RecruitingPhase 2NCT07157254

A Safety and Efficacy Study of GTX-102 in Subjects With Deletion- or Nondeletion-type Angelman Syndrome (AS)

Studying Angelman syndrome due to a point mutation

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Key facts

Sponsor
Ultragenyx Pharmaceutical Inc
Principal Investigator
Medical Director
Ultragenyx Pharmaceutical Inc
Intervention
No intervention(other)
Enrollment
60 enrolled
Eligibility
1-64 years · All sexes
Timeline
20252030

Study locations (22)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07157254 on ClinicalTrials.gov

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