Not yet recruitingPHASE1, PHASE2NCT06736080
Safety and Efficacy of Gene Therapy of FHL Type 3 Caused by Mutations in the Human UNC13D Gene by Transplantation of a Single Dose of Autologous CD34+ Cells Transduced Ex Vivo with the UNC13D LV Vector Expressing the UNC13D CDNA
Studying Acquired hemophagocytic lymphohistiocytosis associated with malignant 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
- Assistance Publique - Hôpitaux de Paris
- Principal Investigator
- Jean-Sébastien DIANA, MD, PhDAssitance publique - Hôpitaux de Paris
- Intervention
- MUNC-CD34(drug)
- Enrollment
- 5 enrolled
- Eligibility
- 17 years · All sexes
- Timeline
- 2025 – 2029
Study locations (1)
- Hôpital Necker Enfant Malades, Paris, France
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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