Lecanemab
Humanized | |
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Target | Amyloid beta |
Clinical data | |
Trade names | Leqembi |
Other names | BAN2401, lecanemab-irmb |
AHFS/Drugs.com | Monograph |
License data | |
Intravenous | |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
CAS Number | |
DrugBank | |
ChemSpider |
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UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6544H10088N1744O2032S46 |
Molar mass | 147181.62 g·mol−1 |
Lecanemab, sold under the brand name Leqembi, is a
Lecanemab was granted
Medical uses
Lecanemab is
Adverse effects
Lecanemab may cause amyloid-related imaging abnormalities (ARIA). ARIA is often asymptomatic, but serious and life-threatening events rarely may occur. ARIA most commonly presents as temporary swelling of the brain that usually resolves over time and may be accompanied by small spots of bleeding in or on the surface of the brain, though some people may have symptoms such as headache, confusion, dizziness, vision changes, nausea and seizure.[3][4] Compared to placebo, all doses of the drug caused accelerated brain shrinkage.[7]
Pharmacology
Mechanism of action
Lecanemab is a
Efficacy Study
In a
History
In July 2022, the US Food and Drug Administration (FDA) accepted an application for accelerated approval for lecanemab.[13]
In September 2022,
In November 2022, it was announced that the drug was a success in clinical trials, and exceeded its goal in reaching primary endpoints.[17]
The efficacy of lecanemab was evaluated in a double-blind, placebo-controlled, parallel-group, dose-finding study of 856 participants with Alzheimer's disease.
The FDA approved lecanemab in January 2023, via the accelerated approval pathway for the treatment of Alzheimer's disease.[3] The FDA granted the application for lecanemab fast track, priority review, and breakthrough therapy designations.[3] The approval of Leqembi was granted to Eisai R&D Management Co., Ltd.[3] In July 2023, the FDA converted lecanemab to traditional approval.[4]
Efficacy of lecanemab was evaluated using the results of Study 301 (CLARITY AD), a phase III randomized, controlled clinical trial.[4] Study 301 was a multicenter, randomized, double-blind, placebo-controlled, parallel-group study that enrolled 1,795 participants with Alzheimer's disease.[4] Treatment was initiated in participants with mild cognitive impairment or mild dementia stage of disease and confirmed presence of amyloid beta pathology.[4] Participants were randomized in a 1:1 ratio to receive placebo or lecanemab at a dose of 10 milligrams (mg)/kilograms (kg), once every two weeks.[4] Lecanemab demonstrated a statistically significant and clinically meaningful reduction of decline from baseline to 18 months on the primary endpoint, the Clinical Dementia Rating Scale Sum of Boxes score, compared to placebo.[4] Statistically significant differences between treatment groups were also demonstrated on all secondary endpoints, which included the Alzheimer's Disease Assessment Scale Cognitive Subscale 14, and the Alzheimer's Disease Cooperative Study-Activities of Daily Living Scale for Mild Cognitive Impairment.[4]
Society and culture
Legal status
In January 2023, the FDA granted accelerated approval for lecanemab.[3][18] In July 2023, the FDA converted lecanemab to traditional approval.[4]
Reception
In October 2023, lecanemab was designated as a Do Not Use drug by Public Citizen's Health Research Group.[19] It had urged the FDA not to approve it, arguing that there were serious safety concerns and very small treatment benefits. [19]
Economics
Lecanemab pricing is US$26,500 per year,[20] with a company-estimated "per-patient societal value" of US$37,600.[21] However, cost-effectiveness analysis by the Institute for Clinical and Economic Review (ICER) concluded that a broad range of $8,900 to $21,500 would be appropriate.[22] According to an estimate by the manufacturer, Eisai, about 85% of eligible early-Alzheimer's patients in the United States are covered by Medicare.[21]
After reviewing the clinical evidence and considering the treatments' other potential benefits, disadvantages, and contextual considerations noted above, the California Technology Assessment Forum unanimously concluded that lecanemab at its current pricing represents "low" long term value of money.[22] At lecanemab's current net price, approximately 5% of the 1.4 million US patients eligible for Alzheimer's disease treatment that targets beta-amyloid could be treated within five years without crossing the ICER potential budget impact threshold of $777 million per year.[22] As a result, ICER issued an access and affordability alert for lecanemab in the management of Alzheimer's disease. This alert indicates that the health care costs of the treatment might stress the health system in the short term, resulting in the displacement of other services and a rapid increase in insurance costs.[22]
Names
Lecanemab is the international nonproprietary name.[23]
Research
Lecanemab was jointly developed by the companies Eisai and Biogen and is in clinical trials for the treatment of Alzheimer's disease.[24]
It has shown statistically significant but minor effectiveness, with studies suggesting a modest decrease in
According to a phase III clinical trial (n = 1795), lecanemab has been associated with both ARIA-E (
References
- FDA. Retrieved 22 October 2023.
- ^ a b c d e "Leqembi- lecanemab injection, solution". DailyMed. 11 January 2023. Archived from the original on 15 January 2023. Retrieved 21 January 2023.
