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Clinical Trial 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


Clinical Trial Description

This study aims to determine the recommended dose of the allogeneic CYAD-211 (anti-BCMA CAR-T) cells after a non-myeloablative preconditioning chemotherapy in multiple myeloma (MM) patients with relapsed or refractory disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04613557
Study type Interventional
Source Celyad Oncology SA
Contact
Status Active, not recruiting
Phase Phase 1
Start date November 16, 2020
Completion date February 2037

See also
  Status Clinical Trial Phase
Completed NCT03944057 - A Study of Evaluating the Safety and Efficacy of ATG-010 in Relapsed Refractory Multiple Myeloma Phase 2
Recruiting NCT06084962 - A Study of DeepTag-GPRC5D Targeted CAR-T Cells Therapy for Refractory/Relapsed Multiple Myeloma Phase 1
Completed NCT03353545 - Retrospective and Prospective Study of POmalidomide Plus LoW Dose Dexa Efficacy in RRMM Patients Under Real-Life Conditions
Withdrawn NCT02985333 - Paclitaxel,Cyclophosphamide and Dexamethasone for Relapsed or Refractory Multiple Myeloma Phase 2
Withdrawn NCT02986451 - Clarithromycin,Lenalidomide and Dexamethasone for Relapsed/Refractory Myeloma Phase 2
Completed NCT02290431 - Study of Panobinostat in Combination With Bortezomib and Dexamethasone in Japanese Patients With Relapsed/Refractory Multiple Myeloma Phase 2