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Dermatomyositis clinical trials

View clinical trials related to Dermatomyositis.

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NCT ID: NCT02880527 Completed - Dermatomyositis Clinical Trials

Study of the Prevalence of Polymyositis and Dermatomyositis in Normandy

EPIDEMYOSITIS
Start date: July 2014
Phase: N/A
Study type: Observational

Polymyositis and dermatomyositis are characterized by the association to a myopathic syndrome, inflammatory infiltrates in the skeletal muscle. They remain, even today, an important factor of morbidity and mortality in these patients. At present, studies that evaluated the prevalence of polymyositis / dermatomyositis are very few; they were mainly recorded in the United States and Japan, the prevalence of polymyositis / dermatomyositis has been estimated between 3.5 and 21.5 cases / 100 000 (according to the old diagnostic criteria of Bohan and Peter). However, previous works are old and retrospective; above all, they have almost always been performed (90% of cases) from cases reported to the hospital, leading to selection bias and an underestimate of the true prevalence of polymyositis / dermatomyositis in the general population. Thus, these data lead to achieve this epidemiological study, descriptive, multicenter, based on the population of Normandy.

NCT ID: NCT02780674 Completed - Clinical trials for Dermatomyositis, Polymyositis, Sjogren's, SLE, SSc

A Phase 1 Study of MEDI7734 in Type I Interferon-Mediated Autoimmune Diseases

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

To evaluate the safety and tolerability of escalating, single subcutaneous doses of MEDI7734 in adult subjects with type I interferon-mediated autoimmune diseases.

NCT ID: NCT02728752 Completed - Dermatomyositis Clinical Trials

Study Evaluating Efficacy and Safety of Octagam 10% in Patients With Dermatomyositis (Idiopathic Inflammatory Myopathy)

IIM
Start date: February 27, 2017
Phase: Phase 3
Study type: Interventional

Prospective, Double-blind, Randomized, Placebo-Controlled Phase III Study Evaluating Efficacy and Safety of Octagam 10% in Patients With Dermatomyositis ("ProDERM study")

NCT ID: NCT02612857 Completed - Dermatomyositis Clinical Trials

Trial of IMO-8400 in Adult Patients With Dermatomyositis

8400-211
Start date: November 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine how safe and effective IMO-8400 is in adults with dermatomyositis.

NCT ID: NCT02594735 Completed - Dermatomyositis Clinical Trials

Abatacept in Juvenile Dermatomyositis

AID
Start date: November 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of subcutaneous abatacept in 10 patients seven years of age and older with refractory JDM.

NCT ID: NCT02267005 Completed - Clinical trials for Juvenile Dermatomyositis

The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis

Start date: March 2015
Phase: N/A
Study type: Interventional

This project will bring together a multidisciplinary team of pediatric rheumatologists, neurologists, metabolic geneticists and exercise physiologists to determine the effect of creatine (CR) supplementation on muscle function and muscle metabolism in children with Dermatomyositis (DM). The investigators propose using well-established exercise testing techniques as well as new, powerful exercise imaging protocols in order to better delineate the effects of CR on muscle pathophysiology in a non-invasive way. Evidence from this study will provide information regarding the effect of creatine supplementation on muscle function in DM. Improvements in muscle function and fatigue through CR use may also contribute to an improvement in quality of life and have significant clinical implications for the treatment of children with DM.

NCT ID: NCT02245841 Completed - Dermatomyositis Clinical Trials

Efficacy and Safety of H.P. Acthar Gel for the Treatment of Refractory Cutaneous Manifestations of Dermatomyositis

Start date: June 15, 2015
Phase: Phase 4
Study type: Interventional

This study will assess the safety and efficacy of H.P. Acthar gel for treating the cutaneous manifestations in patients with refractory classic dermatomyositis, juvenile dermatomyositis, and amyopathic dermatomyositis. Our hypothesis is that H.P. Acthar gel will be both safe and effective for such patients.

NCT ID: NCT02159651 Completed - Clinical trials for Interstitial Pneumonia Associated With Polymyositis/Dermatomyositis

A Survey for Long-term Use of Prograf Capsules in Patient With Interstitial Pneumonia

Start date: April 1, 2014
Phase:
Study type: Observational

This study is to evaluate the safety and the efficacy of Prograf in patients with interstitial pneumonia associated with polymyositis / dermatomyositis in acute clinical setting.

NCT ID: NCT02043548 Completed - Dermatomyositis Clinical Trials

Tocilizumab in the Treatment of Refractory Polymyositis and Dermatomyositis

TIM
Start date: October 1, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this multi-center pilot study is to determine if the drug tocilizumab (Actemra) is effective in the treatment of patients with refractory adult polymyositis (PM) and dermatomyositis (DM).

NCT ID: NCT01906372 Completed - Dermatomyositis Clinical Trials

Acthar in Treatment of Refractory Dermatomyositis and Polymyositis

Start date: September 2013
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to evaluate the effectiveness of the study drug, ACTH Gel in people diagnosed with dermatomyositis a disease that causes muscle weakness and is associated with a rash (DM) or polymyositis (PM) a disease that causes muscle weakness without a rash. The study doctors want to evaluate whether ACTH Gel will improve the symptoms of this disease. This drug is approved by the Food and Drug Administration (FDA) for dermatomyositis (DM) and polymyositis (PM). ACTH gel has been an FDA-approved treatment for myositis since 1952, and in 2010 the FDA retained PM and DM as diseases approved for ACTH gel use.