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Flutemetamol F 18 Injection Formulation Comparison

4 de noviembre de 2026 actualizado por: GE Healthcare

A Multicenter, Phase 2, Open-Label, Randomized, Crossover Comparison of Two Formulations of Flutemetamol F 18 Injection

VIZAMYL (flutemetamol F 18 injection) is a drug used during Positron Emission Tomography (PET) brain scans. It helps doctors detect the presence of amyloid protein, which is associated with Alzheimer's disease and other conditions affecting memory or thinking. A new formulation of this drug, called GE-287, has been developed. This new formulation may offer advantages for patient tolerability and can be produced more reliably and efficiently.

The aim of the study is to determine whether the new formulation works as well as the current one in identifying amyloid in the brain, how it distributes in the body, and whether it is safe for use. The study will measure how much of the study drug goes to different organs (including the brain, heart, liver, and kidneys) and monitor for any side effects.

Descripción general del estudio

Estado

Reclutamiento

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

20

Fase

  • Fase 2

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

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Florida
      • Aventura, Florida, Estados Unidos, 33180
        • Reclutamiento
        • Visionary Investigator Network
      • Merritt Island, Florida, Estados Unidos, 32952
        • Aún no reclutando
        • Meritt Island Research, LLC dba. Flourish Research
      • Miami, Florida, Estados Unidos, 33133
        • Reclutamiento
        • Visionary Investigator Network
      • Miami, Florida, Estados Unidos, 33176
        • Reclutamiento
        • Visionary Investigator Network
      • Winter Park, Florida, Estados Unidos, 32789
        • Reclutamiento
        • Clinical Site Partners, LLC dba Flourish Research
    • Georgia
      • Gainesville, Georgia, Estados Unidos, 30501
        • Reclutamiento
        • Center for Advanced Research & Education LLC dba Flourish Research Gainesville

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

50 años a 110 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • The participant is at least 50 years of age

  • The participant (or a legally authorized representative of the participant) has read, signed, and dated an informed consent form (ICF) before any study procedures are performed.

  • The participant has been referred for PET imaging with VIZAMYL (flutemetamol F 18 injection) to estimate amyloid β neuritic plaque density for a) evaluation of suspected AD or other causes of cognitive decline and/or b) assessment of participant eligibility for amyloid β-directed therapy for MCI or mild AD as described in the prescribing information of the therapeutic products.

  • The participant is able and willing to comply with all study procedures, including lying supine and still in the PET scanner for at least 60 minutes (approximately 2.5 hours total per imaging session, including a break that will be approximately 30 minutes).

  • The participant is surgically sterile (has had documented bilateral oophorectomy, bilateral salpingectomy, hysterectomy, bilateral orchidectomy, and/or vasectomy with confirmation of success), postmenopausal (cessation of menses for more than 1 year), or:

    1. If the participant can become pregnant, the participant must:

      • use a highly effective method of contraception from Screening until 30 days after the last dose of flutemetamol F 18 injection,
      • have negative results for serum or urine human chorionic gonadotropin pregnancy tests performed at Screening and on the imaging days (with the result known before each administration), and
      • agree not to harvest or donate eggs until at least 30 days after the last dose of IMP.
    2. If the participant can impregnate another person and has a sexual partner who can become pregnant, the participant and partner must use adequate contraception from Screening until 90 days after the last dose of flutemetamol F 18 injection, and the participant must agree not to harvest or donate sperm from screening through 90 days after the last dose of flutemetamol F 18 injection. If the participant has a sexual partner who is already pregnant, both the participant and the partner must provide written informed consent, and both must agree to abstain from any form of sexual contact for at least 24 hours after flutemetamol F 18 injection administration, and both must agree that once sexual contact resumes, they will use condoms until at least 90 days after administration of the last dose of flutemetamol F 18 injection.

Exclusion Criteria:

