Oculopharyngeal Muscular Dystrophy

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Review clinical trials related to Oculopharyngeal Muscular Dystrophy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Oral Health, Saliva Viscosity and Composition in Oculo-Pharyngeal Muscular Dystrophy (OPMD)

The goal of this observational study is to explore whether oral health and saliva viscosity and composition in Oculopharyngeal Muscular Dystrophy (OPMD) is different from control subjects. The main questions it aims to answer are: Do swallowing disturbances in OPMD adversely affect oral health? Is saliva thickness (viscosity) is increased in OPMD? Does saliva in OPMD contains biochemical markers of the disease?

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sheba Medical CenterUpdated: Jan 27, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Patients with OPMD and their spouses or household members

• Pregnancy or presence of any disease that may affect a composition of saliva

Status: Recruiting

A Study to Evaluate the Safety and Clinical Activity of Intramuscular Doses of BB-301 Administered to Subjects With Oculopharyngeal Muscular Dystrophy With Dysphagia

Subjects who have enrolled in the oculopharyngeal muscular dystrophy (OPMD) natural history study (Study BNTC-OPMD-NH-001) and have completed at least 6 months of follow up in Study BNTC-OPMD-NH-001 may be eligible to participate in this study, where all subjects will be treated with a single dose of BB-301. BB-301 will be injected directly into the middle pharyngeal constrictor muscle and the inferior pharyngeal constrictor muscle of the throat through the use of an open surgical procedure conducted under general anesthesia. The primary objectives of the study are to evaluate the safety of BB-301, to identify the best dose of BB-301 to administer to patients, and to characterize how well BB-301 works to improve the symptoms of dysphagia in patients with OPMD.

Participants needed: 30
Trial details
Phase: Phase 1, Phase 2Age: Up to 65Biological sex: AllType: InterventionalSponsor: Benitec Biopharma, Inc.Updated: Dec 31, 2025Locations: 1
Eligibility criteria

Subject was previously enrolled in the BNTC-OPMD-NH-001 natural history (NH) stu... [+11]

Subject has received prior treatment with an adeno-associated virus (AAV) vector... [+26]