Evaluation of [18F] PBR111 and PET as a Marker of Inflammation in Subjects With Neurological Conditions

This is a phase 1, open-label, single-center, non-randomized single dose study to assess the
kinetics, clearance and cerebral distribution of PBR-111 positron emission tomography (PET)
imaging in detecting microglial activation in the brain in patients with probable Alzheimer
disease (AD) compared to healthy volunteers (HVs). All aspects related to image
acquisition, processing and visual as well as quantitative evaluation will be developed,
optimized and validated (where required).

Each subject will be required to visit the study center during the screening phase and on
the PBR-111 PET imaging day (baseline). A telephone follow-up visit will be performed 7
days (+/- 3 days) after PBR-111 PET administration.

At the screening visit, each subject (or caregiver in the case of AD subjects) will be asked
to provide written informed consent or assent. During the screening phase (maximum duration
- 60 days) subject medical, neurological and surgical history, clinical assessments and a
neuro-psychiatric evaluation will be performed on all eligible subjects. Subjects will be
allowed to leave the center after all evaluations have been completed. During this period
an MRI of the brain will be performed. During the PBR-111 PET imaging day, all subjects
will receive a single IV injection of PBR-111 and scanning will be performed over a 3.5 hour
period. Each subject will have a telephone follow-up 7 days (+/- 3 days) thereafter to
assess for adverse events.

INCLUSION CRITERIA: Alzheimer Disease (AD)

1. The participant is 50 years or older.

2. Written informed consent is obtained.

3. Participants have a clinical diagnosis of probable Alzheimer disease based on
National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer
Disease and Related Disorders Association (NINCDS/ADRDA) criteria.

4. Does not fulfill the ICC criteria for probable DLB (Appendix 3), the NINDS-AIREN for
probable Vascular dementia (Appendix 5), or the Neary [Neary et al. 1998] criteria
for FTD (Appendix 4)

5. Clinical Dementia Rating Scale score ≤ 2.

6. Modified Hachinski Ischemia Scale score of ≤ 4.

7. MRI brain scan findings that do not reveal changes indicative of stroke and/or
generalized cerebrovascular disease (e.g., the ARWMC scale) changes limited to: a
white matter lesion score of 0 or 1 or 2 and a basal ganglia score of 0 or 1)

8. has a caregiver willing and able to attend all study visits and perform the
psychometric tests requiring the presence of a caregiver

9. For females, non-child bearing potential or a negative urine or blood pregnancy test
on day of [18F]-PBR111 injection.

EXCLUSION CRITERIA: Alzheimer Disease (AD)

1. History of significant cerebrovascular disease.

2. Clinically significant abnormal laboratory value and/or clinically significant
unstable medical or psychiatric illness

3. Evidence of clinically significant gastrointestinal, cardiovascular, hepatic, renal,
hematological, neoplastic, endocrine, neurological, immunodeficiency, pulmonary, or
other disorder or disease.

4. Pregnancy

5. Contraindication to MRI examination, e.g. metal implants or phobia as determined by
the onsite radiologist performing the scan

6. History of exposure to any radiation >15 mSv/year (e.g. occupational or radiation
therapy)

7. Receiving drug therapy or other treatment that is known to lead to greatly
fluctuating values of the hematological or chemical laboratory parameters or to
severe side effects (e.g. chemotherapy)

8. Received anti-amyloid drug therapy.

INCLUSION CRITERIA: Healthy Volunteer (HV)

1. The participant is 18 years or older, with at least 4 subjects ≥50 years.

2. Written informed consent is obtained.

3. Negative history of neurological or psychiatric illness based on evaluation by a
research physician.

4. Has no evidence of cognitive impairment as indicated by a clinical dementia rating
(CDR, [Hughes et al. 1993]) score of 0 (zero) and a score of ≥ 28 in the Mini-Mental
Status Examination (MMSE, [Folstein et al. 1975]) Clinical Dementia Rating score = 0.

5. has MRI brain scan that has been judged as "normal (age- appropriate)" including
ARWMC scale [Wahlund et al. 2001] scores supporting the lack of cerebrovascular
disease (e.g., a white matter lesion score of 0 or 1 or 2 and a basal ganglia score
of 0 or 1) and a Scheltens scale [Scheltens et al. 1992] verifying the lack of
cerebral atrophy (e.g. bilateral temporal lobe atrophy visual score of 0 or 1)

6. For females, non-child bearing potential a negative urine or blood pregnancy test on
day of [18F]-PBR-111 injection.

EXCLUSION CRITERIA: Healthy Volunteer (HV)

1. History of significant cerebrovascular disease.

2. Clinically significant abnormal laboratory value and/or clinically significant
unstable medical or psychiatric illness

3. Evidence of clinically significant gastrointestinal, cardiovascular, hepatic, renal,
hematological, neoplastic, endocrine, neurological, immunodeficiency, pulmonary, or
other disorder or disease.

4. Pregnancy

5. Contraindication to MRI examination, e.g. metal implants or phobia as determined by
the on-site radiologist performing the scan

6. History of exposure to any radiation >15 mSv/year (e.g. occupational or radiation
therapy)

7. Receiving drug therapy or other treatment that is known to lead to greatly
fluctuating values of the hematological or chemical laboratory parameters or to
severe side effects (e.g. chemotherapy)