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MITSUBISHI TANABE PHARMA AMERICA

Full company profile

uuid02ltpr9

Namestring
MITSUBISHI TANABE PHARMA AMERICA
Legal namestring
TANABE PHARMA AMERICA, INC.
Company typeenum
Private
Founded yearint
2016
Operating statusenum
Operating
Ownership categoryenum
akta.pro rankint
HeadquartersJersey City, United States
HQ citystring
Jersey City
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
neurodegenerative disease treatments, rare disease therapeutics, specialty pharmaceutical products, clinical stage pharmaceuticals, prescription drug development
Industry3 codes
1Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Rare Neurology & Neurodegenerative Disorder Therapies
CodeHLAIAIADPrimaryNo
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing32541
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals (Neurology / Rare Disease)
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Sales
TypeOne Time License
Description

Sale of prescription pharmaceutical products including RADICAVA ORS (edaravone) for ALS treatment, with revenue generated through specialty pharmacy distribution and healthcare provider prescriptions.

us.tanabe-pharma.com
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
Pricing details1 tier
1Prescription pharmaceutical products - pricing not publicly disclosed
ModelOtherBilling cadenceOther
Notes

Pharmaceutical products require prescription and are typically covered by insurance. Specific pricing varies by formulation, dosage, and insurance coverage.

us.tanabe-pharma.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Tanabe Pharma America develops and commercializes prescription pharmaceutical products for serious and debilitating diseases including ALS, Parkinson's disease, and rare disorders such as erythropoietic protoporphyria. Its commercial portfolio has centered on RADICAVA (edaravone) for ALS — available as an oral suspension (RADICAVA ORS) and previously as an IV formulation — while its investigational pipeline includes ND0612 subcutaneous infusion for Parkinson's disease, dersimelagon for EPP/XLP, and oncology and spinal cord injury assets.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 33% slowing of physical function loss in ALS patients vs placebo in pivotal Phase 3 trial
+2 more records
Product overview1 text field

Tanabe Pharma America (formerly Mitsubishi Tanabe Pharma America) is a U.S. pharmaceutical company and wholly-owned subsidiary of Tanabe Pharma Corporation, focused on developing and commercializing treatments for serious and debilitating diseases. Its commercial portfolio historically centered on RADICAVA (edaravone), the first new FDA-approved ALS treatment in over two decades, available in both IV (RADICAVA IV, discontinued April 2025) and oral suspension (RADICAVA ORS) formulations. The company also commercialized EXSERVAN (riluzole) oral film for ALS, discontinued September 2024. The investigational pipeline includes ND0612 (24-hour subcutaneous levodopa/carbidopa infusion for Parkinson's disease, NDA under FDA review), dersimelagon/MT-7117 (selective MC1R agonist for EPP and XLP porphyrias, Phase 3 completed with positive results), MT-3921 (anti-RGMa monoclonal antibody for spinal cord injury), and MT-4561 (oncology, first patient dosed 2025). The RADICAVA business was transferred to Shionogi Inc. in April 2026. The company maintains patient support services including Searchlight Support and the JourneyMate nurse education program.

Product and service7 records
1RADICAVA ORS (edaravone oral suspension)
CategoryPrescription pharmaceutical product (ALS)
Description

FDA-approved oral suspension formulation of edaravone (105 mg/5 mL) for the treatment of amyotrophic lateral sclerosis (ALS). Taken daily for 14 consecutive days followed by a 14-day drug-free period for the initial cycle, then 10 days within a 14-day period for subsequent cycles. Currently prescribed to more than 4,000 patients as of October 2024.

2ND0612 (continuous subcutaneous levodopa/carbidopa infusion)
CategoryInvestigational pharmaceutical product (Parkinson's disease)
Description

Investigational 24-hour continuous subcutaneous infusion of levodopa/carbidopa for Parkinson's disease. Developed by NeuroDerm, Ltd. Subject of the pivotal Phase 3 BouNDless trial and its open-label extension.

