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Taking people in SpainPhase 4

Long-term safety follow-up of people treated with cilta-cel for multiple myeloma

Follows adults with multiple myeloma previously treated with cilta-cel to study late side effects.

Plain-language title generated from the registry record
Registry title: A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel

Key facts

Where
Badalona, Barcelona, Madrid, Pamplona, Salamanca, and Sevilla, SpainSee the 7 sites
Phase
Phase 4

Where in Spain

  • Institut Catala d'OncologiaBadalona, SpainTaking people
  • Hospital Clinic de BarcelonaBarcelona, SpainTaking people
  • Hospital General Universitario Gregorio MarañónMadrid, SpainTaking people
  • Hospital Universitario 12 de OctubreMadrid, SpainTaking people
  • Clínica Universidad de navarraPamplona, SpainTaking people
  • Hospital Universitario De SalamancaSalamanca, SpainTaking people
  • University Hospital Virgen Del Rocio S.L.Sevilla, SpainTaking 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
Janssen Research & Development, LLC
Trial code
NCT05201781EU 2023-505530-10-00
Record updated
3 November 2026
Original description
The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.Read full original descriptionShow less

Long-term Follow-up Study for Participants Previously Treated With Ciltacabtagene Autoleucel

The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.

Inclusion: Participants who have received at least one dose of cilta-cel in a Company-sponsored clinical study; Participants who have provided informed consent for this study.

ClinicalTrials.gov NCT05201781 · EU CTIS 2023-505530-10-00