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Flutemetamol F 18 Injection Formulation Comparison

2026年11月4日 更新者: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.

調査の概要

状態

募集

条件

介入・治療

研究の種類

介入

入学 (推定)

20

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Florida
      • Aventura、Florida、アメリカ、33180
        • 募集
        • Visionary Investigator Network
      • Merritt Island、Florida、アメリカ、32952
        • まだ募集していません
        • Meritt Island Research, LLC dba. Flourish Research
      • Miami、Florida、アメリカ、33133
        • 募集
        • Visionary Investigator Network
      • Miami、Florida、アメリカ、33176
        • 募集
        • Visionary Investigator Network
      • Winter Park、Florida、アメリカ、32789
        • 募集
        • Clinical Site Partners, LLC dba Flourish Research
    • Georgia
      • Gainesville、Georgia、アメリカ、30501
        • 募集
        • Center for Advanced Research & Education LLC dba Flourish Research Gainesville

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

50年~110年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:診断
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
他の:GE-287 then Vizamyl

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

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

他の:VIZAMYL then GE-287

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

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

この研究は何を測定していますか?

主要な結果の測定

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

二次結果の測定

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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

協力者

捜査官

  • スタディディレクター:Paul Sherwin、GE Healthcare

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年9月30日

一次修了 (推定)

2027年2月25日

研究の完了 (推定)

2027年2月25日

試験登録日

最初に提出

2026年9月21日

QC基準を満たした最初の提出物

2026年10月7日

最初の投稿 (実際)

2026年10月14日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月5日

QC基準を満たした最後の更新が送信されました

2026年11月4日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • GE-287-201

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

There is not a plan to make IPD available.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。