants With Rheumatoid Arthritis and Inadequate Response to Non-Biologic Disease-Modifying Antirheumatic Drugs (DMARDs) and/or Biologic Therapy |
Completed |
Rheumatoid Arthritis |
NCT02001987 |
A Long-Term Extension Study of WA22763 and NA25220 of Subcutaneous RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01772316 |
Local, Non-Interventional Study of RoActemra (Tocilizumab) in Poland (ACT-POL): First-Line Treatment in Routine Clinical Practice of Participants With Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT02234960 |
Ultrasound as Imaging Biomarker of Early Response to Tocilizumab and Methotrexate in Very Early Rheumatoid Arthritis |
Unknown status |
Rheumatoid Arthritis |
NCT02837146 |
Tocilizumab for Chronic Graft-versus-Host Disease Treatment |
Withdrawn |
Graft Versus Host Disease |
NCT02174263 |
A Study of Tocilizumab (RoActemra/Actemra) in Patients With Ankylosing Spondylitis Who Have Had an Inadequate Response to Previous Tumor Necrosis Factor (TNF) Antagonist Therapy |
Terminated |
Spondylitis, Ankylosing |
NCT01209689 |
Study of Nab-Paclitaxel and Gemcitabine With or Without Tocilizumab in Pancreatic Cancer Patients |
Recruiting |
Unresectable Pancreatic Carcinoma |
NCT02767557 |
An Extension Study of Tocilizumab (Myeloma Receptor Antibody [MRA]) in Patients Completing Treatment in Tocilizumab Core Studies |
Completed |
Rheumatoid Arthritis |
NCT00720798 |
Effect of the Interleukin-6 Receptor Antagonist Tocilizumab in Patients With Hand Osteoarthritis |
Completed |
Hand Osteoarthritis |
NCT02477059 |
Evaluation of Tocilizumab as an add-on Therapy to Corticoids in Giant Cell Arteritis: Proof of Concept Study. |
Completed |
Giant Cell Arteritis |
NCT01910038 |
A Prospective Observational Study of Tocilizumab (RoActemra/Actemra) in Participants With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01462162 |
A Study to Evaluate Tocilizumab Treatment in a Real-Life Setting |
Completed |
Rheumatoid Arthritis |
NCT01664104 |
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 |
Rheumatoid Arthritis |
NCT00883753 |
Feasibility of the Combination of Chemotherapy (Carbo/Caelyx or Carbo/Doxorubicin) With Tocilizumab (mAb IL-6R) and Peg-Intron in Patients With Recurrent Ovarian Cancer |
Completed |
Recurrent Ovarian Cancer |
NCT01637532 |
A Non-Interventional Study Evaluating Rheumatoid Arthritis Participants Treated With Tocilizumab (RoActemra/Actemra) |
Completed |
Rheumatoid Arthritis |
NCT01671059 |
A Study of Tocilizumab in Chinese Participants With Systemic Juvenile Idiopathic Arthritis (sJIA) |
Recruiting |
Juvenile Idiopathic Arthritis |
NCT03301883 |
Tocilizumab Treatment in Graves´ Ophthalmopathy (Graves´ Orbitopathy or Thyroid Eye Disease) |
Completed |
Thyroid Associated Ophthalmopathies|Graves´ Ophthalmopathy|Thyroid Eye Disease |
NCT01297699 |
A Study to Compare Subcutaneous Versus Intravenous Administration of RoActemra/Actemra (Tocilizumab) in Participants With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01194414 |
A Phase II Study of the Interleukin-6 Receptor Inhibitor Tocilizumab in Combination With Ipilimumab and Nivolumab in Patients With Unresectable Stage III or Stage IV Melanoma |
Recruiting |
Melanoma |
NCT03999749 |
Study to Compare the Efficacy of Tocilizumab With or Without Glucocorticoid Discontinuation in Rheumatoid Arthritis Participants |
Completed |
Rheumatoid Arthritis |
NCT02573012 |
Effect of the Interleukin-6 Receptor Antagonist Tocilizumab in Non-ST Elevation Myocardial Infarction |
Completed |
Non-ST Elevation Myocardial Infarction |
NCT01491074 |
Alemtuzumab or Tocilizumab in Combination With Etoposide and Dexamethasone for the Treatment of Adult Patients With Hemophagocytic Lymphohistiocytosis |
Recruiting |
Leukemia |
NCT02385110 |
Single-dose Study to Describe the Safety of Sarilumab and Tocilizumab in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT02404558 |
A Therapeutic Open Label Study of Tocilizumab in the Treatment of Pulmonary Arterial Hypertension |
Completed |
Pulmonary Arterial Hypertension |
NCT02676947 |
An Efficacy and Safety Study of Subcutaneous Tocilizumab in Combination With Methotrexate (MTX) and as Monotherapy Versus MTX in Participants With Moderate to Severe Rheumatoid Arthritis With Inadequate Response to Current Disease-Modifying Antirheumatic Drug (DMARD) Therapy |
Recruiting |
Rheumatoid Arthritis |
NCT03155347 |
A Study Evaluating the Safety of Tocilizumab in Addition to Standard of Care Premedication Given Before Obinutuzumab + Chlorambucil in Participants With Untreated B-Cell Chronic Lymphocytic Leukemia (B-CLL) and Comorbidities |
Terminated |
B-Cell Chronic Lymphocytic Leukemia |
NCT02336048 |
Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01579006 |
A Study of Tocilizumab as Monotherapy and in Combination With Methotrexate Versus Methotrexate in Patients With Early Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01007435 |
Efficacy of Tocilizumab in Primary Sjögren's Syndrome. |
Completed |
Primary Sjögren's Syndrome (pSS) |
NCT01782235 |
A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Juvenile Idiopathic Arthritis Who Completed WA19977 Core Study |
Completed |
Juvenile Idiopathic Arthritis |
NCT01667471 |
