Phase 2 Muscular Dystrophy Trial, By Invitation NCT06867107 Sponsor: Satellos Bioscience, Inc. Condition: Muscular Dystrophy
Back to Muscular Dystrophy

Phase 2 Muscular Dystrophy Trial, By Invitation

NCT06867107
By Invitation Phase 2 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Australian sites

The Royal Children's Hospital, Melbourne, Victoria
St. Vincent Hospital, Melbourne, Victoria

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

Status
By Invitation
Phase
Phase 2
Sponsor
Satellos Bioscience, Inc.
Registry
ClinicalTrials.gov
Start date
20 August 2025
Est. completion
30 August 2026

Where this trial is recruiting

🇦🇺 Australia

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov