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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.

研究概览

地位

招聘中

研究类型

介入性

注册 (估计的)

20

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • Florida
      • Aventura、Florida、美国、33180
        • 招聘中
        • Visionary Investigator Network
      • Merritt Island、Florida、美国、32952
        • 尚未招聘
        • Meritt Island Research, LLC dba. Flourish Research
      • Miami、Florida、美国、33133
        • 招聘中
        • Visionary Investigator Network
      • Miami、Florida、美国、33176
        • 招聘中
        • Visionary Investigator Network
      • Winter Park、Florida、美国、32789
        • 招聘中
        • Clinical Site Partners, LLC dba Flourish Research
    • Georgia
      • Gainesville、Georgia、美国、30501
        • 招聘中
        • Center for Advanced Research & Education LLC dba Flourish Research Gainesville

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

50年 至 110年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
其他:GE-287 then Vizamyl

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

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

其他:VIZAMYL then GE-287

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

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

研究衡量的是什么?

主要结果指标

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

次要结果测量

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

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

合作者

调查人员

  • 研究主任:Paul Sherwin、GE Healthcare

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年9月30日

初级完成 (估计的)

2027年2月25日

研究完成 (估计的)

2027年2月25日

研究注册日期

首次提交

2026年9月21日

首先提交符合 QC 标准的

2026年10月7日

首次发布 (实际的)

2026年10月14日

研究记录更新

最后更新发布 (实际的)

2026年11月5日

上次提交的符合 QC 标准的更新

2026年11月4日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

There is not a plan to make IPD available.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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