Effect of Monoclonal Anti-IL6 Antibody (Tocilizumab) on the Cardiovascular Risk in Patients With Rheumatoid Arthritis |
Unknown status |
Rheumatoid Arthritis |
NCT01752335 |
A Study of RoActemra/Actemra (Tocilizumab) Versus Adalimumab in Combination With Methotrexate (MTX) in Patients With Moderate to Severe Active Rheumatoid Arthritis And an Inadequate Response to Treatment With Only One Tumor Necrosis Factor (TNF)-Inhibitor |
Terminated |
Rheumatoid Arthritis |
NCT01283971 |
A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Juvenile Idiopathic Arthritis From France Who Completed WA19977 Core Study |
Completed |
Juvenile Idiopathic Arthritis |
NCT01673919 |
Efficacy and Safety Study of RoActemra (Tocilizumab) in Participants With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT02721004 |
Abatacept vs Tocilizumab for the Treatment of RA in TNF Alpha Inhibitor Inadequate Responders |
Recruiting |
Arthritis, Rheumatoid |
NCT03227419 |
Immunoregulatory Mechanisms of Treg Cells Induced by Tocilizumab |
Completed |
Arthritis,Rheumatoid |
NCT02963402 |
A Study With Tocilizumab [RoActemra/Actemra] Monotherapy or in Combination With Methotrexate in Patients With Rheumatoid Arthritis (PICTURE) |
Completed |
Rheumatoid Arthritis |
NCT01063062 |
A Long-Term Extension Study of WA22762 and NA25220 of Subcutaneous (SC) Tocilizumab (TCZ) in Moderate to Severe Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT01662063 |
A Study to Assess Efficacy With Respect to Clinical Improvement in Disease Activity and Safety of Tocilizumab in Patients Wtih Active Rheumatoid Arthritis. |
Completed |
Rheumatoid Arthritis |
NCT00754559 |
A Study of Tocilizumab in Combination With DMARDs in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00531817 |
A Study of the Effect of Tocilizumab on Markers of Atherogenic Risk in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00535782 |
Tocilizumab REMission in Early RA |
Completed |
Rheumatoid Arthritis |
NCT04157010 |
Tocilizumab Effect iN pOlymyalgia Rheumatica |
Completed |
Polymyalgia Rheumatica |
NCT01713842 |
A Study of Tocilizumab With or Without Methotrexate in Patients With Rheumatoid Arthritis. |
Completed |
Rheumatoid Arthritis |
NCT01010503 |
A Long-Term Extension Study of RoActemra/Actemra (Tocilizumab) in Patients With Early Moderate to Severe Rheumatoid Arthritis Who Completed Study WA19926 |
Completed |
Rheumatoid Arthritis |
NCT01730456 |
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) |
Completed |
Rheumatoid Arthritis |
NCT00891020 |
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) |
Completed |
Rheumatoid Arthritis |
NCT00106535 |
A Study to Evaluate the Safety and Efficacy of Tocilizumab in Patients With Severe COVID-19 Pneumonia |
Not yet recruiting |
COVID-19 Pneumonia |
NCT04320615 |
Randomized Trial Comparing Efficacy of Adalimumab, Anakinra and Tocilizumab in Non-infectious Refractory Uveitis |
Unknown status |
Uveitis|Biotherapy |
NCT02929251 |
Extension Study of Tocilizumab Long Term Treatment of Moderate to Severe Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT01347983 |
An Open-label Study With Tocilizumab in Patients With Rheumatoid Arthritis in a Local Environment |
Completed |
Rheumatoid Arthritis |
NCT01254331 |
An Extension Study of WA19926 of the Long-Term Safety of RoActemra/Actemra (Tocilizumab) in Patients With Early Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01664598 |
Giant Cell Arteritis Treatment With Ultra-short Glucocorticoids and Tocilizumab |
Recruiting |
Giant Cell Arteritis |
NCT03745586 |
An Extension Long-Term Study of RoActemra/Actemra (Tocilizumab) in Patients With Polyarticular Juvenile Idiopathic Arthritis Who Completed The WA19977 Study |
Completed |
Juvenile Idiopathic Arthritis |
NCT01727986 |
Study of Tocilizumab in Combination With Methotrexate for Treatment of Moderate to Severe Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis (RA) |
NCT01258712 |
A Study of Administration of RoActemra/Actemra (Tocilizumab) by Auto-injector Vs. Pre-filled Syringe in Healthy Volunteers |
Completed |
Healthy Volunteer |
NCT01418989 |
Effect of Tocilizumab to the Cellular Immune Response to Influenza Vaccine |
Unknown status |
Rheumatoid Arthritis|Cellular Immune Response |
NCT01980836 |
Study to Describe Real World Drug Retention Rate of the Tocilizumab at One Year |
Completed |
Rheumatoid Arthritis |
NCT02608112 |
To Evaluate 1 Year Extension Study of the Efficacy and Safety of Tocilizumab in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01256736 |
A Study of RoActemra/Actemra (Tocilizumab) Versus Placebo in Patients With Systemic Sclerosis |
Completed |
Sclerosis, Systemic |
NCT01532869 |
A Study of the Effects of RoActemra/Actemra on Vaccination in Patients With Rheumatoid Arthritis on Background Methotrexate (VISARA) |
Completed |
Rheumatoid Arthritis |
NCT01163747 |
A Study of Subcutaneously (SC) Administered Tocilizumab (TCZ) in Participants With Polyarticular-Course Juvenile Idiopathic Arthritis (pJIA) |
Completed |
Juvenile Idiopathic Arthritis |
NCT01904279 |
Phase II Open-Label Trial of Tacrolimus/Methotrexate and Tocilizumab for the Prevention of Acute Graft-Versus-Host Disease After Allogeneic Hematopoietic Stem Cell Transplantation |
