BioArctic: New data on lecanemab presented at the 2024 AD/PD™ congress

Rhea-AI Summary

BioArctic AB and Eisai present new data on lecanemab at the 2024 International Conference on Alzheimer's and Parkinson's Diseases. The data highlights the efficacy and safety of lecanemab in treating Alzheimer's disease, showing promising results in reducing Aβ protofibrils and plaques in the brain. The collaboration between BioArctic and Eisai has been instrumental in the development and regulatory submissions of lecanemab.

Medical Research Analyst

The presentation of new data on lecanemab at the International Conference on Alzheimer's and Parkinson's Diseases offers insights into the drug's potential efficacy and safety in treating Alzheimer's disease. Lecanemab's unique binding properties to both soluble and insoluble amyloid-beta aggregates could position it favorably in the competitive landscape of Alzheimer's treatments. The lower incidence of Amyloid-related imaging abnormalities (ARIA), which are side effects associated with anti-amyloid-beta antibodies, could be a significant differentiator for lecanemab, potentially leading to a stronger safety profile compared to its competitors.

Extended efficacy results from the Phase 3 Clarity AD open label extension study up to 30 months suggest a sustained benefit from lecanemab treatment. This is particularly relevant as Alzheimer's disease requires long-term management and treatments that can demonstrate prolonged efficacy are likely to be more attractive to clinicians and patients. Moreover, data indicating that early intervention could be more impactful underscores the importance of early diagnosis and could influence future screening and treatment protocols.

Market Research Analyst

The strategic collaboration between BioArctic and Eisai, with the latter leading development and regulatory submissions, is a key factor in lecanemab's commercial trajectory. Eisai's global reach and Biogen's co-promotion efforts could expedite market penetration upon approval. BioArctic's commercial rights in the Nordic region, contingent on European approval, may provide a foothold in a market that is often characterized by high standards of healthcare and an openness to innovative treatments.

Investor interest in BioArctic and Eisai is likely to be influenced by the outcomes of these studies, as positive data can lead to increased confidence in the drug's commercial success. The focus on early-stage Alzheimer's treatment also taps into a growing market segment, as the medical community emphasizes early detection and intervention. This could expand the target demographic and potentially increase the total addressable market for lecanemab.

Economist

The economic implications of an effective Alzheimer's treatment like lecanemab are vast. Alzheimer's disease has a significant impact on healthcare systems worldwide due to the costs associated with long-term care and the loss of productivity from both patients and caregivers. A treatment that can slow the progression of the disease or improve cognitive function can lead to substantial cost savings for healthcare providers and society at large. The potential for early intervention to stabilize the disease process could further enhance these economic benefits by delaying the onset of severe symptoms and reducing the need for intensive care services.

Additionally, the market for Alzheimer's treatments is substantial, with a growing patient population due to aging demographics. A successful entry of lecanemab into this market could result in considerable revenue streams for BioArctic and Eisai, with the potential to recoup research and development costs and fund future innovation. This can have a positive effect on their stock valuations and investor sentiment, particularly if lecanemab becomes a first-line treatment option due to its safety and efficacy profile.

STOCKHOLM, March 11, 2024 /PRNewswire/ -- BioArctic AB (publ) (Nasdaq Stockholm: BIOA B) and its partner Eisai presented new data on lecanemab (brand name: Leqembi®) at the 2024 International Conference on Alzheimer's and Parkinson's Diseases and related neurological disorders (AD/PD™), held in Lisbon, Portugal and virtually, March 5–9.

BioArctic's founder, Professor Lars Lannfelt, presented data on the binding properties of the anti-amyloid-beta (Aβ) antibody lecanemab and other anti Aβ antibodies. Lecanemab was designed to preferentially bind soluble (protofibrils), as well as insoluble Aβ aggregates (fibrils), to reduce both Aβ protofibrils and Aβ plaques in the brain. The difference in binding to CAA^[1] was presented, with lecanemab having lower binding to CAA than most other antibodies. This could explain the difference in the adverse event ARIA^[2] seen between different antibodies, with lecanemab showing relatively low incidence of ARIA.

