Clinical trial · Interventional
Study to Evaluate the Safety of UF-KURE-BCMA CAR T-Cells in Advanced Myeloma
A Phase 1, Single-Arm, Open-Label Study to Evaluate the Safety of UF-KURE-BCMA Cells in Patients With Relapsed or Refractory 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)
The goal of this study is to evaluate the safety of a new type of CAR T-cell, UF-KURE-BCMA, for the treatment of patients with advanced multiple myeloma that has not responded to other therapies. The main question is whether the use of these new CAR T-cells is safe for patients with this condition. Secondarily, the study will also look at the response of myeloma to this therapy.
Conditions
Conditions (2)
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 in Relapse | Multiple Myeloma | CURATED_BROADER | 0.78 |
| Multiple Myeloma, Refractory | Multiple Myeloma | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Administration of CAR T-cells at 3 different dose levels | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- ACTIVE_COMPARATOR
- label
- Lower Dose Level
- description
- Lower Dose (Level -1): 3 × 10⁶ cells (≥50 kg)// 2 × 10⁶ cells (\<50 kg)
- interventionNames
- Biological: Administration of CAR T-cells at 3 different dose levels
- type
- ACTIVE_COMPARATOR
- label
- Starting Dose Level
- description
- Starting Dose Level (Level 1) : 10 × 10⁶ cells (≥50 kg) / 7 × 10⁶ cells (\<50 kg)
- interventionNames
- Biological: Administration of CAR T-cells at 3 different dose levels
- type
- ACTIVE_COMPARATOR
- label
- Higher Dose Level
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Subjects must meet ALL of the following criteria to be eligible for study enrollment: 1. Age: ≥18 years at time of signing informed consent 2. Diagnosis: Documented multiple myeloma meeting one of the following: * Relapsed disease: Progression after achieving at least minimal response (MR) to prior therapy * Refractory disease: Non-responsive or progressive disease while on therapy or within 60 days of last treatment (in subjects who achieved ≥MR on prior therapy) 3. Prior Therapy: * Received ≥3 prior lines of anti-myeloma therapy * Prior therapy must include: At least one proteasome inhibitor At least one immunomodulatory drug (e.g., lenalidomide, pomalidomide, thalidomide) At least one anti-CD38 monoclonal antibody (e.g., daratumumab, isatuximab) o Prior anti-BCMA CAR-T therapy is permitted if subject achieved PFS ≥6 months post-infusion 4. Measurable Disease: At least one of the following at screening (for response assessment eligibility): * Serum M-protein ≥0.5 g/dL by protein electrophoresis (SPEP) * Urine M-protein ≥200 mg/24 hours by protein electrophoresis (UPEP) * Serum free light chain (FLC) difference ≥10 mg/dL with abnormal FLC ratio Note: Subjects with non-measurable disease may enroll for safety assessment 5. Performance Status: ECOG Performance Status 0-2 (see Appendix A) 6. Organ Function: Adequate organ function as defined by: Hepatic: o Total bilirubin ≤2× institutional upper limit of normal (ULN), except subjects with Gilbert's syndrome * AST and ALT ≤2.5× institutional ULN Renal: o Calculated creatinine clearance ≥30 mL/min (Cockcroft-Gault formula) Cardiac: o Left ventricular ejection fraction (LVEF) ≥45% by echocardiogram or MUGA Pulmonary: o ≤Grade 1 dyspnea o Oxygen saturation ≥92% on room air o If PFTs performed: FEV₁ ≥50% predicted and DLCO ≥40% predicted (corrected for hemoglobin) 7. Prior Therapy Washout: o ≥2 weeks since last radiation or systemic anti-myeloma therapy (standard agents) o ≥4 weeks since last investigational therapy o ≥6 weeks since autologous stem cell transplant 8. Informed Consent: Ability to understand and willingness to provide written informed consent 9. Contraception Requirements (for subjects of reproductive potential): Female subjects: o Women of childbearing potential must: Have negative serum pregnancy test at screening Agree to use highly effective contraception (failure rate \<1% per year) from enrollment through 6 months post-CAR-T infusion * Acceptable methods: bilateral tubal