Completed |
Hematopoietic Stem Cell Transplantation |
NCT02206035 |
An Observational Study on RoActemra/Actemra (Tocilizumab) in Clinical Practice in Patients With Rheumatoid Arthritis (TRUST) |
Completed |
Rheumatoid Arthritis |
NCT01394276 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis Who Have an Inadequate Response to DMARDs or Anti-TNF |
Completed |
Rheumatoid Arthritis |
NCT01326962 |
A Non-Interventional Study in Rheumatoid Arthritis Patients Treated With Tocilizumab (RoActemra/Actemra) |
Completed |
Rheumatoid Arthritis |
NCT01613378 |
Comparative Study to Evaluate the Pharmacokinetics of BAT1806 vs Actemra® in Healthy Subjects |
Active, not recruiting |
Rheumatoid Arthritis |
NCT03606876 |
Request for Single Patient IND for Compassionate/Emergency Use of Tocilizumab |
No longer available |
Juvenile Idiopathic Arthritis |
NCT00862758 |
A Study of Tocilizumab Added to DMARDs in Patients With Moderate to Severe Rheumatoid Arthritis and an Inadequate Response to DMARDs. |
Completed |
Rheumatoid Arthritis |
NCT00996203 |
An Observational Study to Evaluate the Clinical Effectiveness, Quality of Life, Safety and Tolerability of Tocilizumab (TCZ) in Patients With Rheumatoid Arthritis (RA) in Daily Clinical Practice |
Completed |
Rheumatoid Arthritis |
NCT02552940 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to DMARDs (REMISSION) |
Completed |
Rheumatoid Arthritis |
NCT01610791 |
A Study of the Effects of RoActemra/Actemra (Tocilizumab) on Neutrophils in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to Biologic and/or Non-biologic DMARDs. |
Completed |
Rheumatoid Arthritis |
NCT01195272 |
TARGET GCAT Registry |
Recruiting |
Giant Cell Arteritis |
NCT04049071 |
A Pharmacodynamic Study to Evaluate Neutrophil Distribution Kinetics and Function Following Single-Dose RoActemra/Actemra (Tocilizumab) in Healthy Volunteers |
Completed |
Healthy Volunteer |
NCT01991990 |
Characterization of Non-Steroidal Anti-Inflammatory Drug (NSAID) Intake in Rheumatoid Arthritis (RA) Participants on Tocilizumab (RoACTEMRA®) Treatment |
Completed |
Rheumatoid Arthritis |
NCT03112213 |
MEthotrexate Versus TOcilizumab for Treatment of GIant Cell Arteritis: a Multicenter, Randomized, Controlled Trial |
Recruiting |
Giant Cell Arteritis |
NCT03892785 |
A Study of The Effect of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate on Articular Damage in The Hand in Patients With Moderate to Severe Rheumatoid Arthritis Who Have an Inadequate Response to Non-Biological DMARDs |
Withdrawn |
Rheumatoid Arthritis |
NCT01878318 |
Observational Study of Tocilizumab in Participants With Rheumatoid Arthritis in Australia |
Completed |
Rheumatoid Arthritis |
NCT01683604 |
Ipilimumab, Nivolumab, Tocilizumab and Radiation in Pretreated Patients With Advanced Pancreatic Cancer |
Not yet recruiting |
Pancreatic Cancer |
NCT04258150 |
A Study Comparing Infusion Rates of Tocilizumab in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00887341 |
Regulation of the Immune System in Response to the Treatment With Tocilizumab in Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT01633346 |
A Study to Assess the Effect of Tocilizumab on Signs and Symptoms in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00848120 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01245439 |
A Study to Provide RoActemra/Actemra (Tocilzumab) to Patients With Multicentric Castleman's Disease Who Demonstrated Benefit From Previous RoActemra/Actemra Treatment |
Completed |
Castleman's Disease |
NCT01183598 |
A Study of Tocilizumab in Patients With Rheumatoid Arthritis Who Have an Inadequate Response to Current Non-Biologic DMARDs |
Completed |
Rheumatoid Arthritis |
NCT00810277 |
A Study of RoActemra/Actemra (Tocilizumab) Plus DMARDs in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01214733 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Monotherapy in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01669902 |
A Study of Tocilizumab as Monotherapy or in Combination With DMARDs in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01089023 |
A Study Assessing the Safety and Efficacy of Subcutaneous RoActemra/Actemra Alone or in Combination With Non-biologic Antirheumatics in Rhuematoid Arthritis Patients in Latin America With Inadequate Response to Non-biologic Antirheumatic Drugs. |
Completed |
Rheumatoid Arthritis |
NCT02011334 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Active Rheumatoid Arthritis Who Have an Inadequate Response to Current Non-Biologic and/or Biologic DMARDS |
Completed |
Rheumatoid Arthritis |
NCT01149057 |
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 |
Completed |
Rheumatoid Arthritis |
NCT00977106 |
Characterization of the Effect of Tocilizumab in Vivo and in Vitro on T Follicular Helper Cells in Rheumatoid Arthritis Patients and Consequence on B Cells Maturation |
Completed |
Arthritis, Rheumatoid|Tocilizumab|T-Lymphocytes, Helper-Inducer |
NCT02569736 |
A Non-Interventional Study in Patients With Moderate to Severe Rheumatoid Arthritis Treated With RoActemra/Actemra (Tocilizumab) |
Completed |
Rheumatoid Arthritis |
NCT01663506 |
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. |
Completed |
Rheumatoid Arthritis |
NCT00750880 |
