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Eisai U.S. Neurology

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uuid004by9g

Namestring
Eisai U.S. Neurology
Legal namestring
Eisai Inc.
Websiteurl
eisaineuro.com
Company typeenum
Private
Founded yearstring
-
Descriptiontext

Eisai U.S. Neurology operates the American neurology franchise of Eisai Co., Ltd., a Japanese pharmaceutical company headquartered in Tokyo and listed on the Tokyo Stock Exchange (4523). The U.S. entity (legal name Eisai Inc.) is headquartered in Nutley, New Jersey, and employs 84 staff focused on neurodegenerative disease treatments, primarily Alzheimer's Disease and sleep-wake disorders. Its flagship product is LEQEMBI (lecanemab-irmb), an FDA-approved humanized IgG1 monoclonal antibody that selectively binds to amyloid-beta (Aβ) protofibrils for the treatment of early Alzheimer's Disease; the company received FDA approval on July 13, 2026 for LEQEMBI IQLIK, a subcutaneous autoinjector formulation designed as an initiation dose to replace IV administration.

The underlying technology platform centers on four decades of accumulated Alzheimer's Disease research spanning amyloid, tau, neurodegeneration, and emerging pathway targets. The company operates the G2D2 (Groundbreaking Dementia Discovery) R&D laboratory in Cambridge, MA, which pursues next-generation immunodementia drugs using a stated "deep human biology learning" approach. The portfolio is anchored by LEQEMBI's IV formulation and the newly approved subcutaneous autoinjector, supported by clinical evidence including a real-world LEADER study showing over 75% of early Alzheimer's patients remained stable over an average 17 months of treatment.

The business operates a B2B2C pharmaceutical model: Eisai distributes LEQEMBI through HCP-directed physician networks (neurology specialists and healthcare systems), pharmacy trade relations, and the Magnolia Patient Support Programs for insurance navigation and co-pay assistance. Pricing for prescription medications is not publicly disclosed and is determined through insurance coverage and patient assistance programs. The U.S. entity is restricted to U.S. residents and works alongside parent-coordinated regional entities in Canada and the EU under Eisai Co., Ltd.'s global strategic direction.

Short descriptiontext

Eisai U.S. Neurology is the U.S. subsidiary of Japan's Eisai Co., Ltd., developing and commercializing neurology therapeutics primarily for early Alzheimer's Disease through its FDA-approved LEQEMBI franchise, serving patients via healthcare providers, pharmacies, and Magnolia patient support programs.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersNutley, United States
HQ citystring
Nutley
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
neurology pharmaceuticals, alzheimer's disease therapeutics, monoclonal antibody treatments, neurodegenerative disease drugs, sleep disorder medications
Industry3 codes
1Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Cognitive & Behavioral Neurology (Dementia/Memory Disorders)
CodeHLAKAIAHPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Neurology Pharmaceuticals
Social media profiles2 records
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Marketing or Sales, Personnel, Operations, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1LEQEMBI (lecanemab-irmb)
Description

FDA-approved treatment for early Alzheimer's disease, available as IV formulation and subcutaneous injection (IQLIK).

us.eisai.com
Core offering1 text field

Eisai U.S. Neurology develops, manufactures, and markets FDA-approved pharmaceutical therapeutics for neurodegenerative conditions, with a primary focus on Alzheimer's disease. Its flagship product LEQEMBI (lecanemab-irmb) is an amyloid-targeting monoclonal antibody available in IV formulation and a newly approved subcutaneous injection (LEQEMBI IQLIK) for initiation dosing in early Alzheimer's disease. The company also pursues research across tau, neurodegeneration, immunodementia, and sleep-wake disorders (insomnia and narcolepsy).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Over 75% of early Alzheimer's patients remained stable and nearly 7% improved over average 17 months of LEQEMBI treatment
Product overview1 text field

Eisai U.S. Neurology operates as a pharmaceutical company focused on neurodegenerative disease treatments, with LEQEMBI® (lecanemab-irmb) as its flagship FDA-approved product for early Alzheimer's disease. The portfolio includes the original IV formulation and the newly approved LEQEMBI IQLIK® subcutaneous injection for treatment initiation. The company also operates G2D2, a dedicated R&D facility in Cambridge, MA pursuing next-generation immunodementia therapeutics. Research areas include amyloid targeting, tau, neurodegeneration, sleep-wake disorders (insomnia and narcolepsy), and the broader dementia pipeline.

