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Arthritis, Rheumatoid clinical trials

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NCT ID: NCT02633332 Completed - Clinical trials for Rheumatoid Arthritis

Use of Well Known Drugs for New Destination - RA Improvement (RANT)

RANT
Start date: February 2015
Phase: Phase 1
Study type: Interventional

The purpose of this interventional study is to determine whether tetracyclines, statins, antiviral and Vitamin D3 in single subministration are effective in improvement of life and health condition in the treatment of rheumatoid arthritis due to autoimmune disease (RA) in all his forms, specially in patients intolerant to commonly used treatments.

NCT ID: NCT02632890 Completed - Clinical trials for Rheumatoid Arthritis

Assessment of the Effectiveness of IV and SC Abatacept (Orencia) Patient Alert Cards in Patients With Rheumatoid Arthritis in a Sample of EU Countries

Start date: November 29, 2016
Phase: N/A
Study type: Observational

The purpose of the study is to determine a) if the implementation of abatacept (Orencia®) patient alert card (PAC) resulted in effective understanding of key safety messages and b) if the degree of understanding of key safety messages is associated with improved clinical and safety outcomes.

NCT ID: NCT02627924 Completed - Clinical trials for Rheumatoid Arthritis

Real-World Outcome of Rheumatoid Arthritis Patients in Korea on Adalimumab

ROCKA
Start date: November 18, 2015
Phase:
Study type: Observational

The study is designed as a prospective, observational study to assess the effect of adalimumab on health-related quality of life (QoL) and work productivity in patients with rheumatoid arthritis (RA) in Korea.

NCT ID: NCT02626026 Completed - Clinical trials for Rheumatoid Arthritis

Study to Evaluate Safety and Pharmacokinetics of GS-4059 (Tirabrutinib) in Healthy Volunteers and Participants With Rheumatoid Arthritis (RA)

Start date: January 26, 2016
Phase: Phase 1
Study type: Interventional

This study will consist of two parts: Part A will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of tirabrutinib in healthy participants. Part B will evaluate the safety, tolerability, and the effect of tirabrutinib on disease-specific clinical markers and outcomes in participants with rheumatoid arthritis (RA).

NCT ID: NCT02622503 Completed - Clinical trials for Rheumatoid Arthritis

A Study on Rheumatoid Arthritis Patients Treated With Rituximab

Start date: April 2008
Phase: N/A
Study type: Observational

The purpose of the study is to obtain an overall picture of rituximab treatments and treatment responses in RA patients.

NCT ID: NCT02620189 Completed - Clinical trials for Rheumatoid Arthritis

Th17 Responses Evaluated in RA Patients on Inhibitors of TNFα

THERAPIST
Start date: March 2015
Phase:
Study type: Observational

Preliminary data suggest that up-regulation of Interleukin -17 (IL-17) and the T-helper 17 (Th17) pathway occurs in rheumatoid arthritis (RA) patients on anti-Tumour Necrosis Factor (TNF) therapy who demonstrated an incomplete clinical response. A deeper understanding of this is required in order to determine whether IL-17 or the Th17 pathway is a valid target for intervention in this population to improve response outcome. The study objective is to observe biologic naïve RA subjects on anti-TNF therapies and take measurements of peripheral blood and synovial tissue to assess differences in the IL-17 and Th17 pathways between responders and non-responders. The aim of the study is to test if increased Th17 pathway activity is present in subjects who do not respond clinically to anti-TNF therapy. Clinical assessments, synovial bio-markers and ultrasound will be used as determinants of clinical response. The study may identify disease characteristics that determine which subjects may be more likely to respond to anti-TNF therapy, or those who may require either a different treatment option, or additional pathway inhibition in addition to TNF, in order to achieve clinical response.

NCT ID: NCT02618954 Completed - Clinical trials for Rheumatoid Arthritis in Remission

Role of Ultrasound for Evaluating Rheumatoid Arthritis in Remission

SONORE
Start date: September 2013
Phase: N/A
Study type: Interventional

The objective of this study is to determine the longitudinal relation between clinical remission and ultrasound (US) remission in Rheumatoid arthritis (RA). At a patient level, US-detected residual synovitis (evaluated both by US grey-scale signals and power Doppler signals) is frequent in patients with RA in clinical remission. Several longitudinal studies reveal an association of US-detected residual synovitis and risk of relapse and radiographic progression, in individual patients and joints, over 1-2 years. However, the longitudinal relation between clinical remission and US remission is not so well-known and it is possible that clinical remission arrive before ultrasound remission. Thus arise the question as to whether the presence of US-detected residual synovitis require to adapt the treatment to ultrasound findings or to simply increase the patient care. The investigator propose to conduct a prospective, bi-center, non randomized study.

NCT ID: NCT02616380 Completed - Clinical trials for Rheumatoid Arthritis

Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in Taiwan

ROCKI
Start date: November 5, 2015
Phase:
Study type: Observational

The study is designed as a prospective, observational study to assess the effect of adalimumab on health-related quality of life (QoL) and work productivity in patients with rheumatoid arthritis (RA) in Taiwan.

NCT ID: NCT02615951 Completed - Healthy Volunteers Clinical Trials

Characterization of Breg Cells

Breg
Start date: October 2, 2015
Phase: N/A
Study type: Interventional

Recently, it has been shown that B cells could also have regulatory functions through the secretion of interleukin 10 (IL-10). They are called the B regulatory cells (Breg). In the mouse model the most commonly used of rheumatoid arthritis, collagen-induced arthritis (CIA), the transfer Breg helps prevent the development of CIA and cure established arthritis. The investigators have recently shown that Breg were decreased in patients with RA compared to controls and that the rate of Breg was inversely correlated with disease activity and autoantibody. These results thus suggest that the lack of IL-10 secretion by B cells plays an important role in the pathophysiology of RA. Nevertheless, in humans, the Breg remain poorly understood. The main objective of this project is to better characterize the B capable of producing IL-10 both in subjects with RA and controls. Understanding which induces the secretion of IL-10 by B could allow to consider new therapeutic approaches in autoimmune diseases, including in RA. The investigators therefore aim to identify nutrient transporters, chemokine receptors, genes and surface proteins differentially expressed between Breg and other B cells in patients with RA and in controls.

NCT ID: NCT02608112 Completed - Clinical trials for Rheumatoid Arthritis

Study to Describe Real World Drug Retention Rate of the Tocilizumab at One Year

Start date: December 31, 2015
Phase:
Study type: Observational

This multicenter, prospective, non-interventional study is designed to obtain an accurate estimation of the drug retention rate of Tocilizumab (TCZ) Subcutaneously (SC) under real-world conditions in participants with moderate to severe rheumatoid arthritis (RA).