A Study of Glucocorticoid Use to Evaluate Systematic Methylprednisolone Reduction in Patients With Rheumatoid Arthritis on Background RoActemra/Actemra (Tocilizumab) (ACT-ALONE) |
Completed |
Rheumatoid Arthritis |
NCT01219933 |
A Study of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate in Patients With Severe Active Rheumatoid Arthritis, Comparing Tapering Versus Maintaining the Methotrexate Dosage |
Terminated |
Rheumatoid Arthritis |
NCT01661140 |
A Study to Evaluate the Bioequivalence of Tocilizumab Following Subcutaneous Administration Via an Autoinjector (AI 1000-G2) Versus a Pre-Filled Syringe in Healthy Volunteers |
Completed |
Healthy Volunteer |
NCT02678988 |
IL-6 Regulation of Substrate Metabolism and Influence of Obesity |
Recruiting |
Obesity|Healthy |
NCT03967691 |
Efficacy and Safety of Tocilizumab in Combination With DMARDs in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01211834 |
A Study of the Impact of Methotrexate (MTX) Discontinuation on the Efficacy of Subcutaneous (SC) Tocilizumab (TCZ) With MTX |
Completed |
Rheumatoid Arthritis |
NCT01855789 |
Effects of Interleukin-6 Inhibition on Vascular, Endothelial and Left Ventricular Function in Rheumatoid Arthritis |
Recruiting |
Rheumatoid Arthritis|Inflammation |
NCT03288584 |
A Study of Tocilizumab in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01187563 |
A Study of Tocilizumab + DMARDs in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00951275 |
A Drug Interaction Study Between Tocilizumab, Methotrexate and Simvastatin on Patients With Rheumatoid Arthritis. |
Completed |
Rheumatoid Arthritis |
NCT00365001 |
Multicenter, Post-marketing, Non-interventional, Observational Study in RA Patients Treated With RoActemra/Actemra (Tocilizumab) |
Completed |
Rheumatoid Arthritis |
NCT02101307 |
A Study of Tocilizumab and Methotrexate in Combination or as Monotherapy in Treatment-NaĂŻve Patients With Early Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01034137 |
A Study of Tocilizumab in Combination With DMARD Therapy in Patients With Active Rheumatoid Arthritis. |
Completed |
Rheumatoid Arthritis |
NCT00773461 |
Longitudinal Changes in Donor-Derived Cell-Free DNA With Tocilizumab Treatment for Chronic Antibody-Mediated Rejection |
Enrolling by invitation |
Rejection Chronic Renal|Kidney Transplant Rejection |
NCT03859388 |
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 |
Rheumatoid Arthritis |
NCT01353859 |
A Study of RoActemra/Actemra (Tocilizumab) in Combination With DMARDs Versus Current Best Practice DMARD Therapy in Patients With Rheumatoid Arthritis |
Terminated |
Rheumatoid Arthritis |
NCT01251120 |
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 (SARIL-RA-ASCERTAIN) |
Completed |
Rheumatoid Arthritis |
NCT01768572 |
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 |
Completed |
Rheumatoid Arthritis |
NCT00754572 |
A Non-Interventional Study of RoActemra/Actemra (Tocilizumab) Treatment in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01952509 |
A Study of Subcutaneous RoActemra/Actemra (Tocilizumab) as Monotherapy or in Combination With Methotrexate or Other Non-Biologic DMARDs in Patients With Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01995201 |
A Non-Interventional Study in Patients With Rheumatoid Arthritis Who Are Treated With RoActemra/Actemra (Tocilizumab) |
Withdrawn |
Rheumatoid Arthritis |
NCT01893255 |
A Non-Interventional Study of RoActemra/Actemra (Tocilizumab) in Monotherapy in Patients With Rheumatoid Arthritis (MONACO) |
Terminated |
Rheumatoid Arthritis |
NCT01643863 |
An Observational Study in Rheumatoid Arthritis Patients Treated With RoActemra/Actemra (Tocilizumab) |
Completed |
Rheumatoid Arthritis |
NCT01565122 |
A Study to Assess the Safety and Efficacy of Tocilizumab in Patients With Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00109408 |
Tocilizumab Effect on microRNA Expression and Adipokine Levels in Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT03149796 |
Study of Tocilizumab (RoActemre) Administered Subcutaneously in Participants With Rheumatoid Arthritis in Everyday Clinical Practice |
Active, not recruiting |
Rheumatoid Arthritis |
NCT02251860 |
Lymphocyte and Cytokine Disturbances in Polymyalgia Rheumatica |
Completed |
Polymyalgia Rheumatica |
NCT02888496 |
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 |
Rheumatoid Arthritis |
NCT01235507 |
A Study to Assess the Effect of Tocilizumab + DMARD Therapy on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00106574 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT01615419 |
A Study of RoActemra/Actemra and, if Initially Inadequately Responded to RoActemra/Actemra, Followed by MabThera/Rituxan in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01332994 |
The Durability of Early RA Disease Control After Tocilizumab Withdrawal: A Canadian Experience |
Withdrawn |
Rheumatoid Arthritis |
NCT03109470 |
An Extension Study to WA19977 in Patients With Active Polyarticular-Course Juvenile Idiopathic Arthritis |
Terminated |
Juvenile Idiopathic Arthritis |
NCT01575769 |
A Study of Tocilizumab Plus Non-biological DMARD in Patients With Moderate to Severe Rheumatoid Arthritis and an Inadequate Response to Non-biological DMARDs |