3Dersimelagon (MT-7117)
CategoryInvestigational pharmaceutical product (rare porphyrias)
Description

Investigational novel synthetic, orally-administered, non-peptide small molecule selective melanocortin-1 receptor (MC1R) agonist in development for erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP).

4MT-3921
CategoryInvestigational pharmaceutical product (spinal cord injury)
Description

Investigational anti-RGMa (repulsive guidance molecule A) inhibition monoclonal antibody in development for spinal cord injury treatment, targeting a distinct pathophysiological pathway.

5MT-4561
CategoryInvestigational pharmaceutical product (oncology)
Description

Investigational oncology asset for advanced solid tumors; first patient dosed June 2025.

6Searchlight Support
CategoryPatient support service
Description

Patient support program offered by Tanabe Pharma America to assist patients and caregivers with access, reimbursement, and navigation support for the company's therapies.

7JourneyMate Program
CategoryPatient support service
Description

Live nurse educational phone support program for ALS patients and caregivers, part of the company's patient support ecosystem.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership12 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-22
Description

Transfer of global rights to RADICAVA (edaravone) including rights in Japan, United States, and Canada to Shionogi. Transaction finalized April 1, 2026 to support long-term growth and sustainability of the brand.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2024-12-17
Description

Research collaboration between Mitsubishi Tanabe Pharma Corporation and Dewpoint Therapeutics to advance small molecule condensate modulator for ALS.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2024-09-04
Description

AI collaboration completed to further understanding of autism spectrum disorder.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2021-06-25
Description

Exclusive specialty pharmacy provider for EXSERVAN (riluzole oral film). Partnership ended with product discontinuation.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2021-03-03
Description

Partnership to collect real-world data in ALS with the goal of improving patient care.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-01-21
Description

Licensing and supply deal for riluzole oral film (EXSERVAN) using Aquestive's PharmFilm drug delivery technology. MTPA commercialized in U.S.; Aquestive served as exclusive sole manufacturer and supplier. Product discontinued September 2024.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2019-05-03
Description

Joined ALS biomarker study sponsored by Mitsubishi Tanabe Pharma America.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2019-03-28
Description

Collaboration on ALS biomarker study.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2017-09-06
Description

National home infusion services agreement for RADICAVA IV. Partnership ended with IV product discontinuation.

Strategic tierStrategicTypeGTM or Marketing PartnerAnnounced on2016-09-20
Description

National corporate sponsorship of Walk to Defeat ALS and care service programs. Partnership for ALS awareness, research funding, and advocacy efforts.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

NeuroDerm, Ltd. is a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation leading development of ND0612, a 24-hour continuous subcutaneous levodopa/carbidopa infusion for Parkinson's disease.

Strategic tierMinorTypeGTM or Marketing Partner
Description

UPA provides recruitment information for INSPIRE clinical study of dersimelagon for EPP and XLP patients.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

UCB is a global biopharma with a strong neurology and rare disease portfolio (including epilepsy and myasthenia gravis treatments). They operate as a broad incumbent in the same neurology specialty channels and compete for the same specialist prescribers.

TypeDirect peer
Description

BioMarin is a rare disease specialty pharmaceutical company with multiple orphan drug products. Both companies focus on rare disease commercialization, orphan drug exclusivity strategies, and high-priced specialty therapeutics targeting limited patient populations.

TypeDirect peer
Description

Amylyx is a direct ALS competitor (maker of AMX0035/relyvrio, now discontinued but with follow-on pipeline). Both companies have ALS as a core indication and target the same specialist neurology prescribers with orphan drug pricing strategies.

TypeDirect peer
Description

Supernus is a specialty pharma company focused on CNS disorders, with a similar profile of differentiated formulations of established molecules and a focus on neurology specialists. Both companies employ specialty pharmacy distribution and target rare neurology indications.

TypeDirect peer
Description

Sage Therapeutics is a CNS-focused pharmaceutical company developing treatments for neurological disorders. They share the same late-stage clinical, regulatory, and commercialization playbook for CNS drugs targeting limited patient populations.

TypeEmerging player
Description

Alnylam is an emerging player in rare disease therapeutics with a strong pipeline of orphan drug products. Both companies target rare hereditary disorders with high unmet need and use orphan drug designation and premium pricing strategies.