Product and service2 records
1LEQEMBI (lecanemab-irmb)
CategoryNeurology Pharmaceuticals
Description

Humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody that selectively binds to amyloid-beta (Aβ) protofibrils. FDA-approved for the treatment of early Alzheimer's Disease and administered intravenously. Indicated for healthcare providers and patients with early-stage Alzheimer's Disease.

2LEQEMBI IQLIK (lecanemab-irmb) Subcutaneous Injection
CategoryNeurology Pharmaceuticals
Description

Subcutaneous injection formulation of lecanemab approved as an initiation dose for early Alzheimer's Disease, offering an alternative to IV administration through an autoinjector delivery system. Improves patient accessibility compared to intravenous infusion.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Biogen is the co-developer of LEQEMBI and markets competing/successor AD therapies (Aduhelm legacy, pipeline assets) — directly overlapping in disease-modifying Alzheimer's neurology with shared commercial infrastructure.

TypeBroad incumbent
Description

BMS operates a broad neuroscience and specialty therapeutics franchise with growing CNS investment — a larger incumbent competing for neurology talent, payer attention, and acquisition targets in the AD space.

TypeDirect peer
Description

Eli Lilly markets Kisunla (donanemab), a competing anti-amyloid antibody approved for early Alzheimer's Disease — directly competing with LEQEMBI in the same indication, prescriber base, and payer landscape.

TypeRegional player
Description

Otsuka is a Japanese-headquartered pharmaceutical peer with overlapping neurology/CNS focus (e.g., Abilify, CNS pipeline) — comparable therapeutic categories but operating primarily through different geographic channels and partner arrangements.

TypeBroad incumbent
Description

Roche developed gantenerumab for Alzheimer's and operates a broad neuroscience portfolio — overlapping with Eisai in CNS drug development but across a wider therapeutic footprint including oncology and rare disease.

TypeEmerging player
Description

Cognition Therapeutics is developing CT1812 for early Alzheimer's Disease, targeting the sigma-2 receptor — emerging neurology player with overlapping disease-modifying AD ambition but differentiated mechanism.

TypeEmerging player
Description

Prothena is a clinical-stage biotech developing anti-amyloid and tau-targeted therapies for neurodegenerative diseases — directly comparable pipeline focus on AD/immunodementia mechanisms with Eisai's G2D2 and LEQEMBI franchise.

TypeBroad incumbent
Description

AbbVie maintains a broad neuroscience and specialty CNS portfolio and has invested in neurodegeneration research — a larger incumbent competing for HCP mindshare and pipeline assets in CNS therapeutics.

TypeEmerging player
Description

Sage Therapeutics develops CNS therapies including Zurzuvae (postpartum depression) and pipeline neurology assets — comparable CNS-focused biopharma targeting specialty neurology prescribers with overlapping patient access infrastructure.

TypeEmerging player
Description

Acumen Pharmaceuticals is developing sabirnetug, an anti-amyloid antibody for early Alzheimer's Disease — emerging competitor pursuing the same patient population and mechanism class as LEQEMBI.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses1 record

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Eisai U.S. Neurology

Neurology Pharmaceuticalseisaineuro.com

Eisai U.S. Neurology is the U.S. subsidiary of Japan's Eisai Co., Ltd., developing and commercializing neurology therapeutics primarily for early Alzheimer's Disease through its FDA-approved LEQEMBI franchise, serving patients via healthcare providers, pharmacies, and Magnolia patient support programs.

What Eisai U.S. Neurology does

Eisai U.S. Neurology operates the American neurology franchise of Eisai Co., Ltd., a Japanese pharmaceutical company headquartered in Tokyo and listed on the Tokyo Stock Exchange (4523). The U.S. entity (legal name Eisai Inc.) is headquartered in Nutley, New Jersey, and employs 84 staff focused on neurodegenerative disease treatments, primarily Alzheimer's Disease and sleep-wake disorders. Its flagship product is LEQEMBI (lecanemab-irmb), an FDA-approved humanized IgG1 monoclonal antibody that selectively binds to amyloid-beta (Aβ) protofibrils for the treatment of early Alzheimer's Disease; the company received FDA approval on July 13, 2026 for LEQEMBI IQLIK, a subcutaneous autoinjector formulation designed as an initiation dose to replace IV administration.