Completed |
Rheumatoid Arthritis |
NCT01034397 |
An Observational Study of the Impact of RoActemra/Actemra on Fatigue in Patients With Rheumatoid Arthritis (PEPS) |
Completed |
Rheumatoid Arthritis |
NCT01185522 |
A Long-Term Safety Extension Study of WA19926 in Participants With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01649804 |
A Study of Subcutaneously Administered Tocilizumab in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00965653 |
A Study of RoActemra/Actemra (Tocilizumab) in Patients With Active Systemic Juvenile Idiopathic Arthritis (JIA) |
Completed |
Juvenile Idiopathic Arthritis |
NCT00642460 |
A Retrospective Observational Study on Compliance in Patients With Rheumatoid Arthritis on Treatment With RoActemra/Actemra (Tocilizumab) in Clinical Practice (REMISSION II) |
Completed |
Rheumatoid Arthritis |
NCT01649817 |
A Study to Assess the Effect of Tocilizumab + Methotrexate on Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00106548 |
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 |
Rheumatoid Arthritis |
NCT01587989 |
A Study of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate Versus RoActemra/Actemra Monotherapy in Patients With Rheumatoid Arthritis and an Inadequate Response to Methotrexate |
Completed |
Rheumatoid Arthritis |
NCT01399697 |
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 |
Completed |
Rheumatoid Arthritis |
NCT00106522 |
Pharmacokinetics/Pharmacodynamics (PK/PD) Equivalence Study of MSB11456 |
Completed |
Healthy |
NCT03282851 |
A Prospective, Non-Interventional Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01770834 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Combination With Methotrexate in Patients With Rheumatoid Arthritis (ACTIVATE) |
Completed |
Rheumatoid Arthritis |
NCT01384461 |
Mild-Intensity Whole Body Hyperthermia (WBH) for Major Depressive Disorder |
Not yet recruiting |
Major Depressive Disorder |
NCT03787290 |
An Observational Study of RoActemra/Actemra in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01375478 |
An Global Comparative Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01543503 |
A Study of the Efficacy and Safety of Tocilizumab for Confirmed Rheumatoid Arthritis (RA) Participants in Clinical Practice |
Terminated |
Rheumatoid Arthritis |
NCT02616328 |
An Observational Study on Fatigue in Patients With Rheumatoid Arthritis Treated With RoActemra/Actemra (Tocilizumab) |
Completed |
Rheumatoid Arthritis |
NCT01667458 |
Tocilizumab for the Prevention of Graft Versus Host Disease After Cord Blood Transplantation |
Recruiting |
Acute Myeloid Leukemia|Acute Lymphoblastic Leukemia|Acute Leukemia|Myelodysplastic Syndromes|Myelodysplastic-Myeloproliferative Diseases|Myeloproliferative Disorder|Non Hodgkin Lymphoma|Hodgkin Lymphoma|Leukemia |
NCT03434730 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis |
Terminated |
Rheumatoid Arthritis |
NCT01277328 |
Monitoring Epstein-Barr Virus (EBV) Load in Rheumatoid Arthritis Patients Treated With New Immunosuppressive Drugs |
Unknown status |
Rheumatoid Arthritis |
NCT00947492 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis Who Have an Inadequate Response to DMARDs |
Completed |
Rheumatoid Arthritis |
NCT01388309 |
An Observational Study on Long-Term Effectiveness and Safety of RoActemra/Actemra (Tocilizumab) in Daily Practice in Patients With Rheumatoid Arthritis (ICHIBAN) |
Unknown status |
Rheumatoid Arthritis |
NCT01194401 |
A Non-Interventional Study of RoActemra/Actemra in Patients With Moderate to Severe Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01672970 |
ASSessing the Effect of Anti-IL-6 Treatment in Myocardial Infarction: The ASSAIL-MI Trial |
Active, not recruiting |
Coronary Disease|Myocardial Infarction |
NCT03004703 |
Single-dose Study to Describe the Pharmacodynamics (PD) and Safety of Sarilumab (REGN88/SAR153191) and Tocilizumab in Adults With Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT02097524 |
A Study of Combination Treatment With MabThera (Rituximab) and RoActemra (Tocilizumab) Versus RoActemra in Patients With Rheumatoid Arthritis With an Incomplete Response to Methotrexate |
Terminated |
Rheumatoid Arthritis |
NCT00845832 |
Cell Therapy for Immunomodulation in Kidney Transplantation |
Recruiting |
Kidney Transplantation |
NCT03867617 |
Checkpoint Inhibitor Induced Colitis and Arthritis -Immunomodulation With IL-6 Blockade and Exploration of Disease Mechanisms |
Recruiting |
Solid Tumor|Colitis|Arthritis |
NCT03601611 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis Treated With Glucocorticoids |
Completed |
Rheumatoid Arthritis |
NCT01564901 |
An Observational Study of Glucocorticoid Use in Patients With Rheumatoid Arthritis on Treatment With RoActemra/Actemra (Tocilizumab) |
Completed |
Rheumatoid Arthritis |
NCT01392001 |
IL-6 Inhibition for Modulating Inflammation After Cardiac Arrest |
Active, not recruiting |
Heart Arrest|Out-Of-Hospital Cardiac Arrest|Systemic Inflammatory Response Syndrome |
NCT03863015 |
Rheumatoid Arthritis Treatment After First Anti-TNF INvestiGation |
Recruiting |
Rheumatoid Arthritis |
NCT03100253 |
An Observational Study of RoActemra/Actemra (Tocilizumab) in Smoking Versus Non-Smoking Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01337388 |