TypeDirect peer
Description

Cytokinetics is a direct peer in ALS drug development (relyvrio was previously approved; their cardiac myosin activator is in development). Both companies target rare neuromuscular diseases with high unmet need and rely on specialist neurology channels and orphan drug pricing strategies.

TypeBroad incumbent
Description

Jazz Pharmaceuticals is a specialty pharma with rare neurological disease products (including Xywav, Epidiolex). They share the specialty pharmacy distribution model and rare disease orphan drug commercialization playbook with Tanabe Pharma America.

TypeDirect peer
Description

Recordati Rare Diseases is a specialty pharmaceutical company focused on rare disease treatments. Both companies share the orphan drug business model, specialty distribution approach, and focus on small patient populations with limited treatment options.

TypeDirect peer
Description

Biogen is the most direct peer — a major CNS/neurology pharmaceutical company with multiple ALS treatments (including Qalsody) and a strong Parkinson's disease and rare disease portfolio. Both companies compete in the U.S. neurology specialist prescriber market with similar HCP targeting and specialty pharmacy distribution models.

Market position
Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

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

Ideal customer profile3 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance6 records

Each record includes

Name, Class, Description

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 →

MITSUBISHI TANABE PHARMA AMERICA

Specialty Pharmaceuticals (Neurology / Rare Disease)mt-pharma-america.com

MITSUBISHI TANABE PHARMA AMERICA firmographics

Firmographics
Name
MITSUBISHI TANABE PHARMA AMERICA
Legal name
TANABE PHARMA AMERICA, INC.
Website
https://mt-pharma-america.com
Company type
Private
Founded year
2016
Operating status
Operating
Ownership category
akta.pro rank

MITSUBISHI TANABE PHARMA AMERICA industry classification

Industry
Product category
Specialty Pharmaceuticals (Neurology / Rare Disease)
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (32541)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Rare Neurology & Neurodegenerative Disorder Therapies (HLAIAIAD)

Keywords

  • Neurodegenerative disease treatments
  • Rare disease therapeutics
  • Specialty pharmaceutical products
  • Clinical stage pharmaceuticals
  • Prescription drug development

Where MITSUBISHI TANABE PHARMA AMERICA is headquartered

Location

Headquarters

HQ city
Jersey City
HQ country
United States
HQ region
North America

Offices2 records

Markets served

MITSUBISHI TANABE PHARMA AMERICA 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

Revenue model

  1. Pharmaceutical Product Sales: Sale of prescription pharmaceutical products including RADICAVA ORS (edaravone) for ALS treatment, with revenue generated through specialty pharmacy distribution and healthcare provider prescriptions.

Pricing tiers

ModelBillingPrice
OtherOtherPrescription pharmaceutical products - pricing not publicly disclosed

Go-to-market motion1 record

Distribution channels3 records

Marketing channels4 records

MITSUBISHI TANABE PHARMA AMERICA product offering

Product offering

Core offering

Tanabe Pharma America develops and commercializes prescription pharmaceutical products for serious and debilitating diseases including ALS, Parkinson's disease, and rare disorders such as erythropoietic protoporphyria. Its commercial portfolio has centered on RADICAVA (edaravone) for ALS — available as an oral suspension (RADICAVA ORS) and previously as an IV formulation — while its investigational pipeline includes ND0612 subcutaneous infusion for Parkinson's disease, dersimelagon for EPP/XLP, and oncology and spinal cord injury assets.

