Leqembi (lecanemab or lecanemab-irmb) is an injectable monoclonal antibody that's used to treat people with mild Alzheimer's disease. It was approved by the FDA in January 2023 through the accelerated approval pathway. But as of July 2023, the medication has full FDA approval to treat Alzheimer's disease. Leqembi (lecanemab) is infused into a vein by a trained healthcare provider once every 2 weeks. Common side effects include infusion-related reactions and headache. Note that Leqembi (lecanemab) isn't a cure for Alzheimer's disease.
Alzheimer’s disease (mild cognitive impairment)
Leqembi (lecanemab) is an amyloid beta-directed monoclonal antibody. This means that it targets a protein in the brain called amyloid beta (also called beta-amyloid). These proteins clump together in Alzheimer's disease to form plaques that can be toxic for your brain cells.
Leqembi (lecanemab) works to lessen the buildup of these plaques in the brain. Some researchers believe that lessening amyloid beta plaques in the brain can slow Alzheimer's from getting worse. But more studies are needed to confirm this effect.
Source: DailyMed
Side effects that you should report to your care team as soon as possible:
Side effects that usually do not require medical attention (report these to your care team if they continue or are bothersome):
Given once every 2 weeks
Lessens amyloid beta plaques in the brain
Can slow down worsening of Alzheimer's disease in people with mild symptoms
No known interactions with other medications
Brand-name medication only
Only available as an IV infusion that's given by a healthcare provider
Must get MRI scans before and during treatment
Not studied in people with moderate or severe Alzheimer's disease
Make sure to put your Leqembi (lecanemab) infusions and MRI appointments on a calendar so you don't miss any doses. Have a caregiver help you keep track of your appointments.
If you miss an appointment for your Leqembi (lecanemab) infusion, call your provider to schedule your next dose as soon as possible.
Bring a book or something to do to help pass the time during your Leqembi (lecanemab) infusion. Each infusion takes about 1 hour, but it can sometimes take longer depending on whether you have reactions to the infusion.
Tell your provider if you're taking medications that help lower the risk for blood clots (e.g., aspirin, blood thinners). Your provider will want to monitor you more closely for possible bleeding problems in your brain while you're taking Leqembi (lecanemab).
You're encouraged to enroll in the Alzheimer’s Network for Treatment and Diagnostics (ALZ-NET). This voluntary registry monitors your safety while you're taking Leqembi (lecanemab). Its purpose is to help researchers learn more about the risks of treatment for Alzheimer's disease. Ask your provider for more information.
Leqembi (lecanemab) can cause some serious health issues. This risk may be even higher for certain groups. If this worries you, talk to your doctor or pharmacist about other options.
Risk factors: Being a carrier of the apolipoprotein E ε4 (ApoE ε4) gene
ARIA most commonly happens early in treatment (within the first 7 doses), but can happen at anytime, and you can have more than one episode. ARIA can also happen to anyone, but the risk appears to be higher for those with the ApoE ε4 gene. There's a test available to see if you have this gene.
Make sure to check with your provider before you start taking any new medications. Certain medications like aspirin or clopidogrel (Plavix) might raise your risk of bleeding in the brain.
Most people with ARIA don't notice any symptoms, so you'll need to get MRI scans done before and during treatment to watch out for it. If you do have symptoms, they tend to go away over time. But some can be more serious and rarely life threatening. Contact your provider right away if you have a headache, vision changes, dizziness, nausea, trouble walking, or a seizure.
Leqembi (lecanemab) can cause infusion-related reactions, which can include chills, muscle or joint pain, nausea, vomiting, and changes in blood pressure. These reactions are mostly mild, but some can be serious. In studies, most reactions happened with the first infusion.
Tell your provider if you feel unwell, have trouble breathing, or feel like your chest is pounding during your Leqembi (lecanemab) infusion. Your provider might slow down the infusion. But in some cases, your provider might need to stop the infusion altogether. If you have an infusion-related reaction, your provider might give you medications for you to take before your next dose to lower your chance of having another reaction.
In some rare cases, Leqembi (lecanemab) can cause serious allergic reactions, including severe swelling and anaphylaxis. Get medical help right away if you notice hives, swelling in your face or throat, or trouble breathing.
Leqembi (lecanemab) is given as an intravenous (IV) infusion by a healthcare provider.
The typical dose is 10 mg/kg of body weight given once every 2 weeks.
By signing up, I agree to GoodRx's Terms and Privacy Policy, and to receive marketing messages from GoodRx.
Abushakra, S., et al. (2023). Prevalence of amyloid-related imaging abnormalities in APOE4/4 homozygotes with early Alzheimer’s disease: Baseline findings from ongoing clinical trials of oral anti-amyloid agent ALZ-801 (valiltramiprosate) (P5-6.003). Neurology.
Biogen Inc. (2022). Eisai presents full results of lecanemab phase 3 confirmatory clarity ad study for early Alzheimer’s disease at clinical trials on Alzheimer’s disease (Ctad) conference. PRNewswire.
Eisai Co., Ltd. (2023). FDA grants traditional approval for Leqembi® (lecanemab-irmb) for the treatment of Alzheimer’s disease.
Eisai Inc. (2024). Leqembi- lecanemab injection, solution [package insert]. DailyMed.
Knopman, D. S., et al. (2020). Failure to demonstrate efficacy of aducanumab: An analysis of the EMERGE and ENGAGE trials as reported by Biogen, December 2019. Alzheimer's & Dementia.
National Institute on Aging. (2024). What happens to the brain in Alzheimer's disease?
Söderberg, L., et al. (2022). Lecanemab, aducanumab, and gantenerumab — Binding profiles to different forms of amyloid-beta might explain efficacy and side effects in clinical trials for Alzheimer’s disease. Neurotherapeutics.
Sperling, R. A., et al. (2011). Amyloid-related imaging abnormalities in amyloid-modifying therapeutic trials: Recommendations from the Alzheimer's Association Research Roundtable Workgroup. Alzheimer's & Dementia.
U.S. Food and Drug Administration. (2021). Aducanumab (marketed as Aduhelm) information.
U.S. Food and Drug Administration. (2023). FDA converts novel Alzheimer’s disease treatment to traditional approval.
U.S. Food and Drug Administration. (2023). FDA converts novel Alzheimer’s disease treatment to traditional approval.
U.S. Food and Drug Administration. (2023). FDA grants accelerated approval for Alzheimer’s disease treatment.
van Dyck, C. H., et al. (2022). Lecanemab in early Alzheimer’s disease. The New England Journal of Medicine.
Research prescriptions and over-the-counter medications from A to Z, compare drug prices, and start saving.