CompletedNCT05783791
Development of a Newborn Screening Assay for Angelman Syndrome and Prader-Willi Syndrome
Studying Angelman syndrome due to a point mutation
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Wisconsin, Madison
- Principal Investigator
- Mei W Baker, M.D., FACMGUniversity of Wisconsin, Madison
- Intervention
- Newborn Screening Assay(diagnostic_test)
- Enrollment
- 11 enrolled
- Eligibility
- All sexes
- Timeline
- 2023 – 2023
Study locations (1)
- University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States
Collaborators
Ultragenyx Pharmaceutical Inc
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 NCT05783791 on ClinicalTrials.govOther trials for Angelman syndrome due to a point mutation
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- RECRUITINGPHASE2NCT07157254A Safety and Efficacy Study of GTX-102 in Subjects With Deletion- or Nondeletion-type Angelman Syndrome (AS)Ultragenyx Pharmaceutical Inc
- RECRUITINGNCT06737718Use of Eye Tracking to Study Social Perception Abnormalities in Children With Angelman SyndromeAssistance Publique - Hôpitaux de Paris
- ACTIVE NOT RECRUITINGPHASE3NCT06617429Phase 3 Efficacy and Safety Study of GTX-102 in Pediatric Subjects With Angelman Syndrome (AS)Ultragenyx Pharmaceutical Inc
- ENROLLING BY INVITATIONPHASE3NCT06415344Long-term Extension of GTX-102 in Angelman SyndromeUltragenyx Pharmaceutical Inc
- RECRUITINGPHASE1, PHASE2NCT05127226HALOS: A Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of Multiple Ascending Doses of ION582 in Participants With Angelman SyndromeIonis Pharmaceuticals, Inc.
- RECRUITINGNCT06229769Natural History Study for Patients With Angelman SyndromeCentre Hospitalier Universitaire de Liege
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