Product overview

Tanabe Pharma America (formerly Mitsubishi Tanabe Pharma America) is a U.S. pharmaceutical company and wholly-owned subsidiary of Tanabe Pharma Corporation, focused on developing and commercializing treatments for serious and debilitating diseases. Its commercial portfolio historically centered on RADICAVA (edaravone), the first new FDA-approved ALS treatment in over two decades, available in both IV (RADICAVA IV, discontinued April 2025) and oral suspension (RADICAVA ORS) formulations. The company also commercialized EXSERVAN (riluzole) oral film for ALS, discontinued September 2024. The investigational pipeline includes ND0612 (24-hour subcutaneous levodopa/carbidopa infusion for Parkinson's disease, NDA under FDA review), dersimelagon/MT-7117 (selective MC1R agonist for EPP and XLP porphyrias, Phase 3 completed with positive results), MT-3921 (anti-RGMa monoclonal antibody for spinal cord injury), and MT-4561 (oncology, first patient dosed 2025). The RADICAVA business was transferred to Shionogi Inc. in April 2026. The company maintains patient support services including Searchlight Support and the JourneyMate nurse education program.

Differentiator

Problem solved

Functional benefit

Products and services

  • RADICAVA ORS (edaravone oral suspension) FDA-approved oral suspension formulation of edaravone (105 mg/5 mL) for the treatment of amyotrophic lateral sclerosis (ALS). Taken daily for 14 consecutive days followed by a 14-day drug-free period for the initial cycle, then 10 days within a 14-day period for subsequent cycles. Currently prescribed to more than 4,000 patients as of October 2024.
  • ND0612 (continuous subcutaneous levodopa/carbidopa infusion) Investigational 24-hour continuous subcutaneous infusion of levodopa/carbidopa for Parkinson's disease. Developed by NeuroDerm, Ltd. Subject of the pivotal Phase 3 BouNDless trial and its open-label extension.
  • Dersimelagon (MT-7117) Investigational novel synthetic, orally-administered, non-peptide small molecule selective melanocortin-1 receptor (MC1R) agonist in development for erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP).
  • MT-3921 Investigational anti-RGMa (repulsive guidance molecule A) inhibition monoclonal antibody in development for spinal cord injury treatment, targeting a distinct pathophysiological pathway.
  • MT-4561 Investigational oncology asset for advanced solid tumors; first patient dosed June 2025.
  • Searchlight Support Patient support program offered by Tanabe Pharma America to assist patients and caregivers with access, reimbursement, and navigation support for the company's therapies.
  • JourneyMate Program Live nurse educational phone support program for ALS patients and caregivers, part of the company's patient support ecosystem.

Quantifiable outcome

  • 33% slowing of physical function loss in ALS patients vs placebo in pivotal Phase 3 trial
  • +2 more outcomes

Companies that use MITSUBISHI TANABE PHARMA AMERICA

Customer profile

Named customers3 records

Segments3 records

Ideal customer profiles3 records

MITSUBISHI TANABE PHARMA AMERICA technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

MITSUBISHI TANABE PHARMA AMERICA partnerships and signals

Strategic signal

Partnerships

Twelve partnerships are on record, tiered core, strategic and minor.

  • Shionogi Inc.coreStrategic or Co-development Partner · 22 December 2025Transfer of global rights to RADICAVA (edaravone) including rights in Japan, United States, and Canada to Shionogi. Transaction finalized April 1, 2026 to support long-term growth and sustainability of the brand.
  • Dewpoint TherapeuticsstrategicStrategic or Co-development Partner · 17 December 2024Research collaboration between Mitsubishi Tanabe Pharma Corporation and Dewpoint Therapeutics to advance small molecule condensate modulator for ALS.
  • Nobias TherapeuticsminorStrategic or Co-development Partner · 4 September 2024AI collaboration completed to further understanding of autism spectrum disorder.
  • PANTHERxcoreChannel Partner/ Reseller/ Distributor · 25 June 2021Exclusive specialty pharmacy provider for EXSERVAN (riluzole oral film). Partnership ended with product discontinuation.
  • ALS/MND Natural History Study ConsortiumstrategicStrategic or Co-development Partner · 3 March 2021Partnership to collect real-world data in ALS with the goal of improving patient care.
  • Aquestive TherapeuticscoreOEM/ Whitelabel/ Licensing Partner · 21 January 2021Licensing and supply deal for riluzole oral film (EXSERVAN) using Aquestive's PharmFilm drug delivery technology. MTPA commercialized in U.S.; Aquestive served as exclusive sole manufacturer and supplier. Product discontinued September 2024.
  • Oxford BiodynamicsminorStrategic or Co-development Partner · 3 May 2019Joined ALS biomarker study sponsored by Mitsubishi Tanabe Pharma America.
  • Massachusetts General HospitalstrategicStrategic or Co-development Partner · 28 March 2019Collaboration on ALS biomarker study.
  • Option CarecoreChannel Partner/ Reseller/ Distributor · 6 September 2017National home infusion services agreement for RADICAVA IV. Partnership ended with IV product discontinuation.
  • ALS AssociationstrategicGTM or Marketing Partner · 20 September 2016National corporate sponsorship of Walk to Defeat ALS and care service programs. Partnership for ALS awareness, research funding, and advocacy efforts.
  • NeuroDerm, Ltd.coreStrategic or Co-development PartnerNeuroDerm, Ltd. is a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation leading development of ND0612, a 24-hour continuous subcutaneous levodopa/carbidopa infusion for Parkinson's disease.
  • United Porphyrias AssociationminorGTM or Marketing PartnerUPA provides recruitment information for INSPIRE clinical study of dersimelagon for EPP and XLP patients.

