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Tests treatment safety and results for Idiopathic Inflammatory Myositis (IIM)
Official title Safety and Efficacy of ULSC on Disease Severity and Steroid Tapering in Participants With Dermatomyositis/ Polymyositis (DM/PM), Also Known as Idiopathic Inflammatory Myopathy (IIM)
ClinicalTrials.gov ID: NCT07160205
What this study is testing
What is ULSC (1.5 x 10^8 cells/dose)?
ULSC (1.5 x 10^8 cells/dose) is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for idiopathic inflammatory myositis (iim).
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- The goal of this clinical trial is to learn about how an umbilical cord lining-derived stem cell (ULSC) product performs when treating Dermatomyositis/Polymyositis (DM/PM), also known as idiopathic inflammatory myopathy (IIM) in adults. It will assess safety and efficacy in relieving symptoms of DM/PM with ULSC administered in three intravenous (IV) doses of 150 million cells per dose.
- Phase 3: a large, late-stage study
- You might receive a placebo (an inactive treatment) instead of the study drug.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Participants will be ≥18 years old.
- Diagnosis of idiopathic inflammatory myositis (IIM) based on 2017 EULAR/ACR Classification Criteria for adult IIM, corresponding to a score of ≥ 5.5...
- Active disease as defined by any one of the following test results:
- Elevated Creatine Kinase (CK) or Aldolase (more than 1.5 x the upper limit of normal) at screening, OR
- MRI positive for active, muscle inflammation within 12 weeks prior to screening, OR
You likely can't join if
- Adequate pulmonary function, defined as saturated oxygen (SpO2 ≥ 94%) on room air.
- Left ventricular ejection fraction (LVEF) ≥ 30% as assessed by echocardiogram (ECHO) or multigated acquisition (MUGA) scan performed within 8 weeks...
- Participants must have the ability to comply with the requirements of the study.
- All participants of reproductive age/capacity will be required to use adequate contraception, defined as at least one form of a highly effective...
- Participant will have the ability to understand and provide written informed consent. Exclusion Criteria: The presence of any of the following...
- A diagnosis of inclusion body myositis, juvenile DM or PM, myositis in the context of significant autoimmune rheumatologic disease.
See the full eligibility criteria
Who can join
- Participants will be ≥18 years old.
- Diagnosis of idiopathic inflammatory myositis (IIM) based on 2017 EULAR/ACR Classification Criteria for adult IIM, corresponding to a score of ≥ 5.5 (≥ 6.7 with muscle biopsy).
- Active disease as defined by any one of the following test results:
- Elevated Creatine Kinase (CK) or Aldolase (more than 1.5 x the upper limit of normal) at screening, OR
- MRI positive for active, muscle inflammation within 12 weeks prior to screening, OR
- EMG read as active myositis within 12 weeks prior to screening, OR
- muscle biopsy obtained within 12 weeks of the screening showing active inflammatory disease.
- Muscle weakness or active cutaneous manifestations of dermatomyositis assessed at Screening and documented with either of the following scores:
- Bilateral MMT-8 score of ≤142/150, OR
- CDASI Total Activity score of ≥ 7.
- Participants must be receiving standard of care treatment with one or more immunosuppressants or at least 5 mg prednisone (or corticosteroid equivalent).
- Immunosuppressive doses should be stable for at least 12 weeks prior to enrollment. Participants must remain on stable immunosuppressive therapy for the duration of the trial unless discontinuation is warranted due to...
- Hydroxychloroquine (HCQ) doses should be stable for at least 12 weeks prior to enrollment.
- Steroid doses should be stable for at least 4 weeks prior to enrollment. At screening and enrollment, maximum dose allowed is 25 mg/day prednisone (or corticosteroid equivalent).
- Allowed immunosuppressants include: methotrexate, azathioprine, mycophenolate, cyclosporine, IVIG, and others to be evaluated at the discretion of the investigator.
- Participants will either be:
- positive for a myositis-associated antibody, OR
- will have undergone evaluation to exclude mimics, as deemed appropriate by the Investigator. Note: The minimum workup to be performed on all prospective participants to exclude mimics is as standardly followed, which...
