TerminatedPhase 1NCT03203369
Study to Evaluate the Safety and Clinical Activity of UCART123 in Patients With BPDCN
Studying Blastic plasmacytoid dendritic cell neoplasm
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
- Cellectis S.A.
- Principal Investigator
- Ioana Kloos, MD, M.DCellectis S.A.
- Intervention
- UCART123(biological)
- Enrollment
- 1 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2017 – 2019
Study locations (1)
- MD Anderson Cancer Center, Houston, Texas, United States
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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