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- Ensayo clínico NCT07674693
Phase 1 Study of WBRT or PCSI With REYOBIQ for Leptomeningeal Metastases
A Phase 1 Study to Determine the Safety and Tolerability of Whole Brain Radiotherapy (WBRT) or Proton Craniospinal Irradiation (PCSI) With Multiple Doses of Rhenium-186 NanoLiposome (186RNL, REYOBIQ) Administered Via Intraventricular Catheter for Leptomeningeal Metastases
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Cancer Trials Inbox
- Correo electrónico: CancerTrials@nyulangone.org
Copia de seguridad de contactos de estudio
- Nombre: Jonathan Yang, MD, PhD
- Número de teléfono: 2127316030
- Correo electrónico: Jonathan.Yang@nyulangone.org
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- At least 18 years of age at screening
- Ability to understand the purposes and risks of the study and has signed a written informed consent document approved by the site-specific IRB
- Proven and documented LM evidenced by positive CSF cytology or CSF circulating tumor cells, from any primary solid tumor
- Patients may have received prior chemotherapy regimens and prior radiation (there is no limit)
- Karnofsky performance status of 60 to 100
Acceptable liver function:
- Bilirubin ≤ 1.5 times upper limit of normal
- AST (SGOT) and ALT (SGPT) ≤ 3.0 times upper limit of normal for subjects with normal liver
- AST (SGOT) and ALT (SGPT) ≤ 5.0 times upper limit of normal for subjects with liver metastasis
- Subjects with a creatinine clearance greater than or equal to 60 mL/min (using the Cockcroft-Gault Equation) for males and females.
Acceptable hematologic status (without hematologic support):
- ANC ≥ 1000 cells μL
- Platelet count ≥ 75,000/μL
- Hemoglobin ≥ 9.0 g/dL
- PT/INR and PTT ≤1.5 x ULN, unless treated with anticoagulants
- All women of childbearing potential must have a negative serum pregnancy test at screening. Male and female subjects must agree to use effective means of contraception (for example, surgical sterilization or the use of barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel or an IUD) with their partner from entry into the study through 6 months after the last dose.
Exclusion Criteria:
- The subject has not recovered to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE v6.0) Grade ≤ 1 from AEs due to antineoplastic agents, investigational drugs, or other medications that were administered prior to study. Prior AEs due to alopecia, anemia, and lymphopenia are not required to be recovered to Grade ≤ 1 prior to 186RNL treatment, assuming other inclusion criteria are satisfied.
- Ventriculo-peritoneal or ventriculo-atrial shunts or contraindications to placement of Ommaya reservoir.
- Females of childbearing potential who are pregnant, breast feeding, or may possibly be pregnant without a negative serum pregnancy test (see inclusion criteria).
- Serious intercurrent illness, clinically significant cardiac arrhythmias, uncontrolled systemic infection, symptomatic congestive heart failure or unstable angina pectoris within 3 months prior study drug, myocardial infarction, stroke, transient ischemic attack within 6 months, seizure disorder with any seizure occurring within 14 days prior to consenting or encephalopathy.
- Active severe non hematologic organ dysfunction such as renal, cardiac, hepatic, pulmonary, or gastrointestinal grade 3 or above.
- Toxicity from prior treatments (grade 3 or above) that have not subsided to grade 1.
- Patients with prior CNS directed EBRT.
- Cytotoxic systemic therapy is excluded if given within 14 days or 5 half-lives, whichever is shorter, prior to 186RNL treatment. Small-molecule kinase inhibitors, targeted therapies, immunotherapy, and hormonal therapy can be given up to the day of treatment per investigator discretion.
- Projected survival of less than 60 days.
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 |
|---|---|
|
Experimental: WBRT or PCSI followed by REYOBIQ
Patients will undergo WBRT or PCSI; following WBRT or PCSI, patients will initiate REYOBIQ in 28 (+/- 7 days) days following a dose escalation scheme.
|
Intraventricular injection via catheter. Patients will be assigned to three separate dosing schedules and once assigned they will remain on that dose level for up to 12 months (6 doses). Each dose will be 26.4 mCi, and participants will receive three doses for a total of 79.2 mCi. The time between doses will vary depending on the schedule (shown in table 1):
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Incidence of Dose-Limiting Toxicities (DLTs)
Periodo de tiempo: Up to Month 13 (28 Days Post-Final Dose)
|
The incidence of DLTs during the 28-day DLT window following any administration of REYOBIQ.
|
Up to Month 13 (28 Days Post-Final Dose)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Central Nervous System Progression-Free Survival (CNS PFS)
Periodo de tiempo: Up to Year 5
|
Defined as the time from first treatment to the date of leptomeningeal metastases (LM) progression or death from any cause, whichever occurs first.
|
Up to Year 5
|
|
Overall Survival (OS)
Periodo de tiempo: Up to Year 5
|
Defined as the time from first treatment to death from any cause.
|
Up to Year 5
|
|
Overall Response Rate (ORR)
Periodo de tiempo: Up to Year 5
|
Defined as the proportion of evaluable patients achieving a best overall response (complete or partial response) prior to progression.
|
Up to Year 5
|
|
Duration of Response (DoR)
Periodo de tiempo: Up to Year 5
|
Defined as the time from first treatment to the date of LM progression among responders.
|
Up to Year 5
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Jonathan Yang, MD, PhD, NYU Langone Health
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 25-01308
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
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.
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