An Analysis of Peripheral Blood T Cell Subsets on Rheumatoid Arthritis
NCT00555542 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2008-05-09
Summary
To study the effects of T cell in peripheral blood of patients with RA undergoing selective B cell depletion have not been studied. We analyze the B and T cell subsets in patients with active RA treated undergoing this form of treatment with rituximab.
Conditions
Interventions
- DRUG
-
Patients are taking stable dose of methotrexate and at least 10mg folic acid per week for at least 4 weeks. Rituximab is administrated as 1000mg intravenous infusion on day 1 and day 15. Premedication as standard prescription consists of methylprednisolone 100mg IV, Chlorpheniramine maleate(piriton 10mg IV and oral paracetamol 500mg to be given 30 minutes before each infusion of rituximab. Oral prednisolone 60mg is tob e given from day 1-6 after rituximab infusion and 30mg from day 7-13.
Sponsors & Collaborators
-
Chinese University of Hong Kong
lead OTHER
Principal Investigators
-
Edmund Kwok Ming LI, MD · Chinese University of Hong Kong
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-07-31
- Primary Completion
- 2008-05-31
- Completion
- 2008-05-31
Countries
- China
Study Locations
More Related Trials
-
Rituximab-induced Pulmonary Function Changes
NCT01632124 ·Status: UNKNOWN
-
An Open-label Study of GC012F in Rheumatoid Arthritis.
NCT07315503 ·Status: NOT_YET_RECRUITING ·Phase: EARLY_PHASE1
-
Stem Cell Support in Patients With Rheumatoid Arthritis
NCT00278551 ·Status: TERMINATED ·Phase: PHASE1
-
Comparative Effectiveness of Targeted Therapy in RA Patients
NCT04449224 ·Status: UNKNOWN
-
JAK-i on RA B-lymphocytes Tolerance and Disease Resolution Through JAK Signaling In Rheumatoid Arthritis
NCT05754112 ·Status: UNKNOWN
-
An Open-label Extension Study of Certolizumab Pegol in Chinese Patients With Rheumatoid Arthritis Who Enrolled in RA0044
NCT02319642 ·Status: COMPLETED ·Phase: PHASE3
-
Research Study on the Immunosuppressive Effects of a Cell Therapy Product on PBMC Isolated From Blood of Patients With Inflammatory Rheumatic Diseases
NCT03454932 ·Status: TERMINATED
-
A Study of the Safety of Rituximab in Combination With Other Anti-Rheumatic Drugs in Subjects With Active Rheumatoid Arthritis
NCT00443651 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of B-cell Depletion by Rituximab and Anti-CD 19 CAR-T Therapy in Patients With Rheumatoid Arthritis
NCT06475495 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Rituximab in Rheumatoid Arthritis Lung Disease
NCT00578565 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid Arthritis (RA) Who Are on a Stable Dose of Conventional Synthetic Disease-Modifying Anti-Rheumatic Drugs (csDMARDs) and Have an Inadequate Response to csDMARDs
NCT02720523 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
A Study of TJ003234 in Rheumatoid Arthritis Patients
NCT04457856 ·Status: UNKNOWN ·Phase: PHASE1
-
A Study to Evaluate the Effects of Rituximab on Immune Responses in Subjects With Active Rheumatoid Arthritis Receiving Background Methotrexate
NCT00282308 ·Status: COMPLETED ·Phase: PHASE2
-
The Safety and Efficacy of TLL-018 in Active Rheumatoid Arthritis
NCT05133297 ·Status: COMPLETED ·Phase: PHASE2
-
An Observational Study of MabThera (Rituximab) in Patients With Rheumatoid Arthritis And Inadequate Response Or Intolerance to a First Anti-TNF Alpha Therapy
NCT01592292 ·Status: COMPLETED
-
Optimal Management of Rheumatoid Arthritis Patients Requiring Biologic Therapy
NCT01021735 ·Status: COMPLETED ·Phase: PHASE4
-
An Observational Study of MabThera/Rituxan (Rituximab) and Alternative TNF-Inhibitors in Patients With Rheumatoid Arthritis and an Inadequate Response to a Single Previous TNF-Inhibitor
NCT01557348 ·Status: COMPLETED
-
Patients With Rheumatoid Arthritis (RA) Treated With Rituximab in Kuopio University Hospital
NCT00854321 ·Status: COMPLETED
-
A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid Arthritis on a Stable Dose of Conventional Synthetic Disease-Modifying Antirheumatic Drugs (csDMARDs) Who Have an Inadequate Response to csDMARDs Alone
NCT02675426 ·Status: COMPLETED ·Phase: PHASE3
-
Observational Safety Study of Rituximab in Patients Diagnosed With Rheumatoid Arthritis (RA) Who Did Not Respond Adequately to TNF-alpha Blocker
NCT02322801 ·Status: COMPLETED
-
Low Dose Rituximab as a First Line Biologic Therapy for the Treatment of DMARD Resistant Patients With Rheumatoid Arthritis
NCT01593332 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of Retreatment With Rituximab in Patients With Rheumatoid Arthritis Receiving Background Methotrexate
NCT00266227 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of the Safety and Efficacy of Golimumab (CNTO 148) in Subjects With Active Rheumatoid Arthritis Previously Treated With Biologic Anti-TNFa Agent(s)
NCT00299546 ·Status: COMPLETED ·Phase: PHASE3
-
A New Mode of Action of Anti-TNF, Reverse Signaling, in Rheumatoid Arthritis
NCT03216928 ·Status: COMPLETED ·Phase: NA
-
Induction and Tapering Therapy With Tofacitinib and Glucocorticoid in Patients With Polymyalgia Rheumatica
NCT06172361 ·Status: RECRUITING ·Phase: PHASE3