In another presentation Professor Christopher van Dyke presented extended efficacy results from the Phase 3 Clarity AD open label extension study of lecanemab in Alzheimer's disease up to 30 months, showing continued benefit with lecanemab treatment. Professor van Dyke also highlighted data from the tau sub-study of Clarity AD, which showed that all cohorts of the tau population benefitted from treatment with lecanemab. Data from the low tau population, representing earlier stages of the disease, indicated that intervening in early stages of disease may be particularly impactful in stabilizing the disease process.

"It is inspiring to see all the data presented at the conference further strengthening lecanemab's efficacy and safety results, specifically from the earlier cohorts of patients which alludes to the importance of early diagnosis and treatment," said Gunilla Osswald, CEO at BioArctic. "It has also been impressive to see how the field is moving forward, and we have seen encouraging data regarding both alpha-synuclein and blood brain barrier transportation approaches."

Lecanemab is the result of a long-standing collaboration between BioArctic and Eisai, and the anti Aβ protofibril antibody was originally developed by BioArctic based on the work of Professor Lars Lannfelt and his discovery of the Arctic mutation in Alzheimer's disease.

Eisai serves as the lead of lecanemab development and regulatory submissions globally with both Eisai and Biogen co-commercializing and co-promoting the product and Eisai having final decision-making authority. BioArctic has the right to commercialize lecanemab in the Nordic region, pending European approval, and currently Eisai and BioArctic are preparing for commercialization in the region.

This release discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy or safety. There is no guarantee that such investigational agents will successfully complete clinical development or gain health authority approval.

The information was released for public disclosure, through the agency of the contact persons below, on March 11, 2024, at 08.00 a.m. CET.

For further information, please contact: 

Oskar Bosson, VP Communications and IR
E-mail: oskar.bosson@bioarctic.se
Phone: +46 70 410 71 80 

Jiang Millington, Director Corporate Communication and Social Media
E-mail: jiang.millington@bioarctic.se
Phone: +46 79 33 99 166

About lecanemab (generic name, U.S., Japan and China brand name: Leqembi®)

Lecanemab is the result of a strategic research alliance between BioArctic and Eisai. Lecanemab is a humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody directed against aggregated soluble (protofibril) and insoluble forms of amyloid-beta (Aβ). In the U.S., Leqembi was granted traditional approval by the US Food and Drug Administration (FDA) on July 6, 2023. Leqembi is indicated as a disease-modifying treatment for Alzheimer's disease (AD) in the US. Treatment with Leqembi should be initiated in patients with mild cognitive impairment (MCI) or mild dementia stage of disease, the population in which treatment was initiated in clinical trials. Please see full U.S. Prescribing Information.

In Japan, Eisai received approval from the Ministry of Health, Labour and Welfare (MHLW) on September 25, 2023, to manufacture and market lecanemab as a treatment for slowing progression of MCI and mild dementia due to AD. Furthermore, in China, Leqembi was approved by the National Medical Products Administration (NMPA) as a treatment of MCI due to AD and mild AD dementia in January 2024.

Eisai has also submitted applications for approval of lecanemab in 14 different countries, including EU, Canada and Great Britain.

Eisai has completed a lecanemab subcutaneous bioavailability study, and subcutaneous dosing is currently being evaluated in the Clarity AD (Study 301) open-label extension (OLE) study. A maintenance dosing regimen has been evaluated as part of the Phase 2b study (Study 201).

Since July 2020 Eisai's Phase 3 clinical study (AHEAD 3-45) for individuals with preclinical AD, meaning they are clinically normal and have intermediate or elevated levels of amyloid in their brains, is ongoing. AHEAD 3-45 is conducted as a public-private partnership between the Alzheimer's Clinical Trial Consortium that provides the infrastructure for academic clinical trials in AD and related dementias in the U.S, funded by the National Institute on Aging, part of the National Institutes of Health and Eisai.

