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Study identifier: NCT07139509 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Allogeneic UCB-derived, Dual-targeting BCMA/CD19 CAR-T for Relapsed/Refractory Multiple Myeloma

Condition: Relapsed/Refractory Multiple Myeloma(MM)  ·  Sponsor: Xi'an No.3 Hospital

PhasePhase 1
Planned participants18
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The purpose of this clinical trial is to learn if allogeneic cord blood-derived CAR-T cell drug works to treat Multiple Myeloma (MM) including Bone-related extramedullary (EMB) disease and extramedullary extraosseous disease(EME) in adults. It will also learn about the safety of the allogeneic cord blood-derived CAR-T cell drug. The main questions it aims to answer are: 1. What adverse events occur and the incidence rate of DLTs within 28 days and UCAR-T-related AEs within 28 days after the allogeneic cord blood-derived CAR-T cell injection for multiple myeloma (MM)? 2. Which dose level is the optimal biological dose (OBD)? 3. What is the overall responserate (ORR), including stringent complete response (sCR), completeresponse (CR),very good partial response (VGPR), partial response (PR), minimal Response (MR) and DOR, PFS, RFS, OS? Participants will: 1. be pretreated with FC regimen, fludarabine (30mg/m²/d, days -5, -4, and -3) and cyclophosphamide (300\~500 mg/m²/d, day -5,-4, and -3). 2. rest for 2 days on Day-2 and Day-1. Tumor burden should be re-evaluated and chemotherapy side effects assessment. 3. receive allogeneic cord blood-derived CAR-T cells infusion 4. Visit the clinic at D28, 1 month, 2 months, 3 months, 4 months, 6 months, 9 months and 1 year after CAR-T cells infusion.

This description comes directly from the study's public registry record.

Talk to the study team

Xiequn Chen, M.D.  ·  +86 29 6130 6285  ·  cxq@nwu.edu.cn

Qiang Zou, Ph.D. & M.D.  ·  86-18908237461  ·  zouqiang@ucellotx.com

Always discuss trial participation with your own doctor first.

Locations (1)

Xi'an No.3 HospitalXi’an, Shanxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07139509