Overview

A Study of Different Donanemab (LY3002813) Dosing Regimens in Adults With Early Alzheimer's Disease (TRAILBLAZER-ALZ 6)

Status:
Not yet recruiting
Trial end date:
2025-05-13
Target enrollment:
0
Participant gender:
All
Summary
This study will investigate different donanemab dosing regimens and their effect on the frequency and severity of ARIA-E in adults with early symptomatic Alzheimer's disease (AD) and explore participant characteristics that might predict risk of ARIA.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Eli Lilly and Company
Criteria
Inclusion Criteria:

- Gradual and progressive change in memory function reported by the participant or
informant for ≥6 months.

- A mini mental state examination (MMSE) score of 20 to 28 (inclusive) at screening.

- Have an amyloid PET scan result from central read, consistent with the presence of
amyloid pathology.

Exclusion Criteria:

- Have significant neurological disease affecting the central nervous system other than
AD, that may affect cognition or ability to complete the study, including but not
limited to, other dementias, serious infection of the brain, Parkinson's disease,
multiple concussions, or epilepsy or recurrent seizures, except febrile childhood
seizures.

- Has current serious or unstable illnesses including cardiovascular, hepatic, renal,
gastroenterologic, respiratory, endocrinologic, neurologic (other than AD),
psychiatric, immunologic, or hematologic disease and other conditions that, in the
investigator's opinion, could interfere with the analyses in this study.

- A life expectancy of <24 months

- Have a presence or history of malignant neoplasms within the past 5 years prior to
Visit 1.

Exceptions:

- non-metastatic basal- or squamous-cell skin cancer

- Stage 0 non-invasive carcinoma of the cervix

- Stage 0 non-invasive prostate cancer, or

- other cancers with low risk of recurrence or spread

- Contraindication to MRI or PET scans

- Have had prior treatment with a passive anti-amyloid immunotherapy.