University of Kansas Medical Center

Condition

• Alzheimer Disease

Eligibility

Eligible Ages

Between 55 Years and 85 Years

Eligible Genders

All

Accepts Healthy Volunteers

No

Criteria

Inclusion

1. Written informed consent from the participant and legally acceptable representative
(trial partner).

2. Have a reliable and competent trial partner who must have a close relationship with
the participant, who has face to face contact at least three days a week for a minimum
of ten waking hours a week and is willing to accompany the participant to all trial
visits. The trial partner should understand the nature of the trial and adhere to
trial requirements (e.g., dose, visit schedules, receive phone calls, and
evaluations).

3. Male and female participants between the ages of 55 to 85 (inclusive).

4. If female, not be of childbearing potential as indicated by one of the following:

a. Has reached natural menopause defined as either: i. ≥ 12 months of spontaneous
amenorrhea or ii. ≥ 6 months of spontaneous amenorrhea with serum follicle stimulating
hormone (FSH) levels > 40 mIU/ml as determined by the central laboratory; b. Has had a
hysterectomy; or c. Has had a bilateral tubal ligation; or d. Has had a bilateral
oophorectomy (with or without a hysterectomy) and more than 6 weeks have passed since
the surgery.

5. If male, must agree to use a reliable method of birth control (condoms with
contraceptive forms or sexual abstinence) during the study and for 6 months after the
last dose of study drug.

6. Must fulfill one of the following:

1. A documented amyloid PET scan (florbetaben F18, florbetapir F18, or flutametamol
F18) determined as positive by the Investigator obtained at any time prior to the
Screening visit; or

2. A documented positive amyloid CSF result obtained at any time prior to the
Screening visit; or

3. Investigator has knowledge of positive amyloid PET scan or positive amyloid CSF
result obtained previously; or

4. A positive amyloid CSF result at screening. The cut-off value for CSF Aβ1-42 or
CSF Aβ1-42/Aβ1-40 ratio will be based on the value determined by Vaccinex

7. Evidence of cognitive impairment based on history and neuropsychological testing that
meet the diagnostic criteria for probable Alzheimer's dementia.

8. Global Clinical Dementia Rating (CDR) of 0.5 or 1.0

9. MMSE score of 17-26, inclusive.

10. Adequate vision, hearing, and motor function to comply with testing.

11. If receiving medications for AD (including but not limited to donepezil, rivastigmine,
galantamine, tacrine, and memantine), be on a stable dose for at least 8 weeks prior
to Screening Visit.

12. If on stable doses of centrally-acting medications, be on a stable dose for 8 weeks
prior to Screening Visit.

13. In the opinion of the Investigator, is in reasonably good health over the last 6
months and any chronic disease is stable based on medical history and screening
assessments.

Exclusion

1. Inability to comply with visit schedule or other protocol requirements.

2. Have participated in an investigational drug or device study within 30 days of the
Baseline Visit. If previous investigational drug was a monoclonal antibody,
antibody-drug conjugate, or similar protein therapeutic, 180 days or 5 half-lives,
whichever occurs first.

3. Have a known allergy to any ingredient in the study drug formulation.

4. Have a body weight greater than 125 kg.

5. Are a suicide risk, as determined by meeting any of the following criteria:

1. Suicide attempt within one year prior to the Baseline Visit.

2. Suicidal ideation as defined by a positive response to question 4 and 5 on the
C-SSRS within 60 days of the Baseline Visit.

6. Have a history of substance abuse (based on DSMIV criteria) within the past 12 months
prior to Screening.

7. Significant acute or chronic infection at Screening including, among others: Known
history of human immunodeficiency virus (HIV) or known acquired immunodeficiency
syndrome. Hepatitis B virus (HBV) or hepatitis C virus (HCV) infection (defined as,
HBV surface antigen positive or positive HCV antibody with reflex to positive HCV RNA)
at Screening.

8. Have clinically significant laboratory or ECG abnormalities at Screening in the
opinion of the Investigator.

9. Have clinically relevant hematologic, hepatic, cardiac, or renal disease.

10. Have a clinically significant medical, surgical, laboratory, or behavioral abnormality
which in the judgment of the Investigator makes the participant unsuitable for the
study, as well as anyone with a history of malignancy of any type within 2 years of
Screening. Persons with a history of surgically excised non-melanoma skin cancers,
superficial bladder or prostate cancer are permitted.

