Clinical Trials Logo

Myositis, Inclusion Body clinical trials

View clinical trials related to Myositis, Inclusion Body.

Filter by:
  • Active, not recruiting  
  • Page 1

NCT ID: NCT05721573 Active, not recruiting - Clinical trials for Inclusion Body Myositis

A Study to Evaluate the Efficacy and Safety of ABC008 for Inclusion Body Myositis

Start date: February 28, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

A Phase II/III Randomized, Double-blind, Placebo-controlled, Multicenter Study to Determine the Efficacy and Safety of ABC008 in the Treatment of Subjects with Inclusion Body Myositis

NCT ID: NCT05046821 Active, not recruiting - Clinical trials for Inclusion Body Myositis

Sporadic Inclusion Body Myositis Natural History Study

INSPIRE-IBM
Start date: October 11, 2021
Phase:
Study type: Observational

This is a prospective natural history study on patients with clinically defined sIBM. Participants will be assessed every 6 months over two years (five visits total). We will include 150 participants, enrolled across 13 sites, with sporadic IBM, diagnosed according to established criteria.

NCT ID: NCT04975841 Active, not recruiting - Clinical trials for Inclusion Body Myositis

Inclusion Body Myositis Treatment With Celution Processed Adipose Derived Regenerative Cells

Start date: March 10, 2022
Phase: N/A
Study type: Interventional

This is an open-label, single arm study evaluating the safety for patients with Inclusion Body Myositis. A total of 9 subjects will be enrolled in the study. Subjects will be randomized to Part 1 or Part 2 of the study in blocks of 3 every 3 months. Stem cell injections will be given in the forearm and thigh on either the left or right side of the body, depending on which side meets criteria. The overall goal of this pilot study is to test the safety of adipose derived regenerative cells in patients with Inclusion Body Myositis. If determined safe, this trial could lead to larger Phase II trials. While this specific trial's primary endpoint is safety, it our ultimate hope that ADRC injections into the forearm and thigh of IBM patients will slow, stabilize, or even reverse the progression of muscle weakness in patients with IBM.

NCT ID: NCT04659031 Active, not recruiting - Clinical trials for Inclusion Body Myositis

A Phase 1 Study of ABC008 in Ascending (Single Ascending Dose/Multiple Ascending Dose) Study in Patients With (IBM)

Start date: May 25, 2021
Phase: Phase 1
Study type: Interventional

An open-label, ascending dose study for adult patients with Inclusion Body Myositis (IBM).

NCT ID: NCT02483845 Active, not recruiting - Clinical trials for Inclusion Body Myositis (IBM)

Natalizumab in Inclusion Body Myositis (IBM)

IBM-NAT
Start date: May 2013
Phase: Phase 1
Study type: Interventional

Muscle biopsies of patients with Inclusion Body Myositis (IBM) have demonstrated a T-cell predominant inflammatory infiltrate, therefore, new agents targeting T -cell mediated cell death may be a novel treatment for IBM. Such an agent capable of preventing T-cell movement out of the vasculature, such as natalizumab, may be beneficial in IBM patients. Six patients will be recruited to participate in this phase I trial.

NCT ID: NCT01734369 Active, not recruiting - Dermatomyositis Clinical Trials

Environmental Risk Factors for Myositis in Military Personnel

Start date: March 13, 2014
Phase:
Study type: Observational

Background: - Myositis is a rare disease in which the body s immune cells attack the muscle tissue. It can cause muscle weakness, swelling, and pain. It can develop in people with no history of muscle problems. Environmental exposures may determine who develops myositis. Genes may also affect development of the disease. - Some people who serve in the military develop myositis. However, other military personnel do not. Researchers want to compare military personnel with and without myositis. They will look for common factors that might have led to the disease. Objectives: - To study environmental risk factors for myositis in military personnel. Eligibility: - Military personnel who developed myositis during their period of service. - Healthy military personnel who do not have myositis or another autoimmune disease. Design: - Participants will have a physical exam and medical history. - Participants will fill out forms about environmental exposures, particularly while in the military. The questions will ask about past infections, vaccines and medications, and personal habits. They will also ask about participants occupations during military service and their deployments. - Participants will also provide blood samples for study. - No treatment will be provided as part of this study.