RecruitingNot applicableNCT05805202
Functional Implications of Rare Gene Mutations in aHUS Open the Door to Personalized Therapy
Studying Atypical hemolytic uremic syndrome
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
- Mario Negri Institute for Pharmacological Research
- Intervention
- Blood sampling and urine analysis(other)
- Enrollment
- 112 enrolled
- Eligibility
- All sexes
- Timeline
- 2023 – 2026
Study locations (1)
- Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò", Ranica, BG, Italy
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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