Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain

• Register: ClinicalTrials.gov
• Last refreshed on: 12 December 2020
• Main ID: NCT03058965
• Date of registration: 12/01/2017
• Prospective Registration: No
• Primary sponsor: Molecular NeuroImaging
• Public title: Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain
• Scientific title: Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain of Patients With Probable Alzheimer's Disease or Progressive Supranuclear Palsy Compared With Healthy Volunteers
• Date of first enrolment: November 29, 2016
• Target sample size: 12
• Recruitment status: Completed
• URL: https://clinicaltrials.gov/show/NCT03058965
• Study type: Interventional
• Study design: Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Other. Masking: None (Open Label).
• Phase: Early Phase 1

Countries of recruitment

United States

Key inclusion & exclusion criteria

Inclusion:

- Written informed consent must be obtained before any assessment is performed.

- Female subjects must be documented by medical records or physician's note to 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 of child-bearing
potential, must commit to use 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.

- Male subjects must not donate sperm for the study duration.

- Willing and able to cooperate with study procedures

Inclusion Criteria for Healthy Volunteer Subjects:

- Males and females aged =50 years. Healthy with no clinically relevant finding on
physical examination at screening and upon reporting for the [18F]MNI-958 imaging
visit.

- No cognitive impairment from neuropsychological battery as judged by the investigator

- Have screening [18F]florbetapir PET imaging demonstrating no significant amyloid
binding based on qualitative analysis (visual read).

- No family history of Alzheimer's disease or neurological disease associated with
dementia

- Have a CDR score=0

Inclusion Criteria for subjects with a diagnosis of probable Alzheimer's disease (AD):

- Males and females aged 50 to 90 years.

- Have probable Alzheimer's disease, based on the NINCDS/ADRDA and DSM-IV criteria.

- Have a CDR score of 0.5 or greater at screening.

- Have an MMSE score = 28.

- Have screening or prior (in the last 12 months) [18F]florbetapir PET imaging
demonstrating amyloid binding based on qualitative (visual read)

- 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 30 days before the screening visit.

- Signed and dated written informed consent obtained from the subject and the subject's
legally authorized representative or caregiver (if applicable).

- The subject has an appropriate caregiver capable of accompanying subject, if
necessary.

Inclusion Criteria for subjects with a diagnosis of probable Progressive Suprnuclear Palsy
(PSP)

- Males and females aged 50 to 90 years.

- Has a clinical diagnosis of PSP based on the NINDS and Society for PSP criteria
(Litvan, et al 1996).

- Have screening or prior DaTscan SPECT imaging demonstrating evidence of dopamine
transporter deficit based on visual read.

- A brain MRI that supports a diagnosis of PSP, with no other evidence of significant
neurologic pathology

- Medications taken for symptomatic treatment of PSP must be maintained on a stable
dosage regimen for at least 30 days before screening visit.

- Signed and dated written informed consent obtained from the subject and the subject's
legally authorized representative or caregiver (if applicable).

- The subject has an appropriate caregiver capable of accompanying subject, if
necessary.

Exclusion Criteria:

- Current or prior history of any alcohol or drug abuse.

- Laboratory tests with clinically significant abnormalities and/or clinically
significant unstable medical illness.

- Subject has received an investigational drug or device within 30 days of screening

- Prior participation in other research protocols or clinical care in the last year in
addition to the radiation exposure expected from participation in this clinical study,
such that radiation exposure exceeds the effective dose of 50 mSv, which would be
above the acceptable annual limit established by the US Federal Guidelines

- Pregnancy, lactating 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: evidence of cerebrovascular disease (more than two
lacunar infarcts, any territorial infarct >1cm3, or deep white matter abnormality
corresponding to an overall Fazekas scale of 3 with at least one confluent
hyperintense lesion on the FLAIR sequence that is =20 mm in any dimension), 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 Probable AD:

- Has received treatment that targeted amyloid-ß or tau within the last 3 months.

Exclusion Criteria for Subjects with Probable PSP:

- Ongoing treatment with methylphenidate, bupropion, modafinil, metoclopramide, alpha
methyldopa, reserpine, or amphetamine derivative.



Age minimum: 50 Years
Age maximum: 90 Years
Gender: All

Health Condition(s) or Problem(s) studied

Healthy Volunteers

Progressive Supranuclear Palsy

Alzheimer Disease

Intervention(s)

Drug: [18F]MNI-958

Drug: DaTscan

Drug: [18F]Florbetapir

Primary Outcome(s)

Tracer uptake will be evaluated in regions of interest for analysis of regional [18F]MNI-958 binding/uptake and expressed in SUV by using established methods for normalization for 3 AD, 3 PSP, and 3 HV subjects. [Time Frame: 1 year]

Secondary ID(s)

[18F]MNI-958

Source(s) of Monetary Support

Please refer to primary and secondary sponsors