11. Participants who have a diagnosis of a neurological condition causing cognitive
impairment other than sporadic mild dementia due to AD (e.g., Lewy body disease or
frontotemporal dementia), a primary psychiatric diagnosis (e.g., Cognitive Impairment
due to Schizophrenia, CIAS), history of frequent concussions or significant findings
on brain MRI at screening inconsistent with AD (e.g., cerebrovascular disease or
tumor).

12. Have any of the following conditions (which would exclude MRI or PET participation):

1. Participants deemed unable to cooperate due to claustrophobia, inability to lie
on scanner bed for 45 minutes, or inability to achieve venous access sufficient
for tracer or pepinemab administration.

2. An implant/device/condition that is contraindicated for MRI (e.g., pacemaker,
severe claustrophobia, prosthetic heart valve, any metal fragments in the eyes or
body--in some cases, an X-ray may be needed before an MRI scan, to ensure it is
safe to enter the scanner).

3. Body habitus that would impede completion of imaging scans.

13. Has an MRI scan obtained at Screening that shows evidence of a neurological disorder
other than early AD or > 4 cerebral microhemorrhages (regardless of their anatomical
location or diagnostic characterization as "possible" or "definite"), a single area of
superficial siderosis,

14. Any other clinically significant finding on MRI (e.g., any lesion that may account for
their cognitive impairment, including but not limited to brain tumor, severe white
matter disease arteriovenous malformation, cavernous hemangioma, or any infarct in a
strategic cortical or subcortical location).

15. Are undergoing FDG-PET and have received research-related radiation exposure that
exceeds institutional guidelines in the prior year if applicable.

16. Are undergoing a LP for CSF collection and have any of the following conditions:
uncorrected bleeding or clotting disorders, skin infections near the site of the LP,
suspicion of increased intracranial pressure, allergies to numbing medications (local
anesthetics), acute spinal trauma.

17. Are undergoing a LP for CSF collection and taking any of the following types of
anticoagulants: coumarins and indandiones, Factor Xa inhibitors, heparins, or thrombin
inhibitors.

18. Has received treatment with any FDA accelerated approval therapy for treatment of
Alzheimer's Disease

19. Has a Screening MRI that shows Amyloid-related imaging abnormalities edema (ARIA-E)

Study Contact

Detailed Description

To investigate safety, tolerability, the effects on cognition and brain metabolism of pepinemab, administered as IV infusions every 4 weeks for 44 weeks (12 infusions) in mild dementia due to Alzheimer's Disease (AD)) participants. Participants will be randomized 1:1 to receive 40 mg/kg pepinemab or placebo. This is a randomized double-blind, placebo-controlled study of pepinemab in mild dementia due to AD. The study is 52 weeks in duration, including a safety and efficacy evaluation 4 weeks after the last dose of study drug. Participants with resolved adverse events at Week 48 will have a safety telephone call at Week 52. Participants with unresolved adverse events at Week 48 will have a safety in-office visit at Week 52. The study protocol will include two sentinel participants in each of the two blinded dose arms. Sentinel dosing will be implemented by randomly assigning one study participant to one of the two dose arms in a blinded manner, treating those participants with study drug. If no unexpected serious adverse events are observed within 48 hours after the first and second participants receive treatment, two additional participants will be enrolled, with one participant assigned randomly to each of the two dose arms. Again a 48-hour safety period will be observed following treatment of the fourth participant to document any unexpected safety events that may occur. Should no unexpected serious adverse events occur within 48 hours after the third and fourth participants receive treatment, the remaining participants will be assigned to the study dose arms according to the blinded randomization scheme and the 1:1 randomization ratio. Participants will be randomized to one of two treatment arms and will receive one dose of study drug every 4 weeks during the 44-week dosing period for a total of 12 doses of study drug. The primary objective is the safety and tolerability of study drug. A key secondary objective is the change in brain metabolism as assessed by [18F]fluorodeoxyglucose (FDG)-PET in the resting state.