Scale indicators3 records

Recent moves7 records

Expansion highlights5 records

MITSUBISHI TANABE PHARMA AMERICA competitors and assessment

Company assessment

Broad incumbents

  • UCB: UCB is a global biopharma with a strong neurology and rare disease portfolio (including epilepsy and myasthenia gravis treatments). They operate as a broad incumbent in the same neurology specialty channels and compete for the same specialist prescribers.
  • Jazz Pharmaceuticals: Jazz Pharmaceuticals is a specialty pharma with rare neurological disease products (including Xywav, Epidiolex). They share the specialty pharmacy distribution model and rare disease orphan drug commercialization playbook with Tanabe Pharma America.

Direct peers

  • BioMarin Pharmaceutical: BioMarin is a rare disease specialty pharmaceutical company with multiple orphan drug products. Both companies focus on rare disease commercialization, orphan drug exclusivity strategies, and high-priced specialty therapeutics targeting limited patient populations.
  • Amylyx Pharmaceuticals: Amylyx is a direct ALS competitor (maker of AMX0035/relyvrio, now discontinued but with follow-on pipeline). Both companies have ALS as a core indication and target the same specialist neurology prescribers with orphan drug pricing strategies.
  • Supernus Pharmaceuticals: Supernus is a specialty pharma company focused on CNS disorders, with a similar profile of differentiated formulations of established molecules and a focus on neurology specialists. Both companies employ specialty pharmacy distribution and target rare neurology indications.
  • Sage Therapeutics: Sage Therapeutics is a CNS-focused pharmaceutical company developing treatments for neurological disorders. They share the same late-stage clinical, regulatory, and commercialization playbook for CNS drugs targeting limited patient populations.
  • Cytokinetics: Cytokinetics is a direct peer in ALS drug development (relyvrio was previously approved; their cardiac myosin activator is in development). Both companies target rare neuromuscular diseases with high unmet need and rely on specialist neurology channels and orphan drug pricing strategies.
  • Recordati Rare Diseases: Recordati Rare Diseases is a specialty pharmaceutical company focused on rare disease treatments. Both companies share the orphan drug business model, specialty distribution approach, and focus on small patient populations with limited treatment options.
  • Biogen: Biogen is the most direct peer — a major CNS/neurology pharmaceutical company with multiple ALS treatments (including Qalsody) and a strong Parkinson's disease and rare disease portfolio. Both companies compete in the U.S. neurology specialist prescriber market with similar HCP targeting and specialty pharmacy distribution models.

Emerging players

  • Alnylam Pharmaceuticals: Alnylam is an emerging player in rare disease therapeutics with a strong pipeline of orphan drug products. Both companies target rare hereditary disorders with high unmet need and use orphan drug designation and premium pricing strategies.