ARMONIA: An Observational Study of Biologic Drugs in Monotherapy or Combination With DMARDs in Italian Clinical Practice and the Efficacy and Safety of RoActemra/Actemra (Tocilizumab) Monotherapy in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01791205 |
A Comparative Study to Observe the Effect of Concomitant Use of Corticosteroid Treatment in Rheumatoid Arthritis (RA) Participants Who Are Treated With a Tumor Necrosis Factor (TNF) Inhibitor or Tocilizumab (TCZ) as Their Second Biological Treatment. |
Completed |
Rheumatoid Arthritis |
NCT02679001 |
Ectopic Adipose Tissue, Exercise Training and IL-6 |
Unknown status |
Adiposity |
NCT02901496 |
Evaluation of the BRADA and ABILHAND Questionnaires |
Completed |
Rheumatoid Arthritis |
NCT00938444 |
Anti-il6 Treatment of Serious COVID-19 Disease With Threatening Respiratory Failure |
Not yet recruiting |
Corona Virus Disease |
NCT04322773 |
Evaluation of Desensitization Protocols in HLA-incompatible Kidney-transplant Candidates |
Recruiting |
End-stage Renal Disease|Kidney Transplantation|Hla-incompatible Kidney Transplant Candidates |
NCT03507348 |
AIDS 347: IL-6 Blockade in Treated HIV Infection |
Active, not recruiting |
HIV Infections |
NCT02049437 |
Rotation or Change of Biotherapy After First Anti-TNF Treatment Failure for Rheumatoid Arthritis |
Unknown status |
Rheumatoid Arthritis |
NCT01000441 |
A Retrospective, Observational Study of RoActemra/Actemra (Tocilizumab) in Clinical Practice in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01921478 |
U-Act-After: An Observational Study on Long-Term Efficacy of Tight Control RoActemra/Actemra (Tocilizumab) and/or Methotrexate in Patients With Early Rheumatoid Arthritis Who Have Participated in the U-Act-Early Study (ML22497) |
Completed |
Rheumatoid Arthritis |
NCT01918267 |
An Observational Study on Long-Term Efficacy and Safety of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis (FAct) |
Completed |
Rheumatoid Arthritis |
NCT01483326 |
Study of MRA for Polyarticular Juvenile Idiopathic Arthritis (pJIA) |
Completed |
Systemic Juvenile Idiopathic Arthritis |
NCT00144664 |
An Observational Study of Dosage Patterns in Routine Clinical Practice in Patients With Rheumatoid Arthritis (ACT-LIFE) |
Completed |
Rheumatoid Arthritis |
NCT01338545 |
A Dose Escalation Study of RO7082859 as a Single Agent and in Combination With Obinutuzumab, Administered After a Fixed, Single Pre-Treatment Dose of Obinutuzumab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma |
Recruiting |
Non-Hodgkin's Lymphoma |
NCT03075696 |
Anti-Biopharmaceutical Immunization: Prediction and Analysis of Clinical Relevance to Minimize the Risk of Immunization in Rheumatoid Arthritis Patients or Juvenile Idiopathic Arthritis Patients |
Unknown status |
Rheumatoid Arthritis|Juvenile Idiopathic Arthritis |
NCT02116504 |
Treg Modulation With CD28 and IL-6 Receptor Antagonists |
Recruiting |
Living-Donor Kidney Transplant|Kidney Transplant Recipients |
NCT04066114 |
Korean College of Rheumatology Biologics Registry |
Recruiting |
Rheumatoid Arthritis|Ankylosing Spondylitis|Psoriatic Arthritis |
NCT01965132 |
A Trial of Mosunetuzumab (BTCT4465A) as Consolidation Therapy in Participants With Diffuse Large B-Cell Lymphoma Following First-Line Immunochemotherapy and as Therapy in Participants With Previously Untreated Diffuse Large B-Cell Lymphoma Who Are Unable to Tolerate Full-Dose Chemotherapy |
Recruiting |
Diffuse Large B-cell Lymphoma |
NCT03677154 |
An Open-Label Phase lB Study of RO7082859 and Atezolizumab or Polatuzumab Vedotin in Adult Patients With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma |
Recruiting |
Non-Hodgkins Lymphoma |
NCT03533283 |
Role of Interleukin-6 in Exercise |
Completed |
Diabetes Mellitus, Type 2|Obesity |
NCT01073826 |
Allogeneic Stem Cell Transplantation for Patients With Multiple Myeloma |
Withdrawn |
Multiple Myeloma|Myeloma-Multiple |
NCT02447055 |
Treatment Tapering in JIA With Inactive Disease |
Active, not recruiting |
Juvenile Idiopathic Arthritis |
NCT02840175 |
Comparative Study of BAT1806 to RoActemra® in Rheumatoid Arthritis Patients With Inadequate Response to Methotrexate |
Recruiting |
Rheumatoid Arthritis |
NCT03830203 |
Dose Reduction for Early Rheumatoid Arthritis Patients With Low Disease Activity |
Recruiting |
Rheumatoid Arthritis |
NCT02466581 |
A Phase IIb Study for ALX-0061 Monotherapy in Subjects With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT02287922 |
Impact of Acute and Chronic Inflammation on Cytochromes P450 Activity Measured With Dried Blood Spot |
Unknown status |
Inflammation |
NCT03262051 |
Phaseâ…˘Open-label Study of MRA for Rheumatoid Arthritis(RA) |
Completed |
Rheumatoid Arthritis |
NCT00380601 |
Study of MRA in Patients With Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT00144651 |
Long-term Treatment Study of MRA for Polyarticular Juvenile Idiopathic Arthritis (pJIA) |
Completed |
Polyarticular Juvenile Idiopathic Arthritis |
NCT00144625 |
Long-term Treatment Study of MRA for Systemic Juvenile Idiopathic Arthritis (sJIA) |
Completed |
Systemic Juvenile Idiopathic Arthritis |
NCT00144612 |
Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA220JP or MRA221JP |
Completed |
Rheumatoid Arthritis |
NCT00144586 |
Clinical Pharmacology Study of MRA in Patient With Rheumatoid Arthritis (RA) With Renal Impairment |
Completed |
Rheumatoid Arthritis |
NCT00144573 |
Drug-Drug Interaction Study of MRA in Patient With Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT00144560 |
Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA012JP |
Completed |
Rheumatoid Arthritis |
NCT00144547 |
Long-term Treatment Study of MRA for Rheumatoid Arthritis (RA) From Study MRA213JP |
Completed |
Rheumatoid Arthritis |
NCT00144534 |
A Study of Duration of Maintained Efficacy in Rheumatoid Arthritis (RA) Patients Off Treatment With MRA(a Development Code of Tocilizumab, an Anti IL-6 Receptor Monoclonal Antibody.) |
Completed |
Rheumatoid Arthritis |
NCT00661284 |
Development and Analysis of a Stool Bank for Cancer Patients |
Recruiting |
Carcinoma, Non-Small-Cell Lung|Carcinoma, Colorectal |
NCT04291755 |
Allogeneic or Haploidentical Stem Cell Transplant Followed By High-Dose Cyclophosphamide in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia |
Terminated |
Leukemia, Myeloid, Acute |
NCT02057770 |
Usefulness of Non TNF Usage in RA Patients |
Recruiting |
Rheumatoid Arthritis |
NCT03784261 |
A Randomized, Multi-Center Biomarker Trial to Predict Therapeutic Responses of Patients With Rheumatoid Arthritis to a Specific Biologic Mode of Action |
Completed |
Rheumatoid Arthritis |
NCT01638715 |
The Registry Study of Takayasu Arteritis in East China |
Recruiting |
Takayasu Arteritis|Mechanisms, Defense|Pregnancy Related|Treatment Refusal|Outcome |
NCT03893136 |
Modified Immune Cells (CD19/CD20 CAR-T Cells) in Treating Patients With Recurrent or Refractory B-Cell Lymphoma or Chronic Lymphocytic Leukemia |
Recruiting |
CD19 Positive|CD20 Positive|Recurrent Chronic Lymphocytic Leukemia|Recurrent Diffuse Large B-Cell Lymphoma|Recurrent Follicular Lymphoma|Recurrent Mantle Cell Lymphoma|Recurrent Primary Mediastinal (Thymic) Large B-Cell Cell Lymphoma|Recurrent Small Lymphocytic Lymphoma|Refractory Chronic Lymphocytic Leukemia|Refractory Diffuse Large B-Cell Lymphoma|Refractory Follicular Lymphoma|Refractory Mantle Cell Lymphoma|Refractory Primary Mediastinal (Thymic) Large B-Cell Cell Lymphoma|Refractory Small Lymphocytic Lymphoma |
NCT04007029 |
A Study of RO7172508 in Patients With Locally Advanced and/or Metastatic CEA-Positive Solid Tumors |
Completed |
Solid Tumors |
NCT03539484 |
Clinical Trial Evaluating Methotrexate + Biologic Versus Methotrexate, Salazopyrine and Hydroxychloroquine in Patients With Rheumatoid Arthritis and Insufficient Response to Methotrexate |
Unknown status |
Rheumatoid Arthritis|Insufficient Response to Methotrexate. |
NCT02714634 |
A Study of RO6958688 in Participants With Locally Advanced and/or Metastatic Carcinoembryonic Antigen Positive Solid Tumors |
Completed |
Solid Tumors |
NCT02324257 |
Active Conventional Therapy Compared to Three Different Biologic Treatments in Early Rheumatoid Arthritis With Subsequent Dose Reduction |
Active, not recruiting |
Rheumatoid Arthritis |
NCT01491815 |
A Study Comparing Biologics + Methotrexate With Biologics + Tacrolimus in Patients With Rheumatoid Arthritis (RA) |
Recruiting |
Rheumatoid Arthritis (RA) |
NCT03737708 |
CD19 T-CAR for Treatment of Children and Young Adults With r/r B-ALL |
Recruiting |
B-cell Acute Lymphoblastic Leukemia|Acute Lymphocytic Leukemia, Pediatric |
NCT03467256 |
Evaluation Effects of Treatment With IL-6R Inhibitor on Clinical Response and Biomarkers in Patients With Rheumatoid Arthritis (RA) Not Responding to DMARDs and/or a First Biological Agent. |
Unknown status |
Rheumatoid Arthritis (RA) |
NCT01835613 |
Personalized Targeted Preparative Regimen Before T-depleted Allogeneic HSCT in Children With Chemoresistent Acute Leukemias |
Not yet recruiting |
Refractory Acute Myeloid Leukemia|Refractory Acute Lymphoblastic Leukemia |
NCT04000698 |
Study of MRA for Systemic Juvenile Idiopathic Arthritis (sJIA) |
Completed |
Systemic Juvenile Idiopathic Arthritis |
NCT00144599 |
Phase III Comparative Study(Open-Label) of MRA for Rheumatoid Arthritis(RA) |
Completed |
Rheumatoid Arthritis |
NCT00144508 |
the Bispecific PSMAxCD3 Antibody CC-1 in Patients With Castration Resistant Prostate Carcinoma |
Recruiting |
Castration-Resistant Prostatic Cancer |
NCT04104607 |
A Phase Ib Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Cibisatamab in Combination With Atezolizumab After Pretreatment With Obinutuzumab in Participants With Previously Treated Metastatic Colorectal Adenocarcinoma |
Active, not recruiting |
Colorectal Cancer |
NCT03866239 |
Metoprolol for the Treatment of Cytokine Release Syndrome in Patients Treated With Chimeric Antigen Receptor T Cells |
Recruiting |
Solid Tumor|Hematologial Malignancy |
NCT04082910 |
A Study of RO7082859 in Combination With Rituximab or Obinutuzumab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Participants With Non-Hodgkin Lymphomas and Participants With DLBCL |
Recruiting |
B-Cell Lymphoma|Non-Hodgkin Lymphoma |
NCT03467373 |
Ustekinumab for the Treatment of Relapse of Refractory Giant Cell Arteritis |
Recruiting |
