A Study to Assess Hyperphosphorylated Tau PET Binding in Primary Progressive Aphasia

Overview

Información sobre este estudio

This study is designed to learn more about the use of a new imaging agent AV-1451 which shows strong binding to abmormal tau in the brain, to see if it will allow positron emission tomography (PET) scanning of tau in the brains of patients with Primary Progressive Aphasia.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

- Must be over the age of 18

- Must speak English as your primary language

- Must have an informant who can provide independent evaluation of functioning

- Must present with a chief complaint of progressive impairment of speech/language or
changes in behavior

- Must fulfill diagnostic criteria for Primary Progressive Aphasia or Frontotemporal
Dementia

Exclusion Criteria:

- Any subject who is mute or whose speech is unintelligible will be excluded

- All subjects with concurrent illnesses that could account for speech and language
deficits, such as traumatic brain injury, strokes or developmental syndromes, and
subjects meeting criteria for another neurodegenerative disease, such as amnestic
Alzheimer's type dementia, dementia with Lewy bodies, progressive supranuclear palsy,
and corticobasal syndrome will be excluded

- All pregnant, post-partum and breast-feeding women will be excluded

- Subjects will also be excluded if MRI is contraindicated (metal in head, cardiac pace
maker, etc.), if there is severe claustrophobia, if there are conditions that may
confound brain imaging studies (e.g. structural abnormalities, including subdural
hematoma or intracranial neoplasm), or if they are medically unstable or are on
medications that might affect brain structure or metabolism,(e.g. chemotherapy).

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 7/18/23. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Keith Josephs, M.D.

Abierto para la inscripción

Contact information:

Sarah Boland CCRP

(507)284-3863

Boland.Sarah@mayo.edu

More information

Publicaciones

Publications are currently not available
.
CLS-20204591

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