- Medical history and physical exam to determine the clinical course and progression of symptoms, the distribution of weakness, and the absence of features of myelopathy, neuropathy, neuromuscular disease, myotonic...
- Elevated Creatine Kinase (CK) or Aldolase levels in blood;
- Electromyography (EMG) and/or MRI of clinically affected 99+proximal muscle group;
- Myositis-specific and myositis-associated autoantibodies in blood;
- Muscle biopsy with characteristic features of IIM and excluding features of muscular dystrophy, metabolic myopathies, drug-induce myopathy, inclusion body myopathy, and necrotizing myopathy;
- Blood tests for exclusion of HIV, Hepatitis B (HBV), and Hepatitis C (HCV). [Screening tests are done for HIV ELISA, HBs Ag, HBc Ab, and HCV Ab with reflex for HCV RNA (PCR) for
What rules you out
- Adequate pulmonary function, defined as saturated oxygen (SpO2 ≥ 94%) on room air.
- Left ventricular ejection fraction (LVEF) ≥ 30% as assessed by echocardiogram (ECHO) or multigated acquisition (MUGA) scan performed within 8 weeks prior to Screening.
- Participants must have the ability to comply with the requirements of the study.
- All participants of reproductive age/capacity will be required to use adequate contraception, defined as at least one form of a highly effective contraceptive (i.e., condoms, hormonal birth control, IUD), with any...
- Participant will have the ability to understand and provide written informed consent. Exclusion Criteria: The presence of any of the following criteria excludes a participant from study enrollment:
- A diagnosis of inclusion body myositis, juvenile DM or PM, myositis in the context of significant autoimmune rheumatologic disease.
- Diagnosis of IIM as part of an overlap syndrome (except overlap with Sjogren's syndrome).
- Initiation of Rituxan (rituximab) treatment within 12 weeks of randomization. If participant is already on Rituxan, they must remain on a stable dose throughout the trial.
- Use of other biologic or investigational drug within 6 half-lives for the agent.
- Diagnosis of myositis-associated interstitial lung disease or cardiac involvement sufficient to limit participation in the trial in the discretion of the PI.
- End-stage IIM with irreversible muscle involvement seen on biopsy.
- Patients with predominant muscle atrophy secondary to uncontrolled or chronic DM or PM, based on clinical, biochemical, and/or radiologic assessment, despite previous optimized treatment.
- Non-immune myopathies.
- Cancer associated with myositis.
- Hypersensitivity to study product components including history of hypersensitivity to dimethyl sulfoxide (DMSO).
- Pregnant or lactating participants.
- Concomitant severe cardiac, pulmonary disease, active infection, or other conditions that preclude assessment of safety and how well it works of the study product.
- Anticipated need for surgery during the trial period.
- A history of prevalent noncompliance with medical therapy.
- Recipient of an organ transplant.
- Neutropenia [absolute neutrophil count \<1,800/mm\^3 (or \<1,000/mm\^3 in African-American participants)].
- Severe impairment in renal function (estimated glomerular filtration rate \<30 ml/kg\ min).
- Recent or planned use of vaccination with live attenuated viruses.
- Active cancer or prior diagnosis of cancer within the past 2 years, except non-melanoma skin cancer and carcinoma in situ of cervix Potential participants diagnosed with IIM \<3 years before screening will have...
- Participants with current or prior hepatitis B infection that could be at risk for reactivation. [For eligibility, screening test results must be HBsAg (DNA) negative and anti-HBc (core antibody total) negative).]
- Participant with HIV or active Hepatitis C. [For eligibility, the following screening tests must have negative or non-reactive results: HIV ELISA, HCV Ab with reflex for HCV RNA (PCR); if HCV Ab test is positive...
- Condition that would impair an assessment of muscle strength, including neurological disorders such as Parkinson's disease or severe musculoskeletal condition.
- Any other condition that, in the judgment of the Investigator or Sponsor, would be a contraindication to enrollment, study product administration, or follow-up.
The study team makes the final eligibility decision.
Where it's taking place
- Gainesville, Florida, United States
- Miami, Florida, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Gainesville, Florida, United States; Miami, Florida, United States. Enter your location above to see the nearest site and check your eligibility.
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BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.