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CompletedNCT02531360Updated Dec 16, 2016

Evaluation of [18F]MNI-815 as a Potential PET Radioligand for Imaging Tau Protein in the Brain of Patients With Tauopathies

An Early Phase 1 interventional study of [18F]MNI-815 (MNI-815) in Alzheimer's Disease (AD), Progressive Supranuclear Palsy (PSP) and Cortical Basal Syndrome (CBS), sponsored by Molecular NeuroImaging. Completed at 1 site in United States. Open to participants aged 50 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-12-16.

Sponsored by Molecular NeuroImaging · Early Phase 1 and Interventional

Phase
Early Phase 1
Study type
Interventional
Enrollment
7
Allocation
Not applicable
Ages
50 Years to 90 Years
Sex
All
01

Study summary

The overall goal of this imaging trial is to characterize [18F]MNI-815, a PET radioligand for imaging Tau.

02

Conditions studied

  • Alzheimer's Disease (AD)
  • Progressive Supranuclear Palsy (PSP)
  • Cortical Basal Syndrome (CBS)
  • Frontal Temporal Dementia (FTD)
03

Who can participate

Ages eligible
50 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

For all subjects:

  • Written informed consent must be obtained before any assessment is performed.
  • Female subjects must be either surgically sterile (by means of hysterectomy, bilateral oophorectomy, or tubal ligation) or post-menopausal for at least 1 year or, if they are child-bearing potential, must commit to use of a barrier contraception method for the duration of the study.
  • Male subjects and their partners of childbearing potential must commit to the use of two methods of contraception, one of which is a barrier method for male subjects for the study duration
  • Willing and able to cooperate with study procedures

Healthy Control subjects:

  • Males and females aged between 50 - 70 years. Healthy with no clinically relevant finding on physical examination at screening and upon reporting for the [18F]MNI-815 imaging visit.
  • No cognitive impairment from neuropsychological battery as judged by the investigator
  • Have a CDR score=0
  • Has FBB PET imaging demonstrating no evidence for significant amyloid binding based on qualitative (visual read) and quantitative analysis.
  • Modified Hachinski Ischemia Scale score of ≤ 4.

Prodromal or Moderate Alzheimer's Disease subjects:

  • Males and females aged between 50 - 90 years.
  • Have prodromal or moderate Alzheimer's disease, based on the NINCDS/ADRDA and DSM-IV criteria.
  • Have a CDR score of 0.5 for prodromal AD subjects and CDR > 1.0 for moderate AD subject at screening.
  • Has a FBB PET imaging demonstrating amyloid binding based on qualitative (visual read) and quantitative analysis.
  • Modified Hachinski Ischemia Scale score of ≤ 4.
  • A brain MRI that supports a diagnosis of AD, with no evidence of focal disease to account for dementia or MRI exclusion criteria.
  • Medications taken for symptomatic treatment of AD must be maintained on a stable dosage regimen for at least 1 month before the [18F]MNI-815 imaging visit.
  • The subject has an appropriate caregiver capable of accompanying subject on all visits.
  • Signed and dated written informed consent obtained from the subject and, when applicable, the subject's legally authorized representative or caregiver.

Frontotemporal Dementia subjects:

  • Has a clinical diagnosis of FTD based on consensus for clinical diagnosis of frontotemporal dementia criteria (Neary, et al 1998)
  • Has a FBB PET imaging demonstrating no evidence of significant amyloid binding based on qualitative (visual read) and quantitative analysis.
  • A brain MRI that supports a diagnosis of FTD, with no evidence of focal disease to account for dementia or MRI exclusion criteria.
  • Medications taken for symptomatic treatment of cognitive dysfunction must be maintained on a stable dosage regimen for at least 1 month before the screening visit.
  • The subject has an appropriate caregiver capable of accompanying subject on all visits to the center.
  • Signed and dated written informed consent obtained from the subject and, when applicable, the subject's legally authorized representative or caregiver.
  • Modified Hachinski Ischemia Scale score of ≤ 4.

Progressive Supranuclear Palsy subjects:

  • Has a clinical diagnosis of PSP based the NINDS and Society for PSP criteria (Litvan, et al 1996)
  • Has FBB PET imaging demonstrating no evidence of significant amyloid binding based on qualitative (visual read) and quantitative analysis.
  • A brain MRI that supports a diagnosis of PSP, with no evidence of focal disease to account for dementia or MRI exclusion criteria.
  • Medications taken for treatment of PSP symptoms must be maintained on a stable dosage regimen for at least 1 month before the screening visit.
  • The subject has an appropriate caregiver capable of accompanying subject on all visits to the center.
  • Signed and dated written informed consent obtained from the subject and, when applicable the subject's legally authorized representative or caregiver.
  • Modified Hachinski Ischemia Scale score of ≤ 4.

Corticobasal Syndrome Subjects:

  • Has a clinical diagnosis of CBS based on consensus criteria for possible or probable corticobasal degeneration (Armstrong et al, 2013)
  • Has a FBB PET imaging demonstrating no evidence of significant amyloid binding based on qualitative (visual read) and quantitative analysis.
  • A brain MRI that supports a diagnosis of CBS, with no evidence of focal disease to account for dementia or MRI exclusion criteria.
  • Medications taken for treatment of CBS symptoms must be maintained on a stable dosage regimen for at least 1 month before the screening visit.
  • The subject has an appropriate caregiver capable of accompanying subject on all visits to the center.
  • Signed and dated written informed consent obtained from the subject and, when applicable, the subject's legally authorized representative or caregiver.
  • Modified Hachinski Ischemia Scale score of ≤ 4.