Market position

Weaknesses4 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

MITSUBISHI TANABE PHARMA AMERICA social profiles

Digital presence

MITSUBISHI TANABE PHARMA AMERICA compliance and trust

Trust signal

Compliance6 records

MITSUBISHI TANABE PHARMA AMERICA financial estimates

Financial estimate

Revenue estimate

Valuation estimate

MITSUBISHI TANABE PHARMA AMERICA leadership team

Management profile

Number of profiles

Profiles3 records

MITSUBISHI TANABE PHARMA AMERICA subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

MITSUBISHI TANABE PHARMA AMERICA funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

MITSUBISHI TANABE PHARMA AMERICA 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 MITSUBISHI TANABE PHARMA AMERICA

What does MITSUBISHI TANABE PHARMA AMERICA do?

Tanabe Pharma America develops and commercializes prescription pharmaceutical products for serious and debilitating diseases including ALS, Parkinson's disease, and rare disorders such as erythropoietic protoporphyria. Its commercial portfolio has centered on RADICAVA (edaravone) for ALS — available as an oral suspension (RADICAVA ORS) and previously as an IV formulation — while its investigational pipeline includes ND0612 subcutaneous infusion for Parkinson's disease, dersimelagon for EPP/XLP, and oncology and spinal cord injury assets.

Is MITSUBISHI TANABE PHARMA AMERICA a public or private company?

MITSUBISHI TANABE PHARMA AMERICA is a private company. It is classified as corporate owned and is currently operating.

When was MITSUBISHI TANABE PHARMA AMERICA founded?

MITSUBISHI TANABE PHARMA AMERICA was founded in 2016.

Where is MITSUBISHI TANABE PHARMA AMERICA based?

MITSUBISHI TANABE PHARMA AMERICA is headquartered in Jersey City, United States, in the North America region.

How does MITSUBISHI TANABE PHARMA AMERICA make money?

One revenue line is on record: pharmaceutical Product Sales.

Who are MITSUBISHI TANABE PHARMA AMERICA's main competitors?

Broad incumbents on record are UCB and Jazz Pharmaceuticals. Direct peers are BioMarin Pharmaceutical, Amylyx Pharmaceuticals, Supernus Pharmaceuticals, Sage Therapeutics, Cytokinetics, Recordati Rare Diseases and Biogen. Alnylam Pharmaceuticals is listed as an emerging player.

Does MITSUBISHI TANABE PHARMA AMERICA have an API?

No public API is recorded for MITSUBISHI TANABE PHARMA AMERICA.

What industry is MITSUBISHI TANABE PHARMA AMERICA in?

MITSUBISHI TANABE PHARMA AMERICA's product category is Specialty Pharmaceuticals (Neurology / Rare Disease). 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 325412 and its SIC code is 2834.

