- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07719127
Study of Disulfiram to Reduce Myeloid Immunosuppression and Steroid Dependence in Resectable High Grade Glioma
A Window-of-Opportunity Study of Disulfiram to Reduce Myeloid Immunosuppression and Steroid Dependence in Resectable High-Grade Glioma
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Glioblastoma is one of the most common brain cancers that affect adults and is very hard to treat. This is due to myeloid cells, which are special immune cells in the body that prevent the body from recognizing and attacking the tumor. Because of this, immunotherapies have not worked well in treating glioblastoma.
Disulfiram may also reduce brain swelling, which may decrease or delay the need for subjects to be treated with steroids.
The purpose of this study is to find out if disulfiram can help reduce immunosuppression and help prevent edema symptoms when taken 3-14 days before planned surgery.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Tiffany Hodges, MD
- Número de teléfono: 216-286-7122
- Correo electrónico: tiffany.hodges@uhhospitals.org
Ubicaciones de estudio
-
-
Ohio
-
Cleveland, Ohio, Estados Unidos, 44106
- University Hospitals Cleveland Medical Center
-
Contacto:
- Tiffany Hodges, MD
- Número de teléfono: 216-286-7122
- Correo electrónico: tiffany.hodges@uhhospitals.org
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥18 years.
- Radiographically suspected or confirmed high-grade glioma planned for surgical resection as part of standard clinical care.
- Able to start disulfiram at least 3 days prior to planned surgery (treatment window 3-14 days pre-op).
- In-patient status for the duration of study.
- Karnofsky Performance Status (KPS) ≥70%.
Adequate organ function within 14 days prior to first dose:
- ANC ≥1.5 x 10^9/L
- Platelets ≥100 x 10^9/L
- Hemoglobin ≥9 g/dL
- AST/ALT ≤2.5 x ULN
- Total bilirubin ≤1.5 x ULN (unless Gilbert syndrome, in which case <5 x ULN).
- Total bilirubin ≤1.5 x ULN (unless Gilbert syndrome, in which case <5 x ULN).
- Ability to understand and willingness to sign written informed consent.
- Willingness to avoid alcohol and alcohol-containing products during treatment and for 14 days after last dose.
Exclusion Criteria:
- Any dexamethasone (or other systemic glucocorticoid for cerebral edema) administered prior to enrollment/first dose (including outpatient or ED administration). This does not include inhalers or topical steroids.
- Imaging features that are atypical for high-grade glioma that have reasonable concern for competing differential diagnoses (e.g. PCNSL, tumefactive MS, etc.)
- Known hypersensitivity to disulfiram or thiuram derivatives.
- Active or severe hepatic disease (e.g. hepatitis, cirrhosis, known liver disease that may be exacerbated by disulfiram), or baseline liver tests above inclusion thresholds.
- Current use of metronidazole or other contraindicated interacting medications. See section 6.0; medication reconciliation for the list of medications/foods.
- Pregnant or breastfeeding. Pregnant women are excluded from the trial because the safety in pregnancy has not been established. Women who are breastfeeding are excluded from the trial because it is not known if disulfiram is present in breast milk.
- Clinically unstable neurologic status requiring immediate steroid initiation, where delaying dexamethasone for a disulfiram trial would be unsafe (investigator judgment).
- Any condition that would limit compliance with alcohol avoidance or study procedures, or that would make participation unsafe in investigator judgment.
- Subjects receiving any other investigational agents.
- Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled or unstable cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Disulfiram
description here
|
250 milligrams (mg) disulfiram will be given daily for 3-14 prior to operation.
Participants can have the option to be treated at 500mg after initial evaluation.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Reduction in Complement Immunosuppressive program
Periodo de tiempo: day 0, up to 14 days
|
Evaluate whether disulfiram given pre-operation reduces the Complement Immunosuppressive myeloid program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
|
Reduction in Scavenger Immunosuppressive program
Periodo de tiempo: day 0, up to 14 days
|
Evaluate whether disulfiram given pre-operation reduces the Scavenger Immunosuppressive myeloid program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Proportion of participants needing dexamethasone within 48 hour window
Periodo de tiempo: 48 hours
|
Change in investigator-rated edema symptom composite score from baseline to Day 2 on therapy.
|
48 hours
|
|
Safety of disulfiram
Periodo de tiempo: 14 days
|
Safety is defined as the rates of adverse events experienced by participants.
Adverse event severity is graded according to the NCI Common Terminology for Adverse Events (CTCAE) Version 5.0
|
14 days
|
|
Change in Edema Symptom Composite Score (ESCS)
Periodo de tiempo: day 0, up to 14 days
|
Change in ESCS is analyzed using a Wilcoxon signed-rank test
|
day 0, up to 14 days
|
|
Tolerability of disulfiram
Periodo de tiempo: 14 days
|
Tolerability as measured by participant toxicity rates.
|
14 days
|
|
Change in Microglial Inflammatory program scores
Periodo de tiempo: day 0, up to 14 days
|
Evaluate the change in microglial inflammatory program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
|
Change in Systemic Inflammatory Program Scores
Periodo de tiempo: day 0, up to 14 days
|
Evaluate the change in systemic inflammatory program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Tiffany Hodges, MD, University Hospitals Cleveland Medical Center
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
Otros números de identificación del estudio
- CASE7326
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Marco de tiempo para compartir IPD
Criterios de acceso compartido de IPD
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
- CÓDIGO_ANALÍTICO
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.
producto fabricado y exportado desde los 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. .