Clinical trial · Interventional
Study of PD-1Ab21-BCMA CAR-T Therapy for Consolidation of Multiple Myelomawith Renal Dysfunction
Exploratory Clinical Study on PD-1Ab21-BCMA CAR-T Cells (CD203) for First-line Consolidation Therapy of Multiple Myeloma With Renal Dysfunction
NCT07489534CI-TRIAL-00106295recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- 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)
The purpose of this study is to determine the efficacy and safety of targeted BCMA CART cells secreting PD1 and interleukin 21 fusion protein immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction.
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 |
|---|---|---|---|
| PD-1Ab21-BCMA CAR-T cell immunotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- multiple myeloma patients with renal dysfunction who accept PD- 1Ab21-BCMA CAR-T cell immunotherapy
- interventionNames
- Drug: PD-1Ab21-BCMA CAR-T cell immunotherapy
Primary outcomes (1)
- measure
- 1-year progression free survival rate (1-year-PFS)
- timeFrame
- 1 year after treatment
- description
- The 1-year progression free survival rate (1-year-PFSR) of PD-1Ab21-BCMA CAR-T cell immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction refers to the proportion of disease progression that occurs within one year after treatment in patients.
Secondary outcomes (8)
- measure
- overall survival (OS)
- timeFrame
- 2 years after treatment
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 14 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age: Over 14 years old 2. Diagnosed with multiple myeloma accompanied by renal dysfunction, received ≥ 2 courses of clinical first-line treatment, evaluated efficacy above PR, and predicted survival of more than three months. 3. The hospital examination meets the following indicators: 1. ECOG physical status score 0-2 or KPS score\>80 points 2. Having sufficient venous access for single or intravenous blood collection, and no other blood cells Separation contraindications 3. WBC≥1×109/L,LY≥0.3×109/L, 4. ALT and AST ≤ 2.5 ULN 5. Serum total bilirubin ≤ 2.0mg/dL (34.2 μmol/L) 6. PT:INR\<1.7 or PT prolonged by\<4s compared to normal value Exclusion Criteria: 1. Pregnant or lactating women (the safety of this treatment for unborn babies is unknown, and the assessment of pregnancy status for female participants is negative in serum or urine pregnancy tests within 48 hours prior to infusion); 2. Any uncontrollable active infection; 3. Presence of active hepatitis B or C virus infection; 4. HIV/AIDS infection; 5. Has neurological disorders; 6. Within 2 weeks prior to signing the informed consent form, systemic use of steroid drugs (inhalable steroids may be used); 7. Allergies to immunotherapy and related drugs; 8. Currently, there are patients with heart disease or poorly controlled hypertension who require treatment; 9. Currently, patients with unstable or active ulcers or gastrointestinal bleeding; 10. Patients with a history of organ transplantation or waiting for organ transplantation; 11. Hyponatremia, blood sodium\<125mmol/L; 12. Baseline blood potassium\<3.5mmol/L (potassium can be supplemented before participating in the study to restore blood potassium levels above this level); 13. The patient needs anticoagulant therapy (such as warfarin or heparin); 14. The patient requires long-term antiplatelet therapy (aspirin, dose\>300mg/d); Clopidogrel, dose\>75mg/d). Additionally, 1. Patients currently participating in other clinical trials; 2. Researchers believe that other reasons are not suitable for clinical trial participants.
References
Publications (0)
Data not yet available
No reference posted for this study.