RecruitingPhase 2NCT06508931
Safety and Efficacy Study of Zamtocabtagene Autoleucel (MB-CART2019.1) in Pediatric Patients With R/R B-Cell Neoplasms
Studying B-cell non-Hodgkin lymphoma
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
- Miltenyi Biomedicine GmbH
- Principal Investigator
- Birgit Burkhardt, Prof. Dr.Uniklinik Münster, Klinik für Kinder- und Jugendmedizin Pädiatrische Hämatologie/Onkologie
- Intervention
- zamtocabtagene autoleucel (MB-CART2019.1)(drug)
- Enrollment
- 31 target
- Eligibility
- 17 years · All sexes
- Timeline
- 2025 – 2029
Study locations (1)
- Institut Gustave Roussy, Villejuif, France
Collaborators
PPD, Part of Thermo Fisher Scientific
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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