- ^ a b c d e f g h i j k "FDA Grants Accelerated Approval for Alzheimer's Disease Treatment" (Press release). U.S. Food and Drug Administration (FDA). 6 January 2023. Archived from the original on 7 January 2023. Retrieved 7 January 2023. This article incorporates text from this source, which is in the public domain.
- ^ a b c d e f g h i j k "FDA Converts Novel Alzheimer's Disease Treatment to Traditional Approval". U.S. Food and Drug Administration (FDA) (Press release). 6 July 2023. Archived from the original on 6 July 2023. Retrieved 6 July 2023. This article incorporates text from this source, which is in the public domain.
- ^ "Drug Approval Package: Leqembi". U.S. Food and Drug Administration (FDA). 6 February 2023. Archived from the original on 9 July 2023. Retrieved 8 July 2023.
- ^ "Lecanemab Summary Review" (PDF). Center for Drug Evaluation and Research (CDER). U.S. Food and Drug Administration (FDA). Archived (PDF) from the original on 7 January 2023. Retrieved 7 January 2023.
- PMID 37389302.
- PMID 25031633.
- PMID 29592816.
- ^ "Lecanemab, the New Alzheimer's Treatment: 3 Things To Know". Yale Medicine. Archived from the original on 7 December 2023. Retrieved 7 December 2023.
- ^ S2CID 254094094.
- PMID 18695059.
- ^ a b "Lecanemab Confirmatory Phase 3 Clarity Ad Study Met Primary Endpoint, Showing Highly Statistically Significant Reduction of Clinical Decline in Large Global Clinical Study of 1,795 Participants With Early Alzheimer's Disease" (Press release). Biogen. 27 September 2022. Archived from the original on 27 September 2022. Retrieved 28 September 2022.
- ^ Robbins R, Belluck P (27 September 2022). "Alzheimer's Drug Slows Cognitive Decline in Key Study". The New York Times. Archived from the original on 28 September 2022. Retrieved 28 September 2022.
- ^ "A Study to Confirm Safety and Efficacy of Lecanemab in Participants With Early Alzheimer's Disease (Clarity AD)". ClinicalTrials.gov. 11 July 2022. Archived from the original on 28 September 2022. Retrieved 28 September 2022.
- ^ Sample I (22 November 2022). "'This looks like the real deal': Are we inching closer to a treatment for Alzheimer's?". The Guardian. Archived from the original on 10 January 2023.
- ^ Gallagher J (30 November 2022). "Alzheimer's drug lecanemab hailed as momentous breakthrough". BBC News Online. Archived from the original on 2 December 2022. Retrieved 30 November 2022.
- ^ Howard J, Goodman B (6 January 2023). "Alzheimer's drug lecanemab receives accelerated approval amid safety concerns". CNN. Archived from the original on 6 January 2023. Retrieved 11 January 2023.
- ^ a b ""Lecanemab for Alzheimer's Disease: Do Not Use"". Worst Pills, Best Pills News. Vol. 29, no. 10. Public Citizen. 1 October 2023.
- ^ "Eisai's Approach To U.S. Pricing For Leqembi (Lecanemab), a Treatment For Early Alzheimer's Disease, Sets Forth Our Concept Of "Societal Value Of Medicine" In Relation To "Price Of Medicine"" (Press release). Eisai Inc. 6 January 2023. Archived from the original on 7 January 2023. Retrieved 7 January 2023 – via PR Newswire.
- ^ a b Bell J (6 February 2023). "Eisai gives first glimpse into Alzheimer's drug launch". BiopharmaDive. Archived from the original on 12 February 2023. Retrieved 11 February 2023.
- ^ a b c d "ICER Publishes Final Evidence Report on Lecanemab for Alzheimer's Disease" (Press release). Institute for Clinical and Economic Review. 17 April 2023. Archived from the original on 7 May 2023. Retrieved 7 May 2023.
- hdl:10665/340680.
- ^ Clinical trial number NCT01767311 for "Study to Evaluate Safety, Tolerability, and Efficacy of BAN2401 in Subjects With Early Alzheimer's Disease" at ClinicalTrials.gov
- ^ Devlin H (28 September 2022). "Success of experimental Alzheimer's drug hailed as 'historic moment'". The Guardian. Archived from the original on 28 September 2022.
Further reading
- Tolar M, Abushakra S, Hey JA, Porsteinsson A, Sabbagh M (August 2020). "Aducanumab, gantenerumab, BAN2401, and ALZ-801-the first wave of amyloid-targeting drugs for Alzheimer's disease with potential for near term approval". Alzheimer's Research & Therapy. 12 (1): 95. PMID 32787971.
- Villain N, Planche V, Levy R (December 2022). "High-clearance anti-amyloid immunotherapies in Alzheimer's disease. Part 1: Meta-analysis and review of efficacy and safety data, and medico-economical aspects". Revue Neurologique. 178 (10): 1011–1030. PMID 36184326.