Muscular Dystrophy Trial, Recruiting (NCT07138963)

Muscular Dystrophy Trial, Recruiting NCT07138963 Sponsor: Ain Shams University Condition: Muscular Dystrophy

Printed from Voxsanity (voxsanity.com.au) — NCT07138963 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.

Back to Muscular Dystrophy

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 have been diagnosed with a congenital myopathy (a muscle condition present from birth) or a congenital muscular dystrophy (an inherited muscle-weakening condition present from birth)
You are under 18 years of age
Both boys and girls can take part
Your muscle condition has been confirmed through genetic testing

Who may not be able to join:

You are 18 years of age or older
You have been diagnosed with spinal muscular atrophy (SMA) or a nerve root condition
You have a condition called congenital myasthenic syndrome, which affects how nerves and muscles communicate
You have been diagnosed with Duchenne Muscular Dystrophy (DMD), a dystrophin-related muscle condition, or Limb-Girdle Muscular Dystrophy (LGMD)
You have a muscle condition caused by a problem with the body's metabolism (how it processes energy)
You have a muscle condition caused by inflammation (where the immune system attacks the muscles)

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 28 July 2026

This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 00201092289982

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.

Voxsanity

Clinical trials and treatments, explained plainly · voxsanity.com.au

Date:

To: My Doctor

Re: Clinical trial enquiry

I am writing to enquire about the following clinical trial which may be relevant to my care:

Trial: NCT07138963

Sponsor: Ain Shams University

Phase: Not Applicable

Status: Recruiting

Condition: Muscular Dystrophy

Trial contact: 00201092289982

More information: https://clinicaltrials.gov/study/NCT07138963

Eligibility summary (AI generated)

Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

You have been diagnosed with a congenital myopathy (a muscle condition present from birth) or a congenital muscular dystrophy (an inherited muscle-weakening condition present from birth)
You are under 18 years of age
Both boys and girls can take part
Your muscle condition has been confirmed through genetic testing

Who may not be able to join:

You are 18 years of age or older
You have been diagnosed with spinal muscular atrophy (SMA) or a nerve root condition
You have a condition called congenital myasthenic syndrome, which affects how nerves and muscles communicate
You have been diagnosed with Duchenne Muscular Dystrophy (DMD), a dystrophin-related muscle condition, or Limb-Girdle Muscular Dystrophy (LGMD)
You have a muscle condition caused by a problem with the body's metabolism (how it processes energy)
You have a muscle condition caused by inflammation (where the immune system attacks the muscles)

Important: Always verify eligibility with the trial site directly before applying.

Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.

This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 28 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.

Trial details

Status

Recruiting

Phase

Not Applicable

Sponsor

Ain Shams University

Registry

ClinicalTrials.gov

Start date

30 June 2024

Est. completion

30 June 2026

Where this trial is recruiting

🇪🇬 Egypt

Primary endpoints

Phenotype and genotype of congenital myopathies (CM) and congenital muscular dystrophies (CMD) patients

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: 28 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