The underlying technology platform centers on four decades of accumulated Alzheimer's Disease research spanning amyloid, tau, neurodegeneration, and emerging pathway targets. The company operates the G2D2 (Groundbreaking Dementia Discovery) R&D laboratory in Cambridge, MA, which pursues next-generation immunodementia drugs using a stated "deep human biology learning" approach. The portfolio is anchored by LEQEMBI's IV formulation and the newly approved subcutaneous autoinjector, supported by clinical evidence including a real-world LEADER study showing over 75% of early Alzheimer's patients remained stable over an average 17 months of treatment.

The business operates a B2B2C pharmaceutical model: Eisai distributes LEQEMBI through HCP-directed physician networks (neurology specialists and healthcare systems), pharmacy trade relations, and the Magnolia Patient Support Programs for insurance navigation and co-pay assistance. Pricing for prescription medications is not publicly disclosed and is determined through insurance coverage and patient assistance programs. The U.S. entity is restricted to U.S. residents and works alongside parent-coordinated regional entities in Canada and the EU under Eisai Co., Ltd.'s global strategic direction.

Eisai U.S. Neurology firmographics

Firmographics
Name
Eisai U.S. Neurology
Legal name
Eisai Inc.
Website
https://eisaineuro.com
Company type
Private
Operating status
Operating
Headcount range
51–100 employees
Short description
Eisai U.S. Neurology is the U.S. subsidiary of Japan's Eisai Co., Ltd., developing and commercializing neurology therapeutics primarily for early Alzheimer's Disease through its FDA-approved LEQEMBI franchise, serving patients via healthcare providers, pharmacies, and Magnolia patient support programs.
Ownership category
akta.pro rank

Eisai U.S. Neurology industry classification

Industry
Product category
Neurology Pharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Cognitive & Behavioral Neurology (Dementia/Memory Disorders) (HLAKAIAH)

Keywords

  • Neurology pharmaceuticals
  • Alzheimer's disease therapeutics
  • Monoclonal antibody treatments
  • Neurodegenerative disease drugs
  • Sleep disorder medications

Where Eisai U.S. Neurology is headquartered

Location

Headquarters

HQ city
Nutley
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Eisai U.S. Neurology business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Marketing or Sales, Personnel, Operations, Supply Chain

Distribution channels3 records

Marketing channels4 records

Eisai U.S. Neurology product offering

Product offering

Core offering

Eisai U.S. Neurology develops, manufactures, and markets FDA-approved pharmaceutical therapeutics for neurodegenerative conditions, with a primary focus on Alzheimer's disease. Its flagship product LEQEMBI (lecanemab-irmb) is an amyloid-targeting monoclonal antibody available in IV formulation and a newly approved subcutaneous injection (LEQEMBI IQLIK) for initiation dosing in early Alzheimer's disease. The company also pursues research across tau, neurodegeneration, immunodementia, and sleep-wake disorders (insomnia and narcolepsy).

Product overview

Eisai U.S. Neurology operates as a pharmaceutical company focused on neurodegenerative disease treatments, with LEQEMBI® (lecanemab-irmb) as its flagship FDA-approved product for early Alzheimer's disease. The portfolio includes the original IV formulation and the newly approved LEQEMBI IQLIK® subcutaneous injection for treatment initiation. The company also operates G2D2, a dedicated R&D facility in Cambridge, MA pursuing next-generation immunodementia therapeutics. Research areas include amyloid targeting, tau, neurodegeneration, sleep-wake disorders (insomnia and narcolepsy), and the broader dementia pipeline.

Differentiator

Problem solved

Functional benefit

Brands

  • LEQEMBI (lecanemab-irmb): FDA-approved treatment for early Alzheimer's disease, available as IV formulation and subcutaneous injection (IQLIK).

Products and services

  • LEQEMBI (lecanemab-irmb) Humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody that selectively binds to amyloid-beta (Aβ) protofibrils. FDA-approved for the treatment of early Alzheimer's Disease and administered intravenously. Indicated for healthcare providers and patients with early-stage Alzheimer's Disease.
  • LEQEMBI IQLIK (lecanemab-irmb) Subcutaneous Injection Subcutaneous injection formulation of lecanemab approved as an initiation dose for early Alzheimer's Disease, offering an alternative to IV administration through an autoinjector delivery system. Improves patient accessibility compared to intravenous infusion.

Quantifiable outcome

  • Over 75% of early Alzheimer's patients remained stable and nearly 7% improved over average 17 months of LEQEMBI treatment

Companies that use Eisai U.S. Neurology

Customer profile

Segments2 records

Ideal customer profiles2 records

Eisai U.S. Neurology technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Eisai U.S. Neurology partnerships and signals

Strategic signal

Scale indicators3 records

Recent moves6 records

Expansion highlights5 records

Eisai U.S. Neurology competitors and assessment

Company assessment

Direct peers

  • Biogen: Biogen is the co-developer of LEQEMBI and markets competing/successor AD therapies (Aduhelm legacy, pipeline assets) — directly overlapping in disease-modifying Alzheimer's neurology with shared commercial infrastructure.
  • Eli Lilly: Eli Lilly markets Kisunla (donanemab), a competing anti-amyloid antibody approved for early Alzheimer's Disease — directly competing with LEQEMBI in the same indication, prescriber base, and payer landscape.

Broad incumbents

  • Bristol Myers Squibb: BMS operates a broad neuroscience and specialty therapeutics franchise with growing CNS investment — a larger incumbent competing for neurology talent, payer attention, and acquisition targets in the AD space.
  • Roche: Roche developed gantenerumab for Alzheimer's and operates a broad neuroscience portfolio — overlapping with Eisai in CNS drug development but across a wider therapeutic footprint including oncology and rare disease.
  • AbbVie: AbbVie maintains a broad neuroscience and specialty CNS portfolio and has invested in neurodegeneration research — a larger incumbent competing for HCP mindshare and pipeline assets in CNS therapeutics.

Regional players

  • Otsuka Pharmaceutical: Otsuka is a Japanese-headquartered pharmaceutical peer with overlapping neurology/CNS focus (e.g., Abilify, CNS pipeline) — comparable therapeutic categories but operating primarily through different geographic channels and partner arrangements.

Emerging players

  • Cognition Therapeutics: Cognition Therapeutics is developing CT1812 for early Alzheimer's Disease, targeting the sigma-2 receptor — emerging neurology player with overlapping disease-modifying AD ambition but differentiated mechanism.
  • Prothena Corporation: Prothena is a clinical-stage biotech developing anti-amyloid and tau-targeted therapies for neurodegenerative diseases — directly comparable pipeline focus on AD/immunodementia mechanisms with Eisai's G2D2 and LEQEMBI franchise.
  • Sage Therapeutics: Sage Therapeutics develops CNS therapies including Zurzuvae (postpartum depression) and pipeline neurology assets — comparable CNS-focused biopharma targeting specialty neurology prescribers with overlapping patient access infrastructure.
  • Acumen Pharmaceuticals: Acumen Pharmaceuticals is developing sabirnetug, an anti-amyloid antibody for early Alzheimer's Disease — emerging competitor pursuing the same patient population and mechanism class as LEQEMBI.

Market position

Strengths4 records

Weaknesses1 record

Competitive moat5 records

Key risks5 records

Key highlights7 records

Customer concentration

Eisai U.S. Neurology social profiles

Digital presence

Eisai U.S. Neurology financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Eisai U.S. Neurology leadership team

Management profile

Number of profiles

Eisai U.S. Neurology funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Eisai U.S. Neurology M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Eisai U.S. Neurology

What does Eisai U.S. Neurology do?

Eisai U.S. Neurology develops, manufactures, and markets FDA-approved pharmaceutical therapeutics for neurodegenerative conditions, with a primary focus on Alzheimer's disease. Its flagship product LEQEMBI (lecanemab-irmb) is an amyloid-targeting monoclonal antibody available in IV formulation and a newly approved subcutaneous injection (LEQEMBI IQLIK) for initiation dosing in early Alzheimer's disease. The company also pursues research across tau, neurodegeneration, immunodementia, and sleep-wake disorders (insomnia and narcolepsy).

When was Eisai U.S. Neurology founded?

Eisai U.S. Neurology was founded in -1. It employs 51 to 100 people.

Where is Eisai U.S. Neurology based?

Eisai U.S. Neurology is headquartered in Nutley, United States, in the North America region.

Who are Eisai U.S. Neurology's main competitors?

Direct peers on record are Biogen and Eli Lilly. Broad incumbents are Bristol Myers Squibb, Roche and AbbVie. Otsuka Pharmaceutical is listed as a regional player. Emerging players are Cognition Therapeutics, Prothena Corporation, Sage Therapeutics and Acumen Pharmaceuticals.

Does Eisai U.S. Neurology have an API?

No public API is recorded for Eisai U.S. Neurology.

What industry is Eisai U.S. Neurology in?

Eisai U.S. Neurology's product category is Neurology Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 541714 and its SIC code is 2834.

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