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Arthritis clinical trials

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NCT ID: NCT00548834 Completed - Clinical trials for Rheumatoid Arthritis

Efficacy and Safety of CDP870 Versus Placebo in the Treatment of the Signs and Symptoms of Rheumatoid Arthritis

Start date: June 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study was to confirm and extend the data from previous studies and to demonstrate the efficacy (in terms of signs and symptoms) and safety of monotherapy with CDP870 administered SC every 4 weeks compared to placebo in patients with active RA who had failed at least one DMARD.

NCT ID: NCT00547521 Completed - Clinical trials for Rheumatoid Arthritis (RA)

Phase IIIB Subcutaneous Abatacept Monotherapy Study

Start date: December 2007
Phase: Phase 3
Study type: Interventional

To evaluate safety and immunogenicity of abatacept when used with or without methotrexate in the absence of an IV loading dose of abatacept

NCT ID: NCT00546533 Completed - Clinical trials for Rheumatoid Arthritis

Study Evaluating the Efficacy and Safety of Etanercept

Start date: January 2003
Phase: Phase 4
Study type: Interventional

To assess the efficacy of etanercept 25 mg administered subcutaneously twice-weekly for 12 weeks in patients with active RA for whom classical antirheumatic therapy is insufficient or inappropriate.

NCT ID: NCT00545454 Completed - Clinical trials for Rheumatoid Arthritis

Activity and Safety of Oral Administration of SSR150106XB for the Reduction of Inflammation in Patients With Active Rheumatoid Arthritis

ACCORD-RA
Start date: October 2007
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the reduction of systemic inflammation as measured by serum levels of C-reactive protein (CRP). The secondary objectives are: - to assess the reduction of systemic inflammation as measured changes in acute phase protein, serum amyloid A (SAA) and cytokine interleukin-6 (IL-6), and clinical American College of Rheumatology response rate, and morning stiffness duration; - to assess the effect on pain relief within first 14 days; - to obtain evidence of the safety and tolerability of SSR150106; - to document trough plasma levels of SSR150106 and its first metabolite.

NCT ID: NCT00544154 Completed - Clinical trials for Arthritis, Rheumatoid

Efficacy and Safety of CDP870 and Methotrexate Compared to Methotrexate Alone in Subjects With Rheumatoid Arthritis

Start date: October 2002
Phase: Phase 3
Study type: Interventional

The main purpose of the study was to determine the efficacy of CDP870 in treating RA signs/symptoms in patients who were partial responders to MTX. Other purposes were to show additional efficacy without increased toxicity and the immunogenic response to CDP870 during combined CDP870 and MTX therapy.

NCT ID: NCT00542022 Completed - Clinical trials for Arthritis, Rheumatoid

Efficacy, Tolerability and Safety Study in Rheumatoid Arthritis (0812-008)

Start date: June 2004
Phase: Phase 2
Study type: Interventional

To demonstrate the clinical effectiveness of MK0812 in the treatment of Arthritis.

NCT ID: NCT00539760 Completed - Clinical trials for Arthritis, Rheumatoid

A Phase I Rheumatoid Arthritis Study in Healthy Volunteers

Start date: September 5, 2007
Phase: Phase 1
Study type: Interventional

GSK182771 is a domain antibody targeting the interleukin (IL)-1 receptor which is being developed for the treatment of rheumatoid arthritis. This study is being done in healthy volunteers to verify the safety and tolerability of GSK182771

NCT ID: NCT00538902 Completed - Clinical trials for Rheumatoid Arthritis

Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis Subjects Treated With Methotrexate

Start date: August 2007
Phase: Phase 2/Phase 3
Study type: Interventional

A study to assess the safety and efficacy of adalimumab administered as a subcutaneous injection in adult Chinese subjects with rheumatoid arthritis and treated with methotrexate

NCT ID: NCT00537667 Terminated - Clinical trials for Rheumatoid Arthritis

The SPECTRA Study

Start date: August 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare IL-1ra and the combination of IL-1ra and PEGsTNF-RI with respect to their ability to reduce inflammation and bone and cartilage destruction in the synovium of subjects with rheumatoid arthritis.

NCT ID: NCT00537589 Completed - Arthritis Clinical Trials

Ultrasound Guided Arthrocentesis

UGA
Start date: December 2004
Phase: N/A
Study type: Interventional

Does ultrasound guidance improve success rate and decrease aspiration attempts for peripheral arthrocentesis?