- ICH GCP
- USA klinikai vizsgálatok nyilvántartása
- Klinikai vizsgálat NCT07873463
Flutemetamol F 18 Injection Formulation Comparison
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.
A tanulmány áttekintése
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 2. fázis
Kapcsolatok és helyek
Tanulmányi kapcsolat
- Név: Paul Sherwin
- Telefonszám: +1 (609) 5103686
- E-mail: PaulSherwin@gehealthcare.com
Tanulmányozza a kapcsolattartók biztonsági mentését
- Név: Victoria Haas
- Telefonszám: 011 33 6 29 86 53 56
- E-mail: ge287201@gehealthcare.com
Tanulmányi helyek
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Florida
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Aventura, Florida, Egyesült Államok, 33180
- Toborzás
- Visionary Investigator Network
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Merritt Island, Florida, Egyesült Államok, 32952
- Még nincs toborzás
- Meritt Island Research, LLC dba. Flourish Research
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Miami, Florida, Egyesült Államok, 33133
- Toborzás
- Visionary Investigator Network
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Miami, Florida, Egyesült Államok, 33176
- Toborzás
- Visionary Investigator Network
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Winter Park, Florida, Egyesült Államok, 32789
- Toborzás
- Clinical Site Partners, LLC dba Flourish Research
-
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Georgia
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Gainesville, Georgia, Egyesült Államok, 30501
- Toborzás
- Center for Advanced Research & Education LLC dba Flourish Research Gainesville
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-
Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
Egészséges önkénteseket fogad
Tanulmányozható nemek
Leírás
Inclusion Criteria:
-
The participant is at least 50 years of age
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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.
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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.
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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).
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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:
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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.
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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.
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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.
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Diagnosztikai
- Kiosztás: Véletlenszerűsített
- Beavatkozó modell: Crossover kiosztás
- Maszkolás: Egyetlen
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
|---|---|
|
Egyéb: GE-287 then Vizamyl
|
Drug: GE-287 185 MBq (±10%) of GE-287 administered intravenously Drug: Vizamyl 185 MBq (±10%) of Vizamyl administered intravenously |
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Egyéb: VIZAMYL then GE-287
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Drug: GE-287 185 MBq (±10%) of GE-287 administered intravenously Drug: Vizamyl 185 MBq (±10%) of Vizamyl administered intravenously |
Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Időkeret |
|---|---|
|
Comparison of Standard Uptake Value ratio in frontal and anterior cingulate brain region
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of SUVr in posterior cingulate and precuneus brain region
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of SUVr in lateral temporal brain region
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of SUVr in inferolateral parietal brain region
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of Standard Uptake Value (SUV) in heart
Időkeret: 0-60 minutes after product administration
|
0-60 minutes after product administration
|
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Comparison of SUV in liver
Időkeret: 0-60 minutes after product administration
|
0-60 minutes after product administration
|
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Comparison of SUV in kidneys
Időkeret: 0-60 minutes after product administration
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0-60 minutes after product administration
|
Másodlagos eredményintézkedések
Eredménymérő |
Időkeret |
|---|---|
|
Comparison of global brain Centiloid values
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
|
Comparison of SUV in heart
Időkeret: 105-150 minutes after product administration
|
105-150 minutes after product administration
|
|
Comparison of SUV in liver
Időkeret: 105-150 minutes after product administration
|
105-150 minutes after product administration
|
|
Comparison of SUV in kidneys
Időkeret: 105-150 minutes after product administration
|
105-150 minutes after product administration
|
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Comparison of blinded visual image interpretations without quantification
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of blinded visual image interpretations with quantification
Időkeret: Time Frame: 90-100 minutes after product administration
|
Time Frame: 90-100 minutes after product administration
|
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Comparison of inter-reader agreement of the blinded visual image interpretations without quantification
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
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Comparison of inter-reader agreement of the blinded visual image interpretations with quantification
Időkeret: 90-100 minutes after product administration
|
90-100 minutes after product administration
|
|
Safety: Treatment-emergent adverse event [TEAE] incidence
Időkeret: From pre-administration through 24 hours after product administration
|
From pre-administration through 24 hours after product administration
|
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Safety: Changes from baseline in blood hematology
Időkeret: From pre-administration through 180 minutes after product administration
|
From pre-administration through 180 minutes after product administration
|
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Safety: Change from baseline in serum biochemistry
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
|
Safety: changes from baseline in urinalysis
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in temperature
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in general appearance, rated as normal or abnormal by a qualified healthcare provider.
Időkeret: from pre-administration through 180 minutes after product administration
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from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in examination of the heart, rated as normal or abnormal by a qualified healthcare provider.
Időkeret: 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.
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiograms [ECGs] heart rate
Időkeret: from pre-administration through 180 minutes after product administration.
|
from pre-administration through 180 minutes after product administration.
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] heart rhythm
Időkeret: from pre-administration through 180 minutes after product administration
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from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] RR interval
Időkeret: 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
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] QRS interval
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] QT interval
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] QTc interval
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
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Safety: changes from baseline in 12-lead electrocardiogram [ECG] notation of abnormalities
Időkeret: from pre-administration through 180 minutes after product administration
|
from pre-administration through 180 minutes after product administration
|
Együttműködők és nyomozók
Szponzor
Együttműködők
Nyomozók
- Tanulmányi igazgató: Paul Sherwin, GE Healthcare
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Tényleges)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
Kulcsszavak
További vonatkozó MeSH feltételek
Egyéb vizsgálati azonosító számok
- GE-287-201
Terv az egyéni résztvevői adatokhoz (IPD)
Tervezi megosztani az egyéni résztvevői adatokat (IPD)?
IPD terv leírása
There is not a plan to make IPD available.
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