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Live signals
PR NewswireMitsubishi Tanabe Pharma America to Present New Data on Investigational ND0612 at the 2025 International Congress of Parkinson's Disease and Movement Disorders®Mitsubishi Tanabe Pharma America announced four poster presentations on investigational ND0612 for Parkinson's disease will be shared at the 2025 International Congress of Parkinson's Disease and Movement Disorders® in Honolulu, Hawaii. The presentations will share findings from the pivotal Phase 3 BouNDless study, which evaluated continuous subcutaneous levodopa/carbidopa infusion against standard of care in patients experiencing motor fluctuations. Development of ND0612 is being led by NeuroDerm, Ltd., a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation.PR NewswireMitsubishi Tanabe Pharma America to Share Latest Data on Investigational ND0612 at the 2025 International Conference on Alzheimer's and Parkinson's Diseases (AD/PD)Mitsubishi Tanabe Pharma America announced it will present three poster presentations on investigational ND0612, a 24-hour continuous subcutaneous infusion of levodopa/carbidopa for Parkinson's disease, at the 2025 International Conference on Alzheimer's and Parkinson's Diseases in Vienna, Austria. The presentations will share findings from the pivotal Phase 3 BouNDless trial and its open-label extension phase, including subgroup analyses on efficacy and safety, one-year outcomes, and quality-of-life data from patients with motor fluctuations. Development of ND0612 is led by NeuroDerm, Ltd., a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation.PR NewswireMitsubishi Tanabe Pharma America, Inc. (MTPA) Stands with the ALS CommunityMitsubishi Tanabe Pharma America, Inc. (MTPA) is reaffirming its commitment to the amyotrophic lateral sclerosis (ALS) community in light of recent challenges affecting ALS treatments. The company emphasizes its focus on research and support, highlighting that over 14,600 people in the U.S. have been treated with RADICAVA and RADICAVA ORS since their approval, demonstrating the products' effectiveness in slowing the decline of physical function in ALS patients. MTPA continues to evaluate the ongoing potential of these treatments while gathering real-world evidence to enhance their understanding and support of ALS.PR NewswireMitsubishi Tanabe Pharma America Announces Presentations at XXIX World Congress on Parkinson's Disease and Related DisordersThe posters cover the Phase 3 BouNDless trial and three-year outcomes from the Phase 2b BeyoND study. ND0612 is a continuous subcutaneous levodopa/carbidopa infusion developed by NeuroDerm, a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation.PR NewswireMitsubishi Tanabe Pharma America Celebrates Eight-Year Anniversary in the U.S.Mitsubishi Tanabe Pharma America (MTPA) is celebrating its eight-year anniversary in the U.S., highlighting the commercial success of its ALS treatment RADICAVA and RADICAVA ORS, which have been prescribed to over 14,600 patients. The company also noted recent organizational integration with its development entities and ongoing regulatory recognition, including FDA-granted Orphan Drug Exclusivity for the oral formulation.PR NewswireMitsubishi Tanabe Pharma America to Showcase Breadth of Neurodegenerative Research at 2024 American Academy of Neurology Annual MeetingMitsubishi Tanabe Pharma America (MTPA) announced it will present seven abstracts at the American Academy of Neurology 2024 Annual Meeting in Denver, Colorado from April 13-18, covering Parkinson's disease and ALS research. The presentations include Phase 3 BouNDless trial subgroup analyses for investigational ND0612 in PD and real-world findings from RADICAVA (edaravone) treatment in ALS patients. ND0612, developed by NeuroDerm under MTPC, has a PDUFA target action date in Q2 2024 for treating motor fluctuations in PD patients.PR NewswireSpinal Cord Injury Market Likely to Exhibit Substantial Growth by 2032, Assesses DelveInsight | Companies to Watch Out - NervGen Pharma, StemCyte, Mitsubishi Tanabe Pharma America, AbbVieDelveInsight released a market report forecasting substantial growth in the spinal cord injury market through 2032, driven by improved diagnostics and emerging therapies. The analysis highlights key industry players including NervGen Pharma, StemCyte, Mitsubishi Tanabe Pharma America, and AbbVie who are developing novel treatments for the condition.GlobeNewswireMuscular Dystrophy Association Announces Collaboration with Mitsubishi Tanabe Pharma America for Remote Digital Technology Research Study for Amyotrophic Lateral Sclerosis (ALS)MDA and Mitsubishi Tanabe Pharma America announced a remote ALS study, ALS Go-Digital, recruiting 75 participants from MOVR's 2,000 enrolled patients. The study uses Fitbit, a smartphone app, and an eCOA platform to track progression over one year, aiming to validate remote data collection for clinical trials.PR NewswireMitsubishi Tanabe Pharma America Spotlights ALS Research at the XXVI World Congress of NeurologyThe presentations cover real-world data on intravenous edaravone, oral edaravone dosing regimens, and 48-week safety results. The company reported RADICAVA and RADICAVA ORS have treated over 12,000 U.S. patients.PR NewswireMitsubishi Tanabe Pharma America Presents Positive Results from Pivotal Phase 3 BouNDless Trial of Investigational ND0612 in People with Parkinson's Disease Experiencing Motor FluctuationsMitsubishi Tanabe Pharma America presented positive results from the pivotal Phase 3 BouNDless trial of investigational ND0612, a 24-hour continuous subcutaneous infusion of levodopa/carbidopa for Parkinson's disease, at the International Congress of Parkinson's Disease and Movement Disorder Society in Copenhagen, Denmark. The trial met its primary endpoint with