Kisunla™
Understanding Kisunla™
Kisunla™ (donanemab-azbt) is an FDA-approved treatment designed for adults with early symptomatic Alzheimer’s disease (AD), including those at the mild cognitive impairment (MCI) or mild dementia stages. This therapy provides a targeted approach for managing early symptoms of AD, potentially slowing disease progression and improving cognitive function.
How Kisunla™ Works:
- Targets and clears amyloid plaques in the brain, a key driver of Alzheimer’s disease
- Designed for early intervention, offering potential benefits in preserving cognitive function
- Helps slow disease progression in individuals diagnosed with early symptomatic AD
FDA Approval:
- Kisunla™ (donanemab-azbt): Approved on July 2, 2024, for the treatment of early symptomatic Alzheimer’s disease.
For more information, please visit the Kisunla™ patient website and speak with your healthcare provider to determine if Kisunla™ is the right treatment option for you.

Referral Form: |
WHAT IT TREATS: |
MANUFACTURER: Eli Lilly and Company |
CLASS: Amyloid Beta-Directed Antibody |
PRESCRIBED BY:
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HOW ADMINISTERED: IV Infusion |
FREQUENCY: Every four weeks
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Length of infusion: About 30 mins |
FOR MORE INFORMATION: |