Phase 2 Muscular Dystrophy Trial, By Invitation
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You must have already taken part in the related "parent" clinical trial called SAT-3247-CL-101.
- Your steroid medication dose (if you take one) must have stayed the same since the parent trial, or you must not be taking steroids at all.
- Any other regular medicines, supplements, or over-the-counter products you take must have stayed at the same doses since the parent trial.
- You must be able to understand what the trial involves and any risks that come with taking part.
- You must be able to communicate clearly with the trial team and follow all trial requirements, including attending visits, doing tests, filling in questionnaires, and wearing any devices provided.
- You (and a parent or legal guardian if needed) must be willing to sign a consent form after being fully informed about the trial.
- If you are sexually active, you must agree to follow the birth control and sperm donation rules set out in the trial plan.
Who may not be able to join:
- You have a serious current or ongoing health condition (other than Duchenne Muscular Dystrophy) that could make participation unsafe or affect the results.
- You are expected to need spine surgery or a planned hospital stay for a non-emergency health reason within the next 12 months.
- You currently have stomach or gut symptoms (such as nausea, vomiting, diarrhoea, or heartburn), an active infection (such as flu), or a significant infection or inflammation at the time of your screening appointment.
- You have serious behavioural or thinking difficulties that would prevent you from taking part, in the opinion of the trial doctor.
- You have developed heart muscle problems with symptoms since finishing the parent trial.
- You are unable to swallow tablets (though tablets may be split or crushed and mixed into food or a flavoured drink, so confirm with the trial site if this applies to you).
- You have taken part in another clinical trial or received another experimental treatment since finishing the parent trial (confirm with trial site if you have used deflazacort or vamorolone, as these may be exceptions depending on your location).
- The trial team believes you may not be able or willing to follow the trial requirements.
- You are an employee, contractor, or consultant of the company running the trial, the research organisation supporting it, or the trial site — or you are a close relative of someone who is.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Australian sites
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
2 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Treatment emergent adverse events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.