Exclusion Criteria:

For all subjects

  • Current or prior history of any alcohol or drug abuse.
  • Laboratory tests with clinically significant abnormalities and/or clinically significant unstable medical illness.
  • Prior participation in other research protocols or clinical care in the last year such that radiation exposure is >15 mSv and would exceed the annual limits.
  • Pregnancy or breastfeeding.
  • Evidence of clinically significant gastrointestinal, cardiovascular, hepatic, renal, hematological, neoplastic, endocrine, alternative neurological, immunodeficiency, pulmonary, or other disorder or disease.
  • Unsuitable veins for repeated venipuncture.
  • MRI exclusion criteria include: Pathology that may be responsible for the neurologic status of the patient such as infectious disease, space-occupying lesions, normal pressure hydrocephalus or any other abnormalities associated with CNS disease,
  • Implants such as implanted cardiac pacemakers or defibrillators, insulin pumps, cochlear implants, metallic ocular foreign body, implanted neural stimulators, CNS aneurysm clips and other medical implants that have not been certified for MRI, or history of claustrophobia in MRI.

Exclusion criteria for subjects with AD subjects:

  • Has received treatment that targeted amyloid-beta or tau within the last 24 months.
  • Has a FBB PET imaging demonstrating no evidence of significant amyloid binding irrespective of other previous measurements of beta amyloid that may be available for review.

Exclusion criteria for subjects with PSP or CBS subjects:

  • Has FBB PET imaging with evidence of significant amyloid binding irrespective of other previous measurements of beta amyloid that may be available for review.
  • Has received treatment that targeted tau within the last 24 months.
  • Have any other neurological condition other than CBS or PSP that could account for cognitive or motor deficits including: Specifically:
  • A diagnosis of idiopathic Parkinson's disease or Lewy body dementia and/or have a prominent and sustained response to levodopa therapy;
  • History of repeated strokes with stepwise progression of parkinsonian features or history of major stroke

FTD subjects:

  • Has FBB PET imaging with evidence of significant amyloid binding irrespective of other previous measurements of beta amyloid that may be available for review.
  • Has received treatment that targeted tau within the last 24 months.

Healthy subjects:

•Has FBB PET imaging with evidence of significant amyloid binding irrespective of other previous measurements of beta amyloid that may be available for review.

04

Study design

Phase
Early Phase 1
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
7 participants (actual)

Study arms

  • Experimental
    [18F]MNI-815 (MNI-815)

    At the \[18F\]MNI-815 PET imaging visit, subjects will be injected with no more than 10mCi of \[18F\]MNI-815

    Drug: [18F]MNI-815 (MNI-815)

Interventions

  • Drug[18F]MNI-815 (MNI-815)

    All enrolled subjects will undergo an \[18F\]MNI-815 PET imaging visit. As a part of the screening visit, subjects will undergo \[18F\]florbetaben (FBB) PET imaging to determine if they have significant amyloid deposition.

    Also known as: [18F]MNI-815, FBB, [18F]Florbetaben

05

What researchers measure

Primary outcomes

  1. Brain uptake of [18F]MNI-815

    The PET imaging outcome measure to evaluate tau burden will be the standardized uptake value (SUV), which will be calculated for the areas of interest by using the established methods for normalizing to subject weight and injected dose.

    Time frame: 18 months

06

Study locations

1 site
  • Molecular NeuroImaging, LLC
    New Haven, Connecticut 06510, United States
07

References and documents

Publications

  • Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, Freedman M, Kertesz A, Robert PH, Albert M, Boone K, Miller BL, Cummings J, Benson DF. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology. 1998 Dec;51(6):1546-54. doi: 10.1212/wnl.51.6.1546. PubMed 9855500 ↗
  • Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin RC, Goetz CG, Golbe LI, Grafman J, Growdon JH, Hallett M, Jankovic J, Quinn NP, Tolosa E, Zee DS. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology. 1996 Jul;47(1):1-9. doi: 10.1212/wnl.47.1.1. PubMed 8710059 ↗
  • Armstrong MJ, Litvan I, Lang AE, Bak TH, Bhatia KP, Borroni B, Boxer AL, Dickson DW, Grossman M, Hallett M, Josephs KA, Kertesz A, Lee SE, Miller BL, Reich SG, Riley DE, Tolosa E, Troster AI, Vidailhet M, Weiner WJ. Criteria for the diagnosis of corticobasal degeneration. Neurology. 2013 Jan 29;80(5):496-503. doi: 10.1212/WNL.0b013e31827f0fd1. PubMed 23359374 ↗
08

Registry details

Key details

Study ID
NCT02531360
Lead sponsor
Molecular NeuroImaging
Collaborators
Life Molecular Imaging SA
Responsible party
Danna Jennings (Principal Investigator, Molecular NeuroImaging) — Principal investigator
First posted
Aug 24, 2015
Start date
May 2015
Primary completion
Jul 2016
Completion
Aug 2016
Last update
Dec 16, 2016

Study contacts

Danna Jennings, MD
principal investigator · Molecular NeuroImaging, LLC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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