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Flutemetamol F 18 Injection Formulation Comparison

4 novembre 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

20

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Florida
      • Aventura, Florida, Stati Uniti, 33180
        • Reclutamento
        • Visionary Investigator Network
      • Merritt Island, Florida, Stati Uniti, 32952
        • Non ancora reclutamento
        • Meritt Island Research, LLC dba. Flourish Research
      • Miami, Florida, Stati Uniti, 33133
        • Reclutamento
        • Visionary Investigator Network
      • Miami, Florida, Stati Uniti, 33176
        • Reclutamento
        • Visionary Investigator Network
      • Winter Park, Florida, Stati Uniti, 32789
        • Reclutamento
        • Clinical Site Partners, LLC dba Flourish Research
    • Georgia
      • Gainesville, Georgia, Stati Uniti, 30501
        • Reclutamento
        • Center for Advanced Research & Education LLC dba Flourish Research Gainesville

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 50 anni a 110 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Diagnostico
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Altro: GE-287 then Vizamyl

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

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

Altro: VIZAMYL then GE-287

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

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

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Comparison of Standard Uptake Value ratio in frontal and anterior cingulate brain region
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in posterior cingulate and precuneus brain region
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in lateral temporal brain region
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUVr in inferolateral parietal brain region
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of Standard Uptake Value (SUV) in heart
Lasso di tempo: 0-60 minutes after product administration
0-60 minutes after product administration
Comparison of SUV in liver
Lasso di tempo: 0-60 minutes after product administration
0-60 minutes after product administration
Comparison of SUV in kidneys
Lasso di tempo: 0-60 minutes after product administration
0-60 minutes after product administration

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Comparison of global brain Centiloid values
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of SUV in heart
Lasso di tempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of SUV in liver
Lasso di tempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of SUV in kidneys
Lasso di tempo: 105-150 minutes after product administration
105-150 minutes after product administration
Comparison of blinded visual image interpretations without quantification
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Comparison of blinded visual image interpretations with quantification
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 90-100 minutes after product administration
90-100 minutes after product administration
Safety: Treatment-emergent adverse event [TEAE] incidence
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in urinalysis
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration
Safety: changes from baseline in temperature
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: from pre-administration through 180 minutes after product administration
from pre-administration through 180 minutes after product administration

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Investigatori

  • Direttore dello studio: Paul Sherwin, GE Healthcare

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

30 settembre 2026

Completamento primario (Stimato)

25 febbraio 2027

Completamento dello studio (Stimato)

25 febbraio 2027

Date di iscrizione allo studio

Primo inviato

21 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

7 ottobre 2026

Primo Inserito (Effettivo)

14 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

4 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • GE-287-201

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

There is not a plan to make IPD available.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .