Assessment of Foralumab Safety and Modulation of Microglial Activation Evaluated by PET Imaging in Patients With Early Symptomatic Alzheimer's Disease

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase 2a study will research the safety and tolerability of Foralumab, a human anti-CD3 antibody. An antibody is a molecule secreted by the immune system. These molecules are created to identify a specific pathogen. Previous data on experimental mice has suggested that Foralumab increases the immune system activity in the brain to reduce the inflammation of microglia, the brain's main immune cells. This combination of increased immune reactivity and less microglia inflammation may improve the immune response throughout the brain. Alzheimer's disease and other forms of dementia are characteristically known for the build-up of certain proteins in the brain. This trial will evaluate whether nasal Foralumab can improve cognition in participants with mild cognitive impairment due to early Alzheimer's or dementia. The trial will ask participants to administer Foralumab nasally three times a week for eight weeks. The administration will occur intermittently, with breaks between each dosing cycle. Participants will also receive brain scans (Amyloid PET and MRI), undergo cognitive testing, blood draws, and physical, neurological, and nasal exams. Volunteers are expected to remain in the trial for six months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 85
Healthy Volunteers: f
View:

• The Sponsor will rely on NIA-AA Alzheimer's Disease Diagnostic Guidelines for Early Symptomatic Alzheimer's Disease (AD) with a 20-30 MMSE score, Clinical Dementia Rating (CDR) global score of 0.5 or 1, and impaired memory performance below an education adjusted cut-off score on the Logical Memory II subscale delayed paragraph recall (LM-IIa) of the Wechsler Memory Scale- Revised (WMS-R) (127) (≥16 years: ≤8; 8-15 years: ≤4; 0-7 years: ≤2).

• Age between 60 and 85 years (inclusive).

• Good general health with no disease likely to interfere with the study assessments.

• On a stable medication regimen for eight weeks prior to the study and is anticipated to remain stable during the study.

• Subject is not pregnant, lactating, or of childbearing potential (i.e., women must be two years post-menopausal or surgically sterile). If a woman is of childbearing potential, her partner must use barrier contraception throughout the study.

• Amyloid-positive PET scan (performed only if the subject meets all other inclusion criteria). An amyloid-positive PET scan is classified by an SUVR composite score cutoff of 1.18 units. Prior evidence of amyloid positivity by PET or CSF will also be accepted for eligibility.

• Ability to understand and provide informed consent.

• Has availability of a study partner who has regular contact with the participant and knows him/her well.

Locations
United States
Massachusetts
Center for Alzheimer Research and Treatment, Brigham and Women's Hospital
RECRUITING
Boston
Contact Information
Primary
Gad Marshall, MD
foralumab@mgb.org
617-525-6754
Backup
Ryan de Lissovoy, BS
foralumab@mgb.org
617-278-0831
Time Frame
Start Date: 2025-09-16
Estimated Completion Date: 2026-12
Participants
Target number of participants: 16
Treatments
Active_comparator: Arm A: This cohort of subjects will receive 100µg/dosing day vs. placebo throughout the study.
This group will receive a nasal spray three times a week for two weeks, followed by a one-week rest. That cycle will occur three more times for a total of three months of drug intervention.
Active_comparator: Arm B: This cohort of subjects will receive 50µg/dosing day vs. placebo throughout the study.
This group will receive a nasal spray three times a week for two weeks, followed by a one-week rest. That cycle will occur three more times for a total of three months of drug intervention.
Related Therapeutic Areas
Sponsors
Leads: Brigham and Women's Hospital
Collaborators: Tiziana Life Sciences LTD

This content was sourced from clinicaltrials.gov