Clinical trial · Interventional
Safety and Efficacy of IM21 Car-t Cells in Patients With Recurrent or Refractory BCMA Positive Multiple Myeloma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In patients with multiple myeloma with recurrent or refractory BCMA, CAR-T cell infusion was performed after screening, blood collection and pretreatment. Starting dose for 5 x 10\^5 / kg, 1 x 10\^6 doses sequentially. If dose-limiting toxicity is not observed in 3 patients in a dose group, the next dose group test can be performed; If more than 2/3 of patients (2 cases, included) in a dose group had DLT, dose-escalation was not performed. If 1 case of DLT (1/3) appears in the first 3 patients of a dose group, 3 patients need to be added to the dose group (at this time, there are 6 patients in the group).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IM21 CAR-T cells | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- IM21 CAR-T cells
- description
- IM21 CAR-T cells
- interventionNames
- Biological: IM21 CAR-T cells
Primary outcomes (1)
- measure
- Occurrence of study related adverse events
- timeFrame
- 2 years
- description
- defined as \>= Grade 3 signs/symptoms, laboratory toxicities, and clinical events) that are possibly, likely, or definitely related to study treatment Adverse events assessed according to NCI-CTCAE v4.0 criteria 2.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. The patient had multiple myeloma (according to the updated IMWG diagnostic criteria)Active (symptomatic) myeloma 2. Refractory and recurrent multiple myeloma Refractory definition: 1) treated with at least second-line bortezomib or lenalidomide 2) determined by the clinician Definition of recurrence: refer to NCCN clinical guidelines for multiple myeloma (2016. V2), including recurrence after transplantation. 3. Age: 18 to 80 years old; 4. The expected survival time was more than 3 months; 5. ECoG score 0-2 (refer to Annex 2) 6. Hemoglobin (HB)≥80g/L; absolute neutrophil count (ANC)\>1×10\^9/L; platelet count(PLT)≥50×10\^9/L. Those who voluntarily participated in the experiment and signed informed consent. Exclusion Criteria: 1. High risk organ involvement patients: tumor invasion of central nervous system, gastrointestinal tract,lung,pericardium,one of the major vessels; 2. Those who have graft-versus-host reaction and need to use immunosuppressants, or who have autoimmune diseases; 3. Chemotherapy or radiotherapy was used within 3 days before blood collection; 4. Patients who used systemic steroids within 5 days before blood collection (except those who have recently or are currently using inhaled steroids); 5. The patients who used drugs to stimulate the production of bone marrow hematopoietic cells within 5 days before the blood collection period; 6. Those who have previously used any gene therapy products; 7. History of epilepsy or other central nervous system diseases; 8. New York Heart Association (NYHA) grade III or above (refer to Annex 3) (for patients with heart disease, this assessment is required); 9. Creatinine \> 1.5 times normal upper limit, ALT / AST\>3 times normal upper limit or bilirubin \>2 times normal upper limit; 10. Active hepatitis B or hepatitis C virus, HIV or other uncured active infections; 11. Pregnant or lactating women; 12. Those who suffer from other uncontrolled diseases are not suitable to join the study; Any situation that the researchers believe may increase the risk of subjects or interfere with the test results.
References
Publications (0)
Data not yet available