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Allogeneic ORCA-Q Stem Cell Transplant for the Treatment of Relapsed and Refractory High Risk Multiple Myeloma

5 de agosto de 2026 actualizado por: University of California, Davis

A Phase I Study to Evaluate the Safety and Efficacy of ORCA-Q Allogeneic Hematopoietic Stem Cell Transplantation for the Treatment of Relapsed/ Refractory High Risk Multiple Myeloma

This phase I trial tests the effect of allogeneic Orca-Q stem cell transplant in treating patients with high-risk multiple myeloma that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). An allogeneic (donor) transplant uses blood forming stem cells (graft) from a matched donor. When the healthy blood forming (stem) cells from a donor are infused into a patient, they may help the patient's bone marrow make more healthy cells and platelets and may help destroy any remaining cancer cells. Sometimes the transplanted cells from a donor can attack the body's normal cells (called graft-versus-host disease [GVHD]). Orca-Q includes some T cells (a type a white blood cell) that are thought to help prevent some of the known complications as well as help attack the cancer cells. However, Orca-Q removes a specific type of T cell called naive T lymphocytes. Naive T cells may contribute to GVHD and are not thought to be required for the success of the treatment. Removing these cells may help reduce the frequency or severity of GVHD. Giving chemotherapy, such as thiotepa, busulfan, and fludarabine, before a donor stem cell transplant helps kill cancer cells in the body and prepare the body to receive the transplant graft. Giving allogeneic Orca-Q may be safe, tolerable, and/or effective in treating patients with relapsed or refractory (R/R) high-risk multiple myeloma.

Descripción general del estudio

Descripción detallada

PRIMARY OBJECTIVE:

I. To evaluate the safety of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

SECONDARY OBJECTIVES:

I. To evaluate the efficacy of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

II. To further evaluate the safety of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

EXPLORATORY OBJECTIVE:

I. To further evaluate the efficacy of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

OUTLINE:

DONORS: Donors receive granulocyte colony-stimulating factor (G-CSF) or filgrastim subcutaneously (SC) daily (QD) on days -6 to -3 and undergo apheresis on day -2 or -1. Donors may also undergo a second apheresis on day -1 or 0. Additionally, donors undergo blood sample collection at screening.

PATIENTS: Patients receive thiotepa intravenously (IV) over 3 hours on days -7 and -6, busulfan IV over 3 hours on days -5 to -3, fludarabine IV over 30 minutes on days -5 to -2, Orca-Q prime IV on day 0 followed by Orca-Q supplement IV on day 0 or 1 in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo echocardiography or multigated acquisition scan (MUGA) and optional positron emission tomography (PET)/computed tomography (CT) or CT at screening and urine and blood sample collection, as well as bone marrow aspiration and biopsy throughout the study.

After completion of study treatment, patients are followed up on days 1-7, 14, 21, 30, 60, 90, 180, and 365.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

20

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • California
      • Sacramento, California, Estados Unidos, 95817
        • University of California Davis Comprehensive Cancer Center
        • Investigador principal:
          • Mehrdad Abedi, MD
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Ability to understand and sign informed consent
  • Age ≥ 18 years and ≤ 65 years
  • Patients should be in very good partial response (VGPR) (5% or less plasma cells in the marrow) or better response status at the time of stem cell transplant with no evidence of central nervous system (CNS) disease. Patients in complete response (CR) should have minimal residual disease (MRD) positivity
  • Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1; or Karnofsky performance status (KPS) of ≥ 70%
  • ≥ 60 days washout period from the last dose of an anti-CD38 antibody before the allogeneic transplant
  • ≥ 6 months washout period from the last autologous transplant before the allogeneic transplant
  • Related or unrelated donors available as follows:

    • Sibling donor who is a 7/8 mismatched or 8/8 matched for human leukocyte antigen (HLA)-A, -B, -C, -DRB1
    • Matched unrelated donor who is a 7/8 mismatched or 8/8 matched for HLA-A, -B, -C, and -DRB1
  • A diagnosis of relapsed or refractory defined as:

    • Primary refractory disease or relapse < 12 months following initial therapy that includes an immunomodulatory agent, proteasome inhibitor, anti-CD38 monoclonal antibody, and corticosteroid
    • Relapse < 12 months after first autologous stem cell transplant
    • Failing to achieve complete response or relapsing after chimeric antigen receptor (CAR)-T treatment or bispecific antibodies; or indicated but ineligible for either bispecific antibodies or CAR-T cells due to low blood counts
    • No appropriate standard of care therapy per investigator
  • A diagnosis of ultra-high risk multiple myeloma defined as having at least one or more of these criteria:

    • Biallelic TP53 inactivation
    • ≥ 2 HRCAs: del(17p), TP53 mutation, t(4;14), t(14;16), t(14;20), gain(1q), amp(1q), del(1p32)
    • Biallelic del(1p32)
    • High-risk gene expression profile signature
    • Extramedullary disease excluding intramedullary plasmacytoma with extraosseous extension and active CNS disease
    • ≥ 2% circulating plasma cells
  • Creatinine clearance of ≥ 50 mL/min as estimated by Cockcroft-Gault
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN) except in subjects with Gilbert's syndrome in whom total bilirubin ≤ 3 times ULN
  • Alanine transaminase (ALT/serum glutamic pyruvic transaminase [SGPT]) and aspartate aminotransferase (AST/serum glutamic oxaloacetic transaminase [SGOT]) ≤ 3 x the upper limit of normal (ULN) or ≤ 5 x ULN if documented liver involvement by disease
  • Estimated glomerular filtration rate (eGFR) > 50mL/minute. Creatinine clearance of ≥ 30 mL/min is allowed in patients eligible for no tacrolimus immunosuppression
  • Pulmonary function as defined by diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50%
  • Cardiac ejection fraction at rest ≥ 45% or shortening fraction of ≥ 27% by echocardiogram, or radionuclide scan (multigated acquisition scan [MUGA])
  • Corrected diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50%
  • Individuals of childbearing potential or those with partners of childbearing potential must agree to use methods of contraception for the duration of study participation or be surgically sterilized
  • Stated ability and willingness to adhere to the study visit schedule and protocol requirements
  • DONOR: Ability to understand and sign informed consent
  • DONOR: Age ≥ 16 and ≤ 35 years at time of enrollment for unrelated donors and Age ≥ 16 and ≤ 50 years for related donors
  • DONOR: Either one of the following scenarios:

    • Sibling donor who is a 7/8 mismatched or 8/8 matched for HLA-A, -B, -C, and -DRB1, all typed using deoxyribonucleic acid (DNA)-based high-resolution methods
    • Unrelated donor who is 7/8 mismatched or 8/8 matched HLA-A, -B, -C, and -DRB1, all typed using DNA-based high-resolution methods
  • DONOR: Willing to donate stem cell mobilized mononuclear cells for up to two consecutive days
  • DONOR: Able to donate within the continental United States at a site that will employ a Spectra Optia Apheresis System for post-mobilization apheresis
  • DONOR: Meets federal eligibility criteria for donors of viable, leukocyte-rich cells or tissues and all relevant Food and Drug Administration (FDA) Guidance for Industry (Eligibility Determination for Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products, 2007; Use of Donor Screening Tests to Test Donors of Human Cells, Tissues and Cellular and Tissue-Based Products for Infection with Treponema pallidum [syphilis], 2015; Use of Nucleic Acid Tests to Reduce the Risk of Transmission of Hepatitis B Virus from Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products, 2016; Use of Nucleic Acid Tests to Reduce the Risk of Transmission of West Nile Virus from Living Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products [HCT/Ps], 2016)
  • DONOR: Donors determined to be ineligible, based on the results of required testing and/or screening, may nonetheless be included if either applies:

    • The donor is a first-degree blood relative of the recipient
    • Urgent medical need, meaning no comparable human cell product is available, and the recipient is likely to suffer death or serious morbidity without the human cell product, as attested by the investigator
    • Meets any other criteria for donation as specified by standard National Marrow Donor Program (NMDP) guidelines (NMDP donors) or institutional standards (non-NMDP donors)

