RecruitingPHASE1, PHASE2NCT07181837

A Phase 1/2 Study of the Safety and Efficacy of MVX-220 in Angelman Syndrome

Studying Angelman syndrome due to a point mutation

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Key facts

Sponsor
MavriX Bio, LLC
Intervention
MVX-220(genetic)
Enrollment
12 enrolled
Eligibility
4-50 years · All sexes
Timeline
20252031

Study locations (3)

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 NCT07181837 on ClinicalTrials.gov

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