- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07759102
Allogeneic ORCA-Q Stem Cell Transplant for the Treatment of Relapsed and Refractory High Risk Multiple Myeloma
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
Descripción general del estudio
Estado
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
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Office of Clinical Research
- Número de teléfono: 916-382-6970
- Correo electrónico: OCRReferral@health.ucdavis.edu
Ubicaciones de estudio
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California
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Sacramento, California, Estados Unidos, 95817
- University of California Davis Comprehensive Cancer Center
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Investigador principal:
- Mehrdad Abedi, MD
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Contacto:
- Office of Clinical Research
- Número de teléfono: 916-382-6970
- Correo electrónico: OCRReferral@health.ucdavis.edu
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
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
¿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 |
|---|---|
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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.
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Dado IV
Otros nombres:
Dado SC
Otros nombres:
Dado IV
Otros nombres:
Dado IV
Otros nombres:
Dado SC
Otros nombres:
Given Orca-Q prime IV
Otros nombres:
Given Orca-Q supplement IV
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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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
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Frequency and proportions will be obtained.
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From date of transplant and up to 30 days post-transplant
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Overall survival
Periodo de tiempo: From transplant to death from any cause, assessed up to day 365 post-transplant
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The Kaplan-Meier (KM) method will be used to estimate the median and percentiles for time-to-event endpoints with 95% confidence intervals (CIs).
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From transplant to death from any cause, assessed up to day 365 post-transplant
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Progression-free survival
Periodo de tiempo: From transplant to progressive disease or death, assessed up to 365 days post-transplant
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The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
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From transplant to progressive disease or death, assessed up to 365 days post-transplant
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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
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From transplant to disease progression, initiation of new anti-multiple myeloma treatment, or death, whichever occurs first, assessed up to 365 days post-transplant
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Non-relapse mortality
Periodo de tiempo: From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
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Will be analyzed using the cumulative incidence function to account for the competing risk of disease relapse/progression.
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From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
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Number of treatment-related adverse events (AEs)
Periodo de tiempo: From date of enrollment up to 100 days post-transplant
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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.
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From date of enrollment up to 100 days post-transplant
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Occurrence of grade 3 or 4 treatment-emergent AEs
Periodo de tiempo: From date of transplant up to 100 days post-transplant
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Will be classified by severity and graded according to the NCI CTCAE v 6.0.
Frequency and proportions will be obtained.
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From date of transplant up to 100 days post-transplant
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Incidence of acute GVHD
Periodo de tiempo: From date of transplant up to 100 days post-transplant
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From date of transplant up to 100 days post-transplant
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Incidence of chronic GVHD
Periodo de tiempo: From date of transplant up to 100 days post-transplant
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From date of transplant up to 100 days post-transplant
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Incidence of GVHD free, relapse free survival
Periodo de tiempo: From date of transplant up to 365 days post-transplant
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The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
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From date of transplant up to 365 days post-transplant
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Secondary graft failure rate
Periodo de tiempo: Up to day 365 post-transplant
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Up to day 365 post-transplant
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mehrdad Abedi, University of California, Davis
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades Vasculares
- Enfermedades cardiovasculares
- Neoplasias
- Enfermedades del sistema inmunológico
- Neoplasias por tipo histológico
- Enfermedades hematológicas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Neoplasias De Células Plasmáticas
- Trastornos hemostáticos
- Paraproteinemias
- Trastornos de proteínas en sangre
- Trastornos hemorrágicos
- Enfermedades hemic y linfáticas
- Mieloma múltiple
- Péptidos
- Aminoácidos, péptidos y proteínas
- Proteínas
- Compuestos de azufre
- Químicos orgánicos
- Compuestos heterocíclicos, 1 anillo
- Compuestos heterocíclicos
- Hidrocarburos, acíclico
- Hidrocarburos
- Factores biológicos
- Carbohidratos
- Alcanos
- Alcoholes
- Butilenglicoles
- Glicolos
- Mesilatos
- Alcanosulfonatos
- Ácidos alcanosulfónicos
- Ácidos sulfónicos
- Ácidos de azufre
- Fosforamidas
- Compuestos organofosforados
- Péptidos de señalización intercelular y proteínas
- Glicoproteínas
- Glucoconjugados
- Trietilenefosforamida
- Aziridinas
- Azirines
- Factores estimulantes de colonias
- Factores de crecimiento de células hematopoyéticas
- Citocinas
- Busulfán
- Tiotepa
- fludarabina
- Factor estimulador de colonias de granulocitos
- Filgrastim
Otros números de identificación del estudio
- UCDCC330 (Otro identificador: University of California Davis Comprehensive Cancer Center)
- P30CA093373 (Subvención/contrato del NIH de EE. UU.)
- NCI-2026-05456 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .