- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07844694
Low-Dose Sirolimus for the Treatment of RUNX1 Familial Platelet Disorder
Low-Dose Sirolimus to Increase Hematopoietic Function in Patients With RUNX1 Familial Platelet Disorder - Part II
This phase I trial studies the safety and side effects of low-dose sirolimus in treating patients with RUNX1 familial platelet disorder (FPD). RUNX1-FPD is a rare inherited disorder with symptoms such as mild to moderately low platelet count, abnormal platelet function, and an increased risk of developing cancers like myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). It is caused by changes (variants) in the RUNX1 gene that is passed down (inherited) from an affected parent. Sirolimus is typically given to help prevent organ rejection in patients receiving kidney transplants. However, sirolimus may also be able to prevent RUNX1-FPD from progressing to cancers like MDS and AML by targeting another protein called mTORC1. Sirolimus may be a safe treatment for patients with RUNX1-FPD.
Descripción general del estudio
Estado
Descripción detallada
PRIMARY OBJECTIVE:
I. Evaluate the safety and tolerability of low-dose sirolimus in patients with RUNX1 familial platelet disorder (RUNX1-FPD).
SECONDARY OBJECTIVES:
I. Evaluate platelet counts. II. Evaluate changes in somatic mutation variant allele frequency (VAF). III. Evaluate somatic mutation acquisition (i.e., mutation burden). IV. Evaluate the change in platelet function. V. Evaluate the change from baseline in bleeding score (International Society on Thrombosis and Haemostasis Bleeding Assessment Tool [ISTH-BAT]).
VI. Evaluate the change in mTORC1 downstream signaling.
EXPLORATORY OBJECTIVES:
I. Evaluate the rescue of elevated cytokine profiles. II. Evaluate the reversal of myeloid skewing using colony formation assay. III. Evaluate monocytes using clinical flow cytometry. IV. Evaluate changes in patient-reported quality of life (QoL) outcomes measures (e.g., Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events [PRO-CTCAE]).
V. Determine the pharmacokinetics of sirolimus in participants with RUNX1-FPD. VI. Evaluate the correlation between sirolimus trough levels and each endpoint. VII. Make bone marrow smears and bone marrow biopsy slides. VIII. Evaluate the cellularity of bone marrow after study treatment.
OUTLINE:
Patients receive sirolimus orally (PO) once daily (QD) on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study.
After completion of study treatment, patients are followed for 6 months.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Knight Cancer Institute Clinical Trials Information
- Número de teléfono: 503-494-1080
- Correo electrónico: trials@ohsu.edu
Ubicaciones de estudio
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Oregon
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Portland, Oregon, Estados Unidos, 97239
- Reclutamiento
- OHSU Knight Cancer Institute
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Investigador principal:
- Curtis A. Lachowiez
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Contacto:
- Knight Cancer Institute Clinical Trials Information
- Número de teléfono: 503-494-1080
- Correo electrónico: trials@ohsu.edu
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Patient has provided signed, informed consent before initiation of any study specific procedures
- Aged ≥ 18 years at the time of signing the informed consent
- Confirmed pathogenic/likely pathogenic (P/LP) germline RUNX1 variant per ClinGen Myeloid Malignancy Variant Curation Expert Panel (MM-VCEP) RUNX1-specific variant curation rules
- Patient must be willing to provide a bone marrow sample at time of screening and at the end of treatment with sirolimus
- Platelet count of ≥ 50,000/µL
- Creatinine clearance (CrCl) of ≥ 60 mL/min; estimated using the Cockcroft Gault formula or measured by 24 hour urine collection. Exceptions will be allowed, at the discretion of the investigator, for cases of a concomitant medication that alters renal function
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 3 × upper limit of normal (ULN)
- Total bilirubin < 1.5 × ULN
- Left ventricular ejection fraction (EF) > 50% or at the discretion of the investigator
Exclusion Criteria:
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Known allergy to sirolimus
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History of major bleeding events that are clinically relevant in the judgement of the investigator or non-major bleeding events that cannot be controlled using SOC practices
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Any known history of lymphoma, myelodysplastic syndrome (MDS), or other hematologic malignancy using International Working Group criteria
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Prior treatment with sirolimus or a rapalog, mTOR inhibitor, or B-cell-depleting therapy within 28 days before study day 1
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Treatment with strong inhibitors of cytochrome P450 3A4 (CYP3A4; e.g., ketoconazole, voriconazole, itraconazole, erythromycin, telithromycin, and clarithromycin), strong inducers of CYP3A4 (e.g., rifampin and rifabutin), other drugs that could increase sirolimus blood concentrations (e.g., bromocriptine, cimetidine, cisapride, clotrimazole, danazol, diltiazem, fluconazole, letermovir, protease inhibitors [e.g., ritonavir, indinavir, boceprevir, and telaprevir], metoclopramide, nicardipine, troleandomycin, and verapamil), other drugs that could decrease sirolimus blood concentrations (e.g., carbamazepine, phenobarbital, phenytoin, rifapentine, St. John's Wort [Hypericum perforatum]), or drugs with blood concentrations that could increase (e.g., verapamil) within 7 days before study day 1, or at the discretion of the investigator
