Cure JM Funded & Partner Clinical Trials

Cure JM is dedicated to funding and collaborating on the most promising juvenile myositis research clinical trials to shape a future free of JM. We are dedicated to supporting better treatment options through the clinical trial process to improve the lives of generations of JM patients.

CAR-T Myositis Clinical Trial

We are supporting clinical trials for promising innovative new treatments like CAR-T, a potential “immune system reset” for juvenile myositis. Early data shows promise for this therapy in cancer and autoimmune diseases like JM.

Cure JM partner Cabaletta Bio has recently opened up an adult CAR-T myositis trial for myositis patients over 18 years old, with an expected adolescent trial in the coming month, so check back regularly for updates. Learn more about this clinical trial and Cabaletta Bio’s early promising results at https://www.curejm.org/car-ttherapypotential/

JAK Inhibitor Clinical Trial – Deucravacitinib

In 2017, we partnered on a project with the NIH to screen thousands of U.S.-registered drugs to uncover compounds and drugs that are the strongest candidates for best treating juvenile myositis with fewer side effects.

Dr. Travis Kinder and the drug discovery team the NIH team.

The outcome of this screening identified several JAK inhibitors, with a drug named deucravacitinib (Sotyktu), a promising candidate to be safe and effective in treating JM, with the hope of reducing reliance on steroids and chemo treatments. Deucravacitinib shows promise in JM with a low side effect profile.

Cure JM’s research partners at the NIH will open enrollment by early 2025. The trial will begin with patients aged 18 and older, and we expect adolescents to be added to it in 2025.

Vamorolone – A Potential Steroid Alternative

We are funding pre-trial work on vamorolone with key researchers at Cure JM’s Center of Excellence at Duke University to advance a clinical trial plan with the FDA. Vamorolone is a new steroid alternative that was recently approved by the FDA for treating Duchenne Muscular Dystrophy. Vamorolone shows promise in providing the powerful benefits of corticosteroids without the harsh side effects that are often associated with prednisone.

Cure JM is working closely with Duke University, the FDA, and the distributors of vamorolone on a clinical trial plan to test safety and efficacy of the drug in JM.

Community Advisory Board

Cure JM’s Community Advisory Board plays a vital role in representing JM families from diverse backgrounds to help support this cutting edge research project. Cure JM CAB members are the link between the greater JM community and the project’s research team, working together to ensure that the needs of the entire JM community are understood and addressed.

Cadence’s Story

Cadence was only 18 months old when she was diagnosed with juvenile dermatomyositis. Her mother took her to their pediatrician’s office multiple times, only for

Balancing Work and Caregiving: Strategies for Working Parents of Children with Juvenile Myositis

Balancing Work and Caregiving: Strategies for Working Parents of Children with Juvenile Myositis

Balancing the demands of a career with the responsibilities of caregiving is a challenging task for any parent. For those with a child diagnosed with juvenile myositis (JM), a rare autoimmune disease affecting children, the challenge is heightened. Juggling work commitments while providing the necessary care and support for a child with JM can be taxing. In this article, we hope to provide you with a few effective strategies and insights to help working parents navigate this delicate balance.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

Cure JM supports families, patients, and the juvenile myositis research community.

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