Patients Relapsing Refractory Giant Cell Arteritis |
NCT03711448 |
A Retrospective Observational Study on the Use of Biologics in Monotherapy in Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01834807 |
Efficacy and Safety of CDP6038 in Patients With Rheumatoid Arthritis With an Unsuccessful Response to Anti-Tumor Necrosis Factor (Anti-TNF) Therapy |
Completed |
Rheumatoid Arthritis |
NCT01242488 |
A Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-based Treatment Combinations in Patients With Locally Advanced or Metastatic Urothelial Carcinoma After Failure With Platinum-Containing Chemotherapy |
Recruiting |
Urothelial Carcinoma |
NCT03869190 |
Clinical and Immunogenetic Characterization of Giant Cell Arteritis (GCA) and Polymyalgia Rheumatica (PMR) |
Recruiting |
Giant Cell Arteritis|Polymyalgia Rheumatica |
NCT04102930 |
Biomarkers in Rheumatoid Arthritis Treated With Anti-interleukin-6 Therapy |
Recruiting |
Rheumatoid Arthritis |
NCT04281602 |
Impact of the Persistence of Inflammation at Doppler Ultrasound Level on the Structural Evolution of Erosion in Rheumatoid Arthritis Treated With Biotherapy |
Completed |
Rheumatoid Arthritis |
NCT02531061 |
Study of Refractory and/or Relapsing TAkayasu aRTeritis |
Recruiting |
Systemic Vasculitis|Arteritis, Takayasu|Arteritis |
NCT03543527 |
Abatacept in earLy Onset Polymyalgia Rheumatica: Study ALORS |
Recruiting |
Polymyalgia Rheumatica |
NCT03632187 |
Ultrasound and Withdrawal of Biological DMARDs in Rheumatoid Arthritis |
Recruiting |
Rheumatoid Arthritis |
NCT01602302 |
Using Adalimumab Serum Concentration to Choose a Subsequent Biological DMARD in Rheumatoid Arthritis Patients Failing Adalimumab Treatment |
Recruiting |
Rheumatoid Arthritis |
NCT04251741 |
Depression and Anxiety in Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis|Depression|Anxiety |
NCT02122406 |
Cardiovascular Risk and Chronic Inflammatory Rheumatism |
Recruiting |
Rheumatology|Cardiovascular Diseases|Arthritis, Rheumatoid|Spondyloarthritis |
NCT03187444 |
Effects of Antirheumatic Treatment on Levels of Survivin in Rheumatoid Arthritis Patients |
Recruiting |
Rheumatoid Arthritis |
NCT03440892 |
A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Mosunetuzumab + Lenalidomide, RO7082859 + Lenalidomide, and RO7082859 + Lenalidomide + Obinutuzumab in Participants With Relapsed or Refractory Follicular Lymphoma |
Not yet recruiting |
Follicular Lymphoma |
NCT04246086 |
A Study to Evaluate the Safety and Efficacy of Mosunetuzumab (BTCT4465A) in Combination With Polatuzumab Vedotin in B-Cell Non-Hodgkin Lymphoma |
Recruiting |
B-cell Non-Hodgkin Lymphoma |
NCT03671018 |
Comparative Study (Double-Blind) of MRA for Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT00144521 |
RETRO (REduction of Therapy in RA Patients in Ongoing Remission) |
Unknown status |
Rheumatoid Arthritis |
NCT02779114 |
An Observational Study in Clinical Practice Management of Patients With Biological Drugs in Monotherapy |
Completed |
Rheumatoid Arthritis |
NCT01664117 |
A Phase Ib/II Study Investigating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Mosunetuzumab (BTCT4465A) in Combination With CHOP or CHP-Polatuzumab Vedotin in Participants With B-Cell Non-Hodgkin Lymphoma |
Recruiting |
B-cell Non-Hodgkin Lymphoma |
NCT03677141 |
A Study Of Multiple Immunotherapy-Based Treatment Combinations In Participants With Metastatic Non-Small Cell Lung Cancer (Morpheus- Non-Small Cell Lung Cancer) |
Recruiting |
Carcinoma, Non-Small-Cell Lung |
NCT03337698 |
Anti-CD19 CAR-T Cells With Inducible Caspase 9 Safety Switch for B-cell Lymphoma |
Recruiting |
Lymphoma|Lymphoma, B-Cell|Immune System Diseases|Immunoproliferative Disorders|Lymphatic Diseases |
NCT03696784 |
Predicting Hospitalized Infection in Patients With Chronic Inflammatory Arthritis Treated With Biological Drugs |
Completed |
Rheumatoid Arthritis|Spondyloarthritis|Psoriatic Arthritis |
NCT03496831 |
Study of Tisagenlecleucel in Chinese Pediatric and Young Adult Subjects With Relapsed or Refractory B-cell ALL |
Not yet recruiting |
B-cell Acute Lymphoblastic Leukemia |
NCT04156659 |
An Open-label Extension Study of Canakinumab in Patients With Systemic Juvenile Idiopathic Arthritis and Active Systemic Manifestations Manifestations and Response Characterization Study in Canakinumab Treatment-naĂŻve Patients With Active SJIA With and Without Fever. |
Completed |
Systemic Juvenile Idiopathic Arthritis |
NCT00891046 |
A Retrospective Chart Review on the Use of Biologics in Monotherapy for the Treatment of Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01640548 |
An Observational Study to Describe in Routine Clinical Practice the Treatment Patterns of Usage of Biological DMARDs in RA Patients. |
Completed |
Rheumatoid Arthritis |
NCT02590562 |
Comparative Analysis of Outcomes Among Patients Initiating Xeljanz in Combination With Oral MTX Who Withdraw MTX Versus Continue MTX |
Completed |
Rheumatoid Arthritis |
NCT03975790 |
Pragmatic Clinical Trials in Scleroderma |
Not yet recruiting |
Scleroderma, Systemic|Sclerosis, Systemic |
NCT03610217 |
Enhancing Patient Ability to Understand and Utilize Complex Information Concerning Medication Self-management |
Completed |
Rheumatoid Arthritis |
NCT02820038 |