ligation, male partner sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing IUD, copper IUD * Sexual abstinence is acceptable if consistent with subject's preferred lifestyle Male subjects: * Must agree to use condom plus effective contraception if partner is of childbearing potential * Must refrain from sperm donation from enrollment through 6 months post-CAR-T infusion Exclusion Criteria: Subjects meeting ANY of the following criteria will be excluded: 1. Disease-Specific Exclusions: * Active CNS involvement by multiple myeloma * Plasma cell leukemia * History of allogeneic hematopoietic stem cell transplantation 2. Malignancy Exclusions: o Second active malignancy, except: Non-melanoma skin cancer Carcinoma in situ (cervix, bladder, breast) Stage 1 uterine cancer Localized prostate cancer 3. Cardiovascular Exclusions: * New York Heart Association (NYHA) Class IV congestive heart failure * Unstable angina pectoris * Clinically significant cardiac arrhythmias * Myocardial infarction, stroke, or TIA within 6 months of enrollment 4. Infectious Disease Exclusions: * Known HIV infection or AIDS-related illness * Active hepatitis B or C infection: Positive HBsAg, or Positive anti-HBc or anti-HCV with detectable viral nucleic acid by PCR * Active infection requiring systemic therapy 5. Neurological Exclusions: * History of clinically relevant CNS pathology including: Epilepsy or seizure disorders Paresis, aphasia Uncontrolled cerebrovascular disease Severe brain injury Dementia Parkinson's disease 6. Autoimmune Disease: * Active autoimmune disease requiring systemic immunosuppression \>15 mg/day prednisone equivalent within past 6 months * Examples: rheumatoid arthritis, lupus
References
Publications (8)
- BACKGROUNDMunshi NC, Anderson LD Jr, Shah N, Madduri D, Berdeja J, Lonial S, Raje N, Lin Y, Siegel D, Oriol A, Moreau P, Yakoub-Agha I, Delforge M, Cavo M, Einsele H, Goldschmidt H, Weisel K, Rambaldi A, Reece D, Petrocca F, Massaro M, Connarn JN, Kaiser S, Patel P, Huang L, Campbell TB, Hege K, San-Miguel J. Idecabtagene Vicleucel in Relapsed and Refractory Multiple Myeloma. N Engl J Med. 2021 Feb 25;384(8):705-716. doi: 10.1056/NEJMoa2024850. PMID 33626253
- RESULTHankey BF, Ries LA, Edwards BK. The surveillance, epidemiology, and end results program: a national resource. Cancer Epidemiol Biomarkers Prev. 1999 Dec;8(12):1117-21. No abstract available. PMID 10613347
- RESULTSan-Miguel J, Dhakal B, Yong K, Spencer A, Anguille S, Mateos MV, Fernandez de Larrea C, Martinez-Lopez J, Moreau P, Touzeau C, Leleu X, Avivi I, Cavo M, Ishida T, Kim SJ, Roeloffzen W, van de Donk NWCJ, Dytfeld D, Sidana S, Costa LJ, Oriol A, Popat R, Khan AM, Cohen YC, Ho PJ, Griffin J, Lendvai N, Lonardi C, Slaughter A, Schecter JM, Jackson CC, Connors K, Li K, Zudaire E, Chen D, Gilbert J, Yeh TM, Nagle S, Florendo E, Pacaud L, Patel N, Harrison SJ, Einsele H. Cilta-cel or Standard Care in Lenalidomide-Refractory Multiple Myeloma. N Engl J Med. 2023 Jul 27;389(4):335-347. doi: 10.1056/NEJMoa2303379. Epub 2023 Jun 5. PMID 37272512
- RESULTShah N, Chari A, Scott E, Mezzi K, Usmani SZ. B-cell maturation antigen (BCMA) in multiple myeloma: rationale for targeting and current therapeutic approaches. Leukemia. 2020 Apr;34(4):985-1005. doi: 10.1038/s41375-020-0734-z. Epub 2020 Feb 13. PMID 32055000
- RESULTGhassemi S, Durgin JS, Nunez-Cruz S, Patel J, Leferovich J, Pinzone M, Shen F, Cummins KD, Plesa G, Cantu VA, Reddy S, Bushman FD, Gill SI, O'Doherty U, O'Connor RS, Milone MC. Rapid manufacturing of non-activated potent CAR T cells. Nat Biomed Eng. 2022 Feb;6(2):118-128. doi: 10.1038/s41551-021-00842-6. Epub 2022 Feb 21. PMID 35190680
- RESULTRodriguez-Otero P, Ailawadhi S, Arnulf B, Patel K, Cavo M, Nooka AK, Manier S, Callander N, Costa LJ, Vij R, Bahlis NJ, Moreau P, Solomon SR, Delforge M, Berdeja J, Truppel-Hartmann A, Yang Z, Favre-Kontula L, Wu F, Piasecki J, Cook M, Giralt S. Ide-cel or Standard Regimens in Relapsed and Refractory Multiple Myeloma. N Engl J Med. 2023 Mar 16;388(11):1002-1014. doi: 10.1056/NEJMoa2213614. Epub 2023 Feb 10.