SEMA4D Blockade Safety and Brain Metabolic Activity in Alzheimer's Disease (AD)

Alzheimer Disease Clinical Trial

— SIGNAL-AD  

Official title:

SEMA4D Blockade Safety and Brain Metabolic Activity in Alzheimer's Disease (AD): A Multi-center, Randomized, Double-Blind, Placebo-Controlled Safety and Biomarker Study of Pepinemab Anti-SEMA4D Antibody in Early-AD

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04381468
• Other study ID #: VX15/2503-11
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• Start date: July 22, 2021
• Est. completion date: June 10, 2024

Study information

• Verified date: June 2023
• Source: Vaccinex Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate safety, tolerability, the effects on cognition and brain metabolism of pepinemab in early AD dementia (early AD) subjects.

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 50
• Est. completion date: June 10, 2024
• Est. primary completion date: June 5, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 55 Years to 85 Years

Eligibility

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 Aß1-42 or CSF Aß1-42/Aß1-40 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)

Related Conditions & MeSH terms

• Alzheimer Disease

Intervention

Drug:
• Pepinemab
Pepinemab is a humanized IgG4 monoclonal antibody. The antibody is formulated at 20 mg/mL in 20 mM Sodium Acetate buffer, pH 5.4, containing 130 mM Sodium Chloride and 0.02% Polysorbate 80
• Placebo
Placebo consists of formulation buffer only which is 20 mM Sodium Acetate buffer, pH 5.4, containing 130 mM Sodium Chloride and 0.02% Polysorbate 80

Locations

Country	Name	City	State
United States	Neurological Associates of Albany	Albany	New York
United States	Dent Neurological Associates	Amherst	New York
United States	Brain Matters Research	Delray Beach	Florida
United States	Re-Cognition Health	Fairfax	Virginia
United States	University of Kansas Medical Center	Fairway	Kansas
United States	Neuropsychiatric Research Center of Southwest Florida	Fort Myers	Florida
United States	Indiana University School of Medicine	Indianapolis	Indiana
United States	JEM Research Institute	Lake Worth	Florida
United States	Columbia University Irving Medical Center	New York	New York
United States	Premiere Research Institute of Palm Beach, Neurology	Palm Beach	Florida
United States	University of Rochester Medical Center	Rochester	New York
United States	Pacific Research Network, Inc	San Diego	California
United States	Brain Matters Research	Stuart	Florida
United States	Georgetown University	Washington	District of Columbia

Sponsors (3)

Lead Sponsor	Collaborator
Vaccinex Inc.	Alzheimer's Association, Alzheimer's Drug Discovery Foundation

Country where clinical trial is conducted

United States, 

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* Note: There are 32 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Peak serum concentration (Cmax)	PK parameter	Up to 36 weeks
Other	Area under the serum concentration vs. time curve (AUC)	PK parameter	Up to 36 weeks
Other	Half-life of pepinemab	PK parameter	Up to 36 weeks
Other	Serum and CSF levels of neuroinflammatory cytokines	IL-1, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12, IL13,IFN?, TNF-a, TGFß	Up to 36 weeks
Other	T- and B-Cell Quantitation by Flow Cytometry (TBNK)	B cells, total count; Natural killer (NK) cells, total count; T cells, total count; Absolute CD4/CD8 count with ratio	Up to 36 weeks
Other	Plasma and CSF concentration of neurofilament light chain (NfL)		Up to 36 weeks
Other	Plasma and CSF concentrations of Aß1-42/Aß1-40		Up to 36 weeks
Other	CSF levels of pepinemab		Up to 36 weeks
Other	CSF concentrations of tau and p-tau		Up to 36 weeks
Other	CSF concentrations of YKL-40		Up to 36 weeks
Other	Cellular SEMA4D levels	PD parameter to determine the level of SEMA4D expression on T lymphocytes	Up to 36 weeks
Other	Total soluble SEMA4D levels	PD parameter to determine levels of total soluble SEMA4D	Up to 36 weeks
Other	Effects on brain volume	As measured by MRI	Up to 36 weeks
Primary	Number of subjects with treatment emergent adverse events (TEAEs)	TEAEs are defined as Adverse events (AEs) with onset after date-time of first dose, or medical conditions present prior to the start of IP but increased in severity or relationship after date-time of first dose of IP.	Up to 40 weeks
Secondary	Effects on brain metabolism	As assessed by [18F]fluorodeoxyglucose (FDG)-PET in the resting state following administration of 20 mg/kg or 40 mg/kg pepinemab or placebo.	Up to 36 weeks
Secondary	Alzheimer's Disease Assessment Scale- Cognitive subscale (ADAS-cog13)	The Alzheimer's Disease Assessment Scale (ADAS-cog13) will be performed to test the cognition of subjects. The score ranges from 0 to 75,and higher values represent a better outcome.	Up to 36 weeks
Secondary	Clinical Dementia Rating (CDR)	The CDR assesses 3 domains of cognition (memory, orientation, judgment/problem solving) and 3 domains of function (community affairs, home/hobbies, personal care) using semi-structured interviews of both the study subject and an informant carried out by a trained rater. The CDR is scored using a standard methodology. Each domain is rated on a 5-point scale and lower numbers represent a better outcome.	Up to 36 weeks
Secondary	Mini Mental State Examination (MMSE)	Mini-Mental State Examination scores(MMSE) will be performed to test the cognition of subjects. The score ranges from 0 to 30,and higher values represent a better outcome.	Up to 36 weeks
Secondary	Alzheimer's Disease Cooperative Study - Activities of Daily Living	The ADCS-ADL assesses the competence of participants with AD in basic and instrumental activities of daily living (ADLs). It is administered by a clinician as a structured interview with a caregiver. The maximum score is 30. A higher score is better.	Up to 36 weeks
Secondary	Alzheimer's Disease Cooperative Study- Clinical Global Impression of Change (ADCS-CGIC)	The ADCS-CGIC focuses on clinicians' observations of change in the patient's cognitive, functional, and behavioral performance since the beginning of a trial. The ADCS-CGIC gives a discrete score that ranges from 1-7 with 7 being the worst outcome.	Up to 36 weeks
Secondary	Neuropsychiatric Inventory (NPI)	The NPI is a trial partner interview-based rating scale assessing 12 behavioral disturbances occurring in dementia subjects. Items are scored for both frequency and severity. Total scores range from 0-144 with higher scores indicating greater behavioral disturbances. For each item, the associated trial partner distress is also assessed.	Up to 36 weeks
Secondary	Immunogenicity of pepinemab in serum	As assessed by the frequency and titer of anti-drug antibodies.	Up to 36 weeks