Safety, Activity and Cell Kinetics of CYAD-211 in Patients With Relapsed or Refractory Multiple Myeloma
Condition(s) studied
Investigational drug(s) / intervention(s)
CYAD-211: Allogeneic anti-BCMA chimeric antigen receptor (CAR) T-cell
Endoxan: Preconditioning chemotherapy
Fludara: Preconditioning chemotherapy
Study summary
The purpose of the IMMUNICY-1 study is to assess the safety, activity and cell kinetics of CYAD-211 in adults with relapsed or refractory multiple myeloma after a lymphodepletion regimen with fludarabine and/or cyclophosphamide
Eligibility
Primary outcome measure(s)
- Occurrence of Dose Limiting Toxicities — Up to 36 days post-infusion.
Occurrence of Dose Limiting Toxicities
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| H. Lee Moffitt Cancer Center | Tampa | Florida | |
| Nyu Langone Hospitals | New York | New York | |
| Universitair Ziekenhuis Antwerpen | Antwerp | Belgium | |
| Institut Jules Bordet | Brussels | Belgium | |
| AZ DELTA | Roeselare | Belgium |
More Celyad Oncology SA trials in the USA
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04613557 on ClinicalTrials.gov ↗ ← All trials in the USA