RecruitingNCT06941025
Maternal and Postnatal Outcomes Study (MOS): A Global Observational Registry Assessing the Safety of Elfabrio® in Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding
Studying Fabry disease
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
- Chiesi Farmaceutici S.p.A.
- Intervention
- Not applicable- observational study(other)
- Enrollment
- 10 enrolled
- Eligibility
- FEMALE
- Timeline
- 2025 – 2034
Study locations (5)
- No physical study sites - Decentralized, web-based registry, Washington D.C., District of Columbia, United States
- No physical study sites - Decentralized, web-based registry, Berlin, Germany
- No physical study sites - Decentralized, web-based registry, Rome, Italy
- No physical study sites - Decentralized, web-based registry, Madrid, Spain
- No physical study sites - Decentralized, web-based registry, London, United Kingdom
Collaborators
ICON plc
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.
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