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Kisunla

Pronunciation: kih-SUHN-lah
Generic name: donanemab
Dosage form: injection for intravenous use (350 mg/20 mL)
Drug class: Miscellaneous central nervous system agents

Medically reviewed by Melisa Puckey, BPharm. Last updated on July 13, 2025.

What is Kisunla?

Kisunla is a prescription medicine used for Alzheimer’s disease (AD) in patients with mild cognitive impairment (MCI) or mild dementia. Kisunla helps slow down the decline in memory, thinking, and daily functioning, which slows Alzheimer’s disease progression, and people can continue living their lives doing their daily activities and hobbies for a longer time.

Alzheimer's disease symptoms are thought to be related to clumps of amyloid protein (amyloid plaques) that can occur in the brain. Kisunla is an anti-amyloid treatment that works by reducing amyloid beta plaques in the brain, which slows the progression of Alzheimer’s disease. Kisunla is called an amyloid beta-directed antibody. 

Kisunla (donanemab) is administered as a once-monthly IV infusion that takes approximately 30 minutes. The dose is increased slowly over the first 4 infusions to reduce the risk of side effects.

Kisunla FDA approval was granted on July 2, 2024, to Eli Lilly and Company after positive results from the TRAILBLAZER-ALZ 2 clinical trial.

How well does it work?

Kisunla (donanemab) significantly slowed Alzheimer's disease progression by more than 20% at 76 weeks in the TRAILBLAZER-ALZ 2  clinical trial. This was measured using the Integrated Alzheimer’s Disease Rating Scale (iADRS) and Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) score in patients with low/medium tau and in the combined low/medium and high tau populations.

Treatment with Kisunla benefited all groups of trial participants, but patients in earlier stages of the disease showed the most significant improvements.

Kisunla side effects 

Common Kisunla side effects

Common Kisunla side effects include headache and swelling in areas of the brain with or without small spots of bleeding in or on the brain's surface. These occurred in at least 10% of patients and at a higher incidence compared to placebo. 

Serious Kisunla side effects 

This is not a complete list of side effects, and others may occur. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

 Also, see the Warning section

Warnings

Kisunla can cause serious side effects, including:

Amyloid Related Imaging Abnormalities or ARIA.

ARIA is a common side effect that does not usually cause any symptoms, but sometimes serious symptoms can occur. ARIA can be fatal. It is most commonly seen in an MRI as temporary swelling in areas of the brain that usually resolves over time. Some people may also have small spots of bleeding in or on the surface of the brain, and infrequently, larger areas of bleeding in the brain can occur. 

Most people who develop ARIA do not have symptoms; however, some people may have symptoms such as headache, dizziness, nausea, difficulty walking, confusion, vision changes, and seizures.

If you have any of the symptoms of ARIA listed above, you should call your healthcare provider or go to the nearest hospital emergency room right away. 

You are more at risk of ARIA if you have a genetic risk factor (homozygous apolipoprotein E ε4 gene carriers). Your healthcare provider may test to see if you have this risk factor.

If you take medicines to reduce blood clots from forming (antithrombotic medicines) while receiving Kisunla, you may be at a higher risk of developing bleeding in the brain.

Magnetic resonance imaging (MRI) scans are done before and during your treatment to check you for ARIA.

You should carry information that you are receiving Kisunla, which can cause ARIA, and that ARIA symptoms can look like stroke symptoms.

There are registries that collect information on treatments for Alzheimer’s disease. Your healthcare provider can help you become enrolled in these registries. 

Consider the risk of ARIA and the benefit of Alzheimer's disease when deciding to treat with Kisunla.

Who should not take Kisunla?

You should not receive this medicine if you have had serious allergic reactions to donanemab-azbt or any of the ingredients in this infusion. See the end of this document for a complete list of ingredients.

Before taking this medicine

Pregnancy

Tell your healthcare provider if you plan to become pregnant, become pregnant, or are pregnant, as it is not known if this medicine will harm your unborn baby.

Breastfeeding

Tell your healthcare provider if you are breastfeeding or plan to breastfeed, as it is not known if the active ingredient in Kisunla passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby while receiving this medicine.

How will I receive this medicine?

Kisunla is administered as an infusion into a vein (IV infusion) in your arm, which will last about 30 minutes.
Kisunla is given every 4 weeks with an initial increasing dosing schedule. If you miss an infusion, you should receive your next dose as soon as possible.