  • The participant received or plans to receive another IMP within 30 days before signing informed consent until the end of participation in this study.
  • The participant has been treated with, or is being treated with, any medicinal product (drug, biologic, or device) believed to be disease-modifying with regard to MCI or AD (such as an anti-amyloid drug), or initiation of such a medical product cannot be postponed until the participant is no longer in this study.
  • Including participation in this study, the participant will have received >50 mSv total radiation exposure from medical procedures/tests in the past 12 months.
  • The participant has had a procedure (therapeutic or diagnostic) involving a radioisotope and it is not possible to wait at least 4 disintegration half-lives before PET imaging.
  • The participant has a measured or estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2 based on eligibility serum laboratory assessments.
  • The participant has a total bilirubin level >1.5X the upper limit of normal (ULN) and/or an aspartate transaminase (AST; serum glutamic-oxaloacetic transaminase [SGOT]) level >3X ULN, and/or an alanine transaminase (ALT, serum glutamic-pyruvic transaminase [SGPT]) level >3X ULN based on eligibility serum laboratory assessments.
  • Except for the participant's cognitive impairment, the participant has a history or current evidence of any condition, therapy, or other circumstance that might confound the results of the study, interfere with participation for the full duration of the study, or put the participant at undue risk as judged by the investigator, such that it is not in the best interest of the participant to participate in this study.
  • The participant has known/suspected structural abnormalities such as a space-occupying lesion or medical devices such as stents, coils, or electrodes in any key region that may interfere with PET imaging or interpretation/analysis of image data.
  • The participant is pregnant, planning to become pregnant, or lactating.
  • The participant has known or suspected diabetes.
  • The participant is not willing or able to fast completely (except for water and any required medications) for at least 6 hours before administration of IMP until after the post-dose blood samples have been collected on each imaging day.
  • The participant has known or suspected allergy or hypersensitivity to either IMP or any of their ingredients (including PS80).
  • The participant was previously enrolled in this study.

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: Diagnóstico
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Otro: GE-287 then Vizamyl

Drug: GE-287 185 MBq (±10%) of GE-287 administered intravenously

Drug: Vizamyl 185 MBq (±10%) of Vizamyl administered intravenously

Otro: VIZAMYL then GE-287

Drug: GE-287 185 MBq (±10%) of GE-287 administered intravenously

Drug: Vizamyl 185 MBq (±10%) of Vizamyl administered intravenously

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Comparison of Standard Uptake Value ratio in frontal and anterior cingulate brain region
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in posterior cingulate and precuneus brain region
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in lateral temporal brain region
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in inferolateral parietal brain region
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of Standard Uptake Value (SUV) in heart
Periodo de tiempo: 0-60 minutes after product administration
0-60 minutes after product administration
Comparison of SUV in liver
Periodo de tiempo: 0-60 minutes after product administration
0-60 minutes after product administration
Comparison of SUV in kidneys
Periodo de tiempo: 0-60 minutes after product administration
0-60 minutes after product administration

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Comparison of global brain Centiloid values
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUV in heart
Periodo de tiempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of SUV in liver
Periodo de tiempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of SUV in kidneys
Periodo de tiempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of blinded visual image interpretations without quantification
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of blinded visual image interpretations with quantification
Periodo de tiempo: Time Frame: 90-100 minutes after product administration
Time Frame: 90-100 minutes after product administration
Comparison of inter-reader agreement of the blinded visual image interpretations without quantification
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of inter-reader agreement of the blinded visual image interpretations with quantification
Periodo de tiempo: 90-100 minutes after product administration
90-100 minutes after product administration
Safety: Treatment-emergent adverse event [TEAE] incidence
Periodo de tiempo: From pre-administration through 24 hours after product administration
From pre-administration through 24 hours after product administration
Safety: Changes from baseline in blood hematology
Periodo de tiempo: From pre-administration through 180 minutes after product administration
From pre-administration through 180 minutes after product administration
Safety: Change from baseline in serum biochemistry
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in urinalysis
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in blood pressure
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in heart rate
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in respiratory rate
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in temperature
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in general appearance, rated as normal or abnormal by a qualified healthcare provider.
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in examination of the heart, rated as normal or abnormal by a qualified healthcare provider.
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in examination of the lungs, rated as normal or abnormal by a qualified healthcare provider.
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiograms [ECGs] heart rate
Periodo de tiempo: from pre-administration through 180 minutes after product administration.
from pre-administration through 180 minutes after product administration.
Safety: changes from baseline in 12-lead electrocardiogram [ECG] heart rhythm
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] RR interval
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] PR interval
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] QRS interval
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] QT interval
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] QTc interval
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in 12-lead electrocardiogram [ECG] notation of abnormalities
Periodo de tiempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration

Colaboradores e Investigadores

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

Patrocinador

Colaboradores

Investigadores

  • Director de estudio: Paul Sherwin, GE Healthcare

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 (Actual)

30 de septiembre de 2026

Finalización primaria (Estimado)

25 de febrero de 2027

Finalización del estudio (Estimado)

25 de febrero de 2027

Fechas de registro del estudio

Enviado por primera vez

21 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de octubre de 2026

Publicado por primera vez (Actual)

14 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de noviembre de 2026

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

4 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

There is not a plan to make IPD available.

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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