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.

Parrish Story of Hope

Parrish’s Story

We would like to introduce a one-of-a-kind, competitive, and determined young man, named Parrish. His story of resiliency and hope is one that will resonate with many of us in the Cure JM family. Parrish faced many challenges in his journey with JM, but found hope and support in his family and the Cure JM community. We are pleased to now share his experience to help others facing the same struggles during Myositis Awareness Month.

2025 Family Conference Image

2025 Cure JM Family Conference

We are excited to announce that the Cure JM National Family Conference will be back in 2025! Join us for three days with world-class JM researchers, engaging sessions for all, and social time to connect with new friends. The 15th Annual Cure JM National Family Conference is taking place June 27th -June 29th, 2023, in Chicago, Illinois.

Volunteering Speaks Volumes

Are you eager to make a meaningful impact and connect with a community committed to an important cause? The Cure JM Foundation welcomes passionate volunteers like you! Whether you can spare just a few moments or have more time to give, your dedication can greatly advance our mission.

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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