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Taking people in GermanyPhase 1/2

Long-term follow-up of people treated with Miltenyi CAR T cell therapies

Follows people with blood cancers treated with modified immune cells over time.

Plain-language title generated from the registry record
Registry title: Long-Term Follow-up of Patients Treated With Miltenyi Cell and Gene Therapies

Key facts

Where
Berlin, Cologne, Erlangen, Goettingen, Muenster, Munich, Tuebingen, and Wuerzburg, GermanySee the 9 sites
Phase
Phase 1/2

Where in Germany

  • Charite Universitaetsmedizin Berlin KöRBerlin, GermanyTaking people
  • University Hospital Cologne AöRCologne, GermanyTaking people
  • Universitaetsklinikum Erlangen AöRErlangen, GermanyTaking people
  • Universitaetsmedizin GoettingenGoettingen, GermanyTaking people
  • Universitaetsklinikum Muenster AöRMuenster, GermanyTaking people
  • Westfaelische Wilhelms-Universitaet MuensterMuenster, GermanyTaking people
  • Klinikum der Universitaet Muenchen AöRMunich, GermanyTaking people
  • Universitaetsklinikum Tuebingen AöRTuebingen, GermanyTaking people
  • Universitaetsklinikum Wuerzburg AöRWuerzburg, GermanyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Miltenyi Biomedicine GmbH
Trial code
NCT06508775EU 2022-501648-14-00
Record updated
9 October 2026
Original description
The goal of this Long-Term Follow-Up Trial is to assess long-term safety and efficacy of Miltenyi CAR T treatment.Read full original descriptionShow less

Long-Term Follow-up of Patients Treated With Miltenyi Cell and Gene Therapies

The goal of this Long-Term Follow-Up Trial is to assess long-term safety and efficacy of Miltenyi CAR T treatment.

Inclusion: Patient underwent treatment with a Miltenyi CAR T cell therapy in one of the parent trials at least 12 months prior to enrollment in long-term follow-up; Patient has provided informed consent prior to enrollment.

Exclusion: No exclusion criteria.

ClinicalTrials.gov NCT06508775 · EU CTIS 2022-501648-14-00