Since January 2022, the Tau NexGen clinical study for Dominantly Inherited AD (DIAD), that is conducted by Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU), led by Washington University School of Medicine in St. Louis, is ongoing and includes lecanemab as the backbone anti-amyloid therapy.

About the collaboration between BioArctic and Eisai

Since 2005, BioArctic has a long-term collaboration with Eisai regarding the development and commercialization of drugs for the treatment of Alzheimer's disease. The most important agreements are the Development and Commercialization Agreement for the lecanemab antibody, which was signed 2007, and the Development and Commercialization agreement for the antibody Leqembi back-up for Alzheimer's disease, which was signed 2015. In 2014, Eisai and Biogen entered into a joint development and commercialization agreement for lecanemab. Eisai is responsible for the clinical development, application for market approval and commercialization of the products for Alzheimer's disease. BioArctic has the right to commercialize lecanemab in the Nordic region under certain conditions and is currently preparing for commercialization in the Nordics together with Eisai. BioArctic has no development costs for lecanemab in Alzheimer's disease and is entitled to payments in connection with regulatory approvals, and sales milestones as well as royalties on global sales.

About BioArctic AB

BioArctic AB (publ) is a Swedish research-based biopharma company focusing on innovative treatments that can delay or stop the progression of neurodegenerative diseases. The company invented Leqembi® (lecanemab) - the world's first drug proven to slow the progression of the disease and reduce cognitive impairment in early Alzheimer's disease. Leqembi has been developed together with BioArctic's partner Eisai, who are responsible for regulatory interactions and commercialization globally. In addition to Leqembi, BioArctic has a broad research portfolio with antibodies against Parkinson's disease and ALS as well as additional projects against Alzheimer's disease. Several of the projects utilize the company's proprietary BrainTransporter™ technology, which has the potential to actively transport antibodies across the blood-brain barrier to enhance the efficacy of the treatment. BioArctic's B share (BIOA B) is listed on Nasdaq Stockholm Large Cap. For further information, please visit www.bioarctic.se.

^[1] CAA, or cerebral amyloid angiopathy, is a condition characterized by the accumulation of amyloid proteins in the walls of the blood vessels in the brain.

^[2] ARIA, or Amyloid-Related Imaging Abnormalities, refers to changes seen on MRI scans associated with amyloid-targeting therapies for Alzheimer's disease, and can manifest as edema (ARIA-E) or hemorrhage (ARIA-H)

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/bioarctic/r/new-data-on-lecanemab-presented-at-the-2024-ad-pd--congress,c3943470

The following files are available for download:

https://mb.cision.com/Main/9978/3943470/2659208.pdf

New data on lecanemab presented at the 2024 AD/PDâ„¢ congress

 

View original content:https://www.prnewswire.com/news-releases/bioarctic-new-data-on-lecanemab-presented-at-the-2024-adpd-congress-302085063.html

SOURCE BioArctic

What data was presented at the 2024 International Conference on Alzheimer's and Parkinson's Diseases regarding lecanemab?

The data presented highlighted the binding properties of lecanemab, its efficacy in reducing Aβ protofibrils and plaques in the brain, and its lower incidence of ARIA compared to other antibodies.

Who presented the extended efficacy results of lecanemab in Alzheimer's disease?

Professor Christopher van Dyke presented the extended efficacy results of lecanemab in Alzheimer's disease.

What was highlighted in the tau sub-study of the Phase 3 Clarity AD study?

The tau sub-study of the Phase 3 Clarity AD study showed that all cohorts of the tau population benefitted from treatment with lecanemab, particularly in stabilizing the disease process in early stages.

What is the collaboration between BioArctic and Eisai regarding lecanemab?

BioArctic and Eisai have a long-standing collaboration in the development and regulatory submissions of lecanemab, with Eisai leading the development and regulatory submissions globally.

Who has the right to commercialize lecanemab in the Nordic region?

BioArctic has the right to commercialize lecanemab in the Nordic region, pending European approval.