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Flutemetamol F 18 Injection Formulation Comparison

4 november 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Werving

Studietype

Ingrijpend

Inschrijving (Geschat)

20

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

    • Florida
      • Aventura, Florida, Verenigde Staten, 33180
        • Werving
        • Visionary Investigator Network
      • Merritt Island, Florida, Verenigde Staten, 32952
        • Nog niet aan het werven
        • Meritt Island Research, LLC dba. Flourish Research
      • Miami, Florida, Verenigde Staten, 33133
        • Werving
        • Visionary Investigator Network
      • Miami, Florida, Verenigde Staten, 33176
        • Werving
        • Visionary Investigator Network
      • Winter Park, Florida, Verenigde Staten, 32789
        • Werving
        • Clinical Site Partners, LLC dba Flourish Research
    • Georgia
      • Gainesville, Georgia, Verenigde Staten, 30501
        • Werving
        • Center for Advanced Research & Education LLC dba Flourish Research Gainesville

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

50 jaar tot 110 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Diagnostisch
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Ander: GE-287 then Vizamyl

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

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

Ander: VIZAMYL then GE-287

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

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

Wat meet het onderzoek?

Primaire uitkomstmaten

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

Secundaire uitkomstmaten

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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Medewerkers

Onderzoekers

  • Studie directeur: Paul Sherwin, GE Healthcare

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

30 september 2026

Primaire voltooiing (Geschat)

25 februari 2027

Studie voltooiing (Geschat)

25 februari 2027

Studieregistratiedata

Eerst ingediend

21 september 2026

Eerst ingediend dat voldeed aan de QC-criteria

7 oktober 2026

Eerst geplaatst (Werkelijk)

14 oktober 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

5 november 2026

Laatste update ingediend die voldeed aan QC-criteria

4 november 2026

Laatst geverifieerd

1 november 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

There is not a plan to make IPD available.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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