Kisunla dosing information

Kisunla is given every 4 weeks with an initial increasing dosing schedule.

Usual Adult Kisunla dose is every 4 weeks:

Comments

Dose modifications may be required for patients with ARIA-E and ARIA-H 

Kisunla is available as: 350 mg/20 mL (17.5 mg/mL) in a single-dose vial.

Interactions

Other drugs may interact with Kisunla, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible drug interactions are listed here.

Does Kisunla interact with my other drugs?

Enter medications to view a detailed interaction report using our Drug Interaction Checker.

Kisunla Package Insert 

HCPs and patients often use the Kisunla Package Insert (PI) brand for more detailed information about this medicine. The Package Insert contains more comprehensive information on Indications and Usage, Dosage and Administration, Clinical Pharmacology, Clinical Studies, Drug Interaction, and more. Discuss any medical questions you have with your HCP (health care professional). This is not all the information you need to know about this medicine for safe and effective use, and it does not take the place of talking to your doctor about your treatment.

The Package Insert is sometimes called  Kisunla Prescribing Information (PI) or FDA label.

Storage

Unopened Vial 

Store refrigerated at 2°C to 8°C (36°F to 46°F). 

Keep the vial in the outer carton to protect it from light.

Do not freeze or shake.

If refrigeration is not available, it may be stored at room temperature (20°C to 25°C [68°F to 77°F]) for up to 3 days.

Diluted Solution

After dilution, immediate use is recommended.

Diluted solution may be stored refrigerated at 2°C to 8°C (36°F to 46°F) for up to 72 hours or at room temperature (20°C to 25°C [68°F to 77°F]) for up to 12 hours.

Do not freeze the diluted solution. 

Storage times include the duration of infusion.

Ingredients

Active ingredient: donanemab-azbt

Inactive ingredients: anhydrous citric acid, polysorbate 80, sodium citrate, sucrose, and Water for Injection, USP.

Manufacturer

Eli Lilly and Company, Indianapolis, IN 46285, USA

Kisunla Biosimilars

Biosimilar and interchangeable products are biological products that are highly similar to and have no clinically meaningful differences from the reference product.

Reference products

These are biological products that have already been approved by the FDA, against which biosimilar products are compared. There is 1 for Kisunla.

Kisunla (donanemab-azbt) - Eli Lilly and Company
Formulation type Strength
Single-Dose Vial 350 mg/20 mL (17.5 mg/mL)

Popular FAQ

How do I decide between Leqembi and Kisunla?

Leqembi (lecanemab-irmb) and Kisunla (donanemab-azbt) are two injectable treatments for Alzheimer’s disease. While both medications work by reducing amyloid plaques in the brain, there are some differences to consider when deciding between the two. These include effectiveness, side effects, and cost. Continue reading

Will insurance cover Kisunla treatment?

Kisunla treatment typically requires a prior authorization approval from your commercial insurance company before they will pay for it. Medicare Part B may pay for Kisunla and brain imaging scans if you are eligible, but you must first meet your yearly deductible and then pay coinsurance costs, which are usually 20%. Continue reading

How well does Kisunla work?

In studies, treatment with Kisunla significantly slowed Alzheimer's disease clinical decline when compared to a group who received a placebo. People with the least advanced disease experienced the strongest outcomes, with a 35% slowing of decline on the iADRS score, which measures memory, thinking, and daily functioning. Continue reading

How long will I need to take Kisunla?

The length of treatment with Kisunla (donanemab-azbt) for Alzheimer's disease is different for each person. The recommended dose is 700 mg given by intravenous infusion every 4 weeks for three doses, and then 1,400 mg every 4 weeks. Continue reading

How quickly does Kisunla start working?

In the TRAILBLAZER-ALZ 2 study with 1,736 people, those with the least advanced disease experienced the strongest outcomes, with a 35% slowing of cognitive and functional decline at 76 weeks on the Integrated Alzheimer’s Disease Rating Scale (iADRS), a tool which measures memory, thinking, and daily functioning. Continue reading

Can Kisunla be used with other Alzheimer's drugs?

Yes, Kisunla (donanemab-azbt) can be used with other Alzheimer’s drugs. Clinical trials of Kisunla that led to its FDA approval included both people with Alzheimer’s disease who were taking other treatments and people who were not. Continue reading

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.