Exclusion Criteria:

  • Prior allogeneic hematopoietic cell transplantation (HCT)
  • Planned pharmaceutical in vivo or ex vivo T cell depletion, e.g., post-transplant cyclophosphamide (Cy), peri-transplant anti-thymocyte globulin (ATG), or alemtuzumab
  • Positive anti-donor HLA antibodies against a mismatched allele in the selected donor determined by either:

    • A positive crossmatch test of any titer; or
    • The presence of anti-donor HLA antibody to any HLA locus
  • Hematopoietic cell transplantation-specific Comorbidity Index (HCT-CI) > 4
  • Uncontrolled bacterial, viral, or fungal infections (currently taking antimicrobial therapy and with no clinical improvement) at time of enrollment
  • Seropositive for HIV-1 or -2, human T-cell lymphotropic virus (HTLV)-1 or -2
  • Documented allergy or documented hypersensitivity to iron dextran or bovine, murine, algal or Streptomyces avidinii proteins
  • Concurrent malignancies or active disease within 1 year, except non-melanoma skin cancers or any carcinoma in situ that have been curatively resected
  • History of idiopathic or secondary myelofibrosis
  • Individuals who are pregnant or breastfeeding
  • Any condition that would prohibit the understanding or rendering of informed consent
  • Any condition that in the opinion of the investigator would interfere with the subject's safety or compliance while on study
  • A diagnosis of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome
  • DONOR: Evidence of uncontrolled, active infection
  • DONOR: Seropositive for HIV-1 or -2, HTLV-1 or -2
  • DONOR: Positive for hepatitis B (HBV) surface antigen (HBsAg), total anti-hepatitis B core antibody (HBcAb, immunoglobulin [I]gG and IgM), HBV nucleic acid testing (NAT), anti-hepatitis C (HCV) antibody, or HCV NAT
  • DONOR: Aberrant CD45RA isoform expression
  • DONOR: Women who are pregnant or breastfeeding

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment (Orca-Q, thiotepa, busulfan, fludarabine)
Recipient participants receive thiotepa IV over 3 hours on days -7 and -6, busulfan IV over 3 hours on days -5 to -3, fludarabine IV over 30 minutes on days -5 to -2, Orca-Q prime IV on day 0, followed by Orca-Q supplement IV on day 0 or 1 in the absence of disease progression or unacceptable toxicity.
Dado IV
Otros nombres:
  • Fluradosa
Dado SC
Otros nombres:
  • G-CSF
  • r-metHuG-CSF
  • Neupogen
  • Filgrastim-aafi
  • Nivestym
  • Factor estimulante de colonias de granulocitos humanos de metionilo recombinante
  • rG-CSF
  • Tevagrastim
  • Filgrastim Biosimilar Filgrastim-sndz
  • Zarxio
  • Filgrastim XM02
  • Tbo-filgrastim
  • Granix
  • Nivestim
  • XM02
  • Filgrastim-sndz
  • Filgrastim Biosimilar Tbo-filgrastim
  • Filgrastim-ayow
  • Releuco
  • Neutroval
Dado IV
Otros nombres:
  • Busulfex
  • Misulfán
  • Mitosan
  • Mieloleucona
  • Mielosana
  • 1, 4-bis[metanosulfonoxi]butano
  • AUTOBÚS
  • Bussulfam
  • Busulfano
  • Busulfán
  • CB 2041
  • CB-2041
  • Glyzophrol
  • GT 41
  • GT-41
  • Joaquín
  • Éster de tetrametileno del ácido metanosulfónico
  • Ácido metanosulfónico, éster de tetrametileno
  • Mielucin
  • Misulban
  • Mieleukon
  • Milecitano
  • Myleran
  • Sulfabutina
  • Bis(metanosulfonato) de tetrametileno
  • Bis[metanosulfonato] de tetrametileno
  • WR-19508
  • Busilvex
Dado IV
Otros nombres:
  • Tepadina
  • Oncotiotepa
  • PASO
  • Tespa
  • Tespamina
  • TSPA
  • 1,1',1''-fosfinotioilidinatrisaziridina
  • Girostán
  • N,N',N''-trietilentiofosforamida
  • Tio-tepa
  • Tiofosfamida
  • Tiofozilo
  • Tiofosforamida
  • Tiotef
  • Tifosilo
  • TÍO TEF
  • Tio-tef
  • Trietilen tiofosforamida
  • Trietilentiofosforamida
  • Sulfuro de tris(1-aziridinil)fosfina
  • WR 45312
  • Tiofosfoamida
  • SH-105
  • SH105
  • Tepilute
Dado SC
Otros nombres:
  • G-CSF
  • Factor estimulante de colonias de granulocitos
  • GCSF
  • Factor estimulante de colonias 3
  • Factor estimulante de colonias (granulocitos)
  • LCR3
  • LCR
  • Pluripoyetina
Given Orca-Q prime IV
Otros nombres:
  • Allogeneic Defined HSCs/Immune Cells
  • Allogeneic Defined Stem and Immune Cells
  • Orca-Q
Given Orca-Q supplement IV
Otros nombres:
  • Allogeneic Defined HSCs/Immune Cells
  • Allogeneic Defined Stem and Immune Cells
  • Orca-Q

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of primary graft failure without grade II-IV acute graft-versus-host disease (GVHD)
Periodo de tiempo: From date of transplant and up to 30 days post-transplant
Frequency and proportions will be obtained.
From date of transplant and up to 30 days post-transplant

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall survival
Periodo de tiempo: From transplant to death from any cause, assessed up to day 365 post-transplant
The Kaplan-Meier (KM) method will be used to estimate the median and percentiles for time-to-event endpoints with 95% confidence intervals (CIs).
From transplant to death from any cause, assessed up to day 365 post-transplant
Progression-free survival
Periodo de tiempo: From transplant to progressive disease or death, assessed up to 365 days post-transplant
The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
From transplant to progressive disease or death, assessed up to 365 days post-transplant
Time to relapse
Periodo de tiempo: From transplant to disease progression, initiation of new anti-multiple myeloma treatment, or death, whichever occurs first, assessed up to 365 days post-transplant
From transplant to disease progression, initiation of new anti-multiple myeloma treatment, or death, whichever occurs first, assessed up to 365 days post-transplant
Non-relapse mortality
Periodo de tiempo: From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
Will be analyzed using the cumulative incidence function to account for the competing risk of disease relapse/progression.
From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
Number of treatment-related adverse events (AEs)
Periodo de tiempo: From date of enrollment up to 100 days post-transplant
Will be classified by severity and graded according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 6.0. Frequency and proportions will be obtained.
From date of enrollment up to 100 days post-transplant
Occurrence of grade 3 or 4 treatment-emergent AEs
Periodo de tiempo: From date of transplant up to 100 days post-transplant
Will be classified by severity and graded according to the NCI CTCAE v 6.0. Frequency and proportions will be obtained.
From date of transplant up to 100 days post-transplant
Incidence of acute GVHD
Periodo de tiempo: From date of transplant up to 100 days post-transplant
From date of transplant up to 100 days post-transplant
Incidence of chronic GVHD
Periodo de tiempo: From date of transplant up to 100 days post-transplant
From date of transplant up to 100 days post-transplant
Incidence of GVHD free, relapse free survival
Periodo de tiempo: From date of transplant up to 365 days post-transplant
The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
From date of transplant up to 365 days post-transplant
Secondary graft failure rate
Periodo de tiempo: Up to day 365 post-transplant
Up to day 365 post-transplant

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Mehrdad Abedi, University of California, Davis

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de septiembre de 2032

Finalización del estudio (Estimado)

1 de septiembre de 2033

Fechas de registro del estudio

Enviado por primera vez

5 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de agosto de 2026

Publicado por primera vez (Actual)

12 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

5 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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