RecruitingNCT06299748
A Worldwide Pregnancy Safety Study to Assess Maternal, Fetal, and Infant Outcomes Following Exposure to Efgartigimod During Pregnancy and/or Breastfeeding.
Studying Adult-onset myasthenia gravis
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
- argenx
- Intervention
- Efgartigimod(biological)
- Enrollment
- 279 enrolled
- Eligibility
- FEMALE
- Timeline
- 2023 – 2033
Study locations (4)
- United BioSource LLC, Morgantown, West Virginia, United States
- Klinikum der Ruhr-Universität Bochum St. Josef Hospital Neurologische Interdisziplinäre Infusionsambulanz + MS Studienambulanz (Haus E Ebene1), Bochum, Germany
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy
- Hospital Universitari Vall d'Hebron, Barcelona, Spain
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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