A Study of XPro1595 in Patients With Early Alzheimer's Disease With Biomarkers of Inflammation

Prior treatment

• Enrolled in another clinical trial where patients receive treatment with an investigational drug or treatment device or have had previous treatment with any investigational medicinal product within 60 days or 5 half-lives (whichever is longer) prior to study drug treatment;
• A prior organ or stem cell transplant;

Other illness

• Have any contraindications to MRI scanning, including cardiac pacemaker/defibrillator, ferromagnetic metal implants (e.g., in-skull and cardiac devices other than those approved as safe for use in MRI scanners);
• Lifetime history of a major psychiatric disorder including schizophrenia and bipolar disorder. Major depressive disorder that has resulted in 2 or more hospitalizations in a lifetime. Major depressive episode during the past 5 years that is judged by the clinical team unlikely to have been part of Alzheimer's prodrome. History of suicidality.
• History of substance abuse within 12 months; use of cannabis or cannabis products within 6 months of consent;

Other

• Patients will be excluded from the study if 1 or more of the following criteria are applicable:
• Receives considerable help to carry out basic ADL living either in the home or as a resident in a nursing home or similar facility;
• Seated blood pressure of ≥ 165/105 mmHg at Screening.

• To be eligible for study entry, patients must satisfy all of the following criteria:
• Adult patients 50 years to ≤ 85 years of age at the time of consent;
• Meets the diagnostic criteria of MCI of probable Alzheimer's disease (Jack et al. 2018; NIA-AA) or mild dementia as clinically described in McKhann, (2011) and corresponding to stages 3 or 4 of the revised AD staging system (Jack, 2018). (NIA-AA);
• Amyloid positive (documented in medical history or assessed during screening through blood test);
• Either currently or previously (in pre-AD condition) literate and capable of reading, writing, and communicating effectively with others;
• Residence in an assisted living is allowed as is personal assistances provided in the home, however at time of enrollment participant must be able to perform most ADL with minimal assistance, and participant must be permitted sufficient independence to allow assessment of change in ADL;
• Has a study partner for the duration of the trial who either lives in the same household or interacts with the patient at least 4 hours per day and on at least 4 days per week, who is knowledgeable about the patient's daytime and night-time behaviors and who can be available to attend all clinic visits in person at which caregiver assessments are performed.

Criteria the registry did not label

• The screening window for this trial is 45 days.