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ReclutandoNCT07830771Registro de ClinicalTrials.gov

Fibroblast Activating Protein (FAP) PET/CT in Adults With Tuberculosis

Tuberculosis, Pulmonary

LO ESENCIAL

De qué trata este estudio

El registro indica que este estudio recluta participantes. La disponibilidad puede variar por centro.

Tipo de estudio
De intervención
Fase
Fase 1 temprana
Rango de edad
21 años - No especificado
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
10 Estimado

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

This is an early phase study in patients with Tuberculosis (TB) to evaluate Fibroblast Activating Protein (FAP) activation as a marker of fibrosis. The Investigators propose to use FAP PET/CT to define the extent and location of FAP signals in lungs of TB patients early in TB treatment and after TB cure. These timepoints are chosen as they could be utilized to deliver treatments designed to prevent, predict, or treat Post-transplant Lymphoproliferative Disorder (PTLD). The overarching hypothesis is that greater FAP signals in lungs of adult TB patients are associated with greater imaging manifestations of PTLD after cure.

Leer la descripción completa

Most participants will be receiving care at the clinical practices of the University of Pennsylvania or through City of Philadelphia TB Control Program (named the Flick clinic). Patients may participate in this study if they are at least 21 years of age and will be approached about study participation regardless of race or ethnic background. The study anticipates enrolling up to 10 participants who meet eligibility requirements for this study. Accrual is estimated to occur over approximately 2 years.

Investigators propose to use Fibroblast Activating Protein (FAP) PET/computed tomography (CT) to define the extent and location of FAP signals in lungs of TB patients at the time of TB treatment initiation and after TB cure. These timepoints are chosen as they could be utilized to deliver treatments designed to prevent, predict, or treat Post-transplant Lymphoproliferative Disorder (PTLD). The overarching hypothesis is that greater FAP signals in lungs of adult TB patients are associated with greater imaging manifestations of PTLD after cure. This is important, as radiographic findings in TB are associated with mortality.

This longitudinal study will perform FAP PET/CT and high-resolution CT (HRCT) within 6 weeks of TB treatment initiation and again within 6 months after TB cure to evaluate the hypothesis that change in total pulmonary FAP signal during treatment is associated with change in a measure of total lung structural damage previously validated in TB. It is expected that patients with less decrease in FAP lung signals will have less improvement in lung structural damage despite curative TB treatment.

After injection of \[F-18\]-FAPI-74, patients will undergo a vertex to mid-thigh scan, starting at approximately 30 minutes (± 5 min) post injection. PET/CT imaging sessions will include an injection of ≤ 8.0 mCi (expected range of doses is expected to be 6.0-8.0 mCi) of \[F-18\]-FAPI-74 intravenously. Data will be collected to evaluate uptake of \[F-18\]-FAPI-74 in the lung.

¿Quién podría participar?

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Inclusion Criteria

1. Participants will be ≥ 21 years of age
2. Diagnosed with microbiologically confirmed (culture or Xpert MTB/RIF PCR positive on at least one respiratory sample) pTB
3. Be currently on or able to initiate standard drug-sensitive pTB treatment according to IDSA guidelines.
4. Have initiated or planning to initiate TB treatment prior to screening and enrollment.
5. Have a Timika CXR score indicating cavitary disease
6. Be able and willing to provide written informed consent to participate in the study

Exclusion Criteria

1. Diagnosed with TB that is resistant to rifampin per medical record review or have only extrapulmonary TB.
2. Women of childbearing potential may not be pregnant or breast-feeding. A negative pregnancy test will be required before \[F-18\]-FAPI-74 injection.
3. Inability to tolerate imaging procedures in the opinion of an investigator or treating physician
4. Any current medical condition, illness, or disorder as assessed by medical record review and/or self-reported that is considered by a physician investigator to be a condition that could compromise participant safety or successful participation in the study, including completion of the study follow-up or TB treatment.
5. History of major alternative pulmonary disease such as asthma, chronic obstructive pulmonary disease (COPD), or interstitial lung disease as per medical record review or patient self-report. "Major" is defined as potentially resulting in pulmonary radiographic abnormalities that could interfere with interpretation of PET-CT scan data.
6. Have been administered at least 7 days of corticosteroids or any duration of another systemic investigational agent within 3 months of enrollment per medical record review or patient self-report
7. Have symptoms or signs that, in the opinion of the investigative team, are suggestive of active TB at the time of pre-screening per patient self-report

Entiende la evaluación inicial

Tratamiento, grupos y participación

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Asignación
No aplica
Enmascaramiento
Sin enmascaramiento
Pulmonary Tuberculosis Cohort

Participants aged 21 years of age or older with a diagnosis of pulmonary Tuberculosis

Drug: [18F]-FAPI-74

[18F]-FAPI-74 DRUG

Each patient will receive approximately 8 mCi of \[18F\]-FAPI-74 intravenously (approximate range for most studies is anticipated to be 6-8 mCi). This will be followed by a vertex to thigh static scan at 30 minutes ( ±5 min) post injection and a low dose CT for attenuation correction. Participants will also undergo high-resolution CT (HRCT) of the chest at baseline and follow-up timepoints, these scans may be done the same day or on different days.

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Determine the relationship between change in FAP PET signals in lungs during TB treatment and change in lung structural damage in adult patients treated for pulmonary TB.

Plazo: 6 months

Greater radiographic lung structural damage in TB, a hallmark of PTLD, is inversely associated with lung function and has repeatedly been associated with reduced survival in TB5, 21-23. This longitudinal study will perform FAP PET/CT and high-resolution CT (HRCT) within 6 weeks of TB treatment initiation and again within 6 months after TB cure to evaluate the hypothesis that change in total pulmonary FAP signal during treatment is associated with change in a measure of total lung structural damage previously validated in TB. It is expected that patients with less decrease in FAP lung signals will have less improvement in lung structural damage despite curative TB treatment.

Medidas secundarias

Characterize the association between FAP PET signals in lungs early after TB diagnosis and persistent lung structural damage after cure.

Plazo: 6 months

Investigators will use the longitudinal data from Aim 1 to evaluate the hypothesis that higher levels of total FAP signal in the lungs early will be associated with higher overall levels of residual structural lung damage on HRCT after TB cure. It is expected that higher baseline FAP signal will be associated with worse residual structural lung damage.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (1)

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1 centros

Perelman School of Medicine, Nuclear MedicinePhiladelphia, Pennsylvania, United StatesReclutando

Equipo y fechas

Patrocinador principal
University of Pennsylvania
Inicio del estudio
22 sept 2026 Real
Finalización primaria
30 sept 2028 Estimado
Finalización del estudio
30 sept 2030 Estimado
Primera publicación
21 sept 2026 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

Título oficial del estudio

Fibroblast Activating Protein (FAP) PET/CT in Adults With Tuberculosis

EL PRÓXIMO PASO, CON APOYO HUMANO

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 11 nov 2026 · Última actualización del registro: 10 nov 2026