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Use of cannabidiols that increase blood levels of sirolimus, within 7 days before study day 1 or at the discretion of the investigator
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Myocardial infarction within 6 months before study day 1, congestive heart failure (New York Heart Association > class II)
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Total cholesterol > 300 mg/dL or triglyceride > 400 mg/dL
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Arterial thrombosis (e.g., stroke or transient ischemic attack) within 6 months before study day 1
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Infection requiring intravenous anti-infective treatment within 1 week of study day 1
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Live vaccines (e.g., measles, mumps, rubella, oral polio, Bacillus Calmette-Guerin [BCG], yellow fever, varicella, and TY21a typhoid) within 28 days before study day 1
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Known diagnosis of tuberculosis is exclusionary to provide protection against reactivation of infections by the immunosuppressive activity of the study drug sirolimus
- The enrollment of a patient with a history of infection with hepatitis B virus (HBV) but with undetectable HBV deoxyribonucleic acid (DNA) by standard institutional testing can be considered after consultation with the investigator
- Patients with history of chronic hepatitis C virus (HCV) must have documentation of completed curative standard of care (SOC) antiviral therapy
- Patients with history of HIV infection must be well-managed with SOC antiretroviral therapy (highly active antiretroviral therapy [HAART])
- Patients with history of Epstein-Barr may be considered after consultation with the treating physician
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Participants who are pregnant may become pregnant, or who are breastfeeding
- Because adequate and well-controlled studies of the impact of sirolimus on fetuses currently do not exist, study approved contraception must be used from start of study therapy to 12 weeks after the last dose of sirolimus
- Adequate and well-controlled studies of infants fed breastmilk from patients undergoing sirolimus therapy do not exist and breastfeeding during study treatment is prohibited
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 (sirolimus)
Patients receive sirolimus PO QD on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study. |
Ancillary studies Undergo collection of blood
Otros nombres:
Undergo bone marrow biopsy/aspiration Undergo bone marrow biopsy/aspiration
Otros nombres:
Given PO
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 grade 3+ treatment-related adverse events (TRAEs)
Periodo de tiempo: From study day 1 (week 1) to 30 days after the last dose of sirolimus
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The incidence of grade 3+ TRAEs and the total proportion of participants who experienced grade 3+ TRAEs will be estimated and presented with the corresponding 95% exact Clopper Pearson confidence intervals. |
From study day 1 (week 1) to 30 days after the last dose of sirolimus
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in platelet count
Periodo de tiempo: From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)
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Change in variant allele frequency for existing clones
Periodo de tiempo: From screening to end of study (EOS) (week 52, day 365)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening to end of study (EOS) (week 52, day 365)
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Change in number of clonal hematopoiesis of indeterminate potential mutations
Periodo de tiempo: From screening to EOS (week 52, day 365)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening to EOS (week 52, day 365)
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Change in percent positivity based on activated GPIIb IIIa and surface P selectin and CD42b
Periodo de tiempo: From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
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Change in aggregation from baseline based on thromboelastography (TEG)
Periodo de tiempo: From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
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Change in the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool score
Periodo de tiempo: From study day 1 (week 1) to EOS (week 52, day 365)
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Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From study day 1 (week 1) to EOS (week 52, day 365)
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Change in the relative amount of the protein 4eBP1
Periodo de tiempo: From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)
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Will be based on flow cytometry and immunohistochemistry assays. Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented. |
From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Curtis A Lachowiez, OHSU Knight Cancer Institute
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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
Términos MeSH relevantes adicionales
- Trastorno de plaquetas, familiar, con malignidad mieloide asociada
- Químicos orgánicos
- Técnicas de investigación
- Técnicas de laboratorio clínico
- Técnicas y procedimientos de diagnóstico
- Diagnóstico
- Procedimientos quirúrgicos, operativo
- Técnicas citológicas
- Citodiagnóstico
- Técnicas de diagnóstico, quirúrgico
- Macrólidos
- Lactonas
- Sirolimus
- Biopsia
- Manejo de muestras
Otros números de identificación del estudio
- STUDY00028610
- P30CA069533 (Subvención/contrato del NIH de EE. UU.)
- NCI-2026-03902 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
- STUDY00028610 (Otro identificador: OHSU Knight Cancer Institute)
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. .