New drug aims to build muscle in rare muscular dystrophy
NCT ID NCT07435129
First seen Jun 25, 2026 · Last updated Sep 03, 2026 · Updated 5 times
Summary
This Phase 2 study tests a drug called apitegromab in 60 adults with facioscapulohumeral muscular dystrophy (FSHD), a genetic condition that causes muscle weakness. Participants will receive either the drug or a placebo every 4 weeks for a year. The main goal is to see if the drug increases total lean muscle volume, with a secondary focus on muscle function and safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- apitegromab (a lab-made antibody that blocks a protein called myostatin, which limits muscle growth)
- What this could lead to
- If it works, this could point toward a treatment that helps people with FSHD build and maintain muscle, slowing the disease's progression.
- What could go wrong
- This is an early Phase 2 trial with only 60 people, so results may not apply to everyone. The main goal is muscle volume, not yet proven to improve daily life. Side effects from the IV infusions are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female participants, 18 to 60 years of age at the time of informed consent. 2. Genetic diagnosis of FSHD Type 1 or FSHD Type 2, confirmed with the appropriate documentation from an accredited laboratory 3. Clinical severity score of 1.5 to 3.0 (Ricci score; range 0 to 5), inclusive, at screening 4. Baseline 10-meter walk/run test time ≤5 seconds Exclusion Criteria: 1. Prior history of a hypersensitivity reaction to a mAb or recombinant protein bearing an Fc domain (eg, a soluble receptor-Fc fusion protein), apitegromab, or excipients of apitegromab 2. Treatment with other investigational drugs in a clinical trial within 3 months or 5 half-lives, whichever is longer, before screening 3. Previous treatment with apitegromab, or with other anti-myostatin therapies, including activin receptor antagonists 4. Current or prior use of anabolic steroids, growth hormones, glucagon-like peptide-1 receptor agonist or other substances with known effects on muscle. 5. Use of therapies with potentially significant muscle effects (eg, androgens, insulin-like growth factor, growth hormone, systemic beta-agonist, botulinum toxin, or muscle relaxants or muscle-enhancing supplements) or potentially significant neuromuscular effects (eg, acetylcholinesterase inhibitors) within 60 days before screening 6. Use of systemic or corticosteroids within 60 days prior to screening. Inhaled or topical steroids are allowed. 7. Pregnant or breastfeeding. 8. Contraindications for MRI that may include, but are not limited to, certain implanted electronic devices, cochlear implants, metallic foreign bodies, vascular clips, and metallic implants; or claustrophobia, contrast agent allergies, inability to lie still, or external medical devices that may not be removed. 9. History of alcoholism, or illicit drug use (drugs that are illegal and have not been prescribed). 10. Taking medications that impede coagulation or platelet aggregation or has a history or active coagulopathy disorder. 11. Any acute or comorbid condition interfering with the well-being of the participant within 7 days prior to screening, including active systemic infection, the need for acute treatment, or inpatient observation due to any reason
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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National Neuromuscular Research Institute
RECRUITINGAustin, Texas, 78759, United States
More trials for these conditions
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- Personalized exercise program aims to boost mobility in rare muscle diseases
- 450 FSHD patients join Long-Term study to unlock better treatments
- New hope for FSHD: Long-Term drug safety trial underway
- New hope for FSHD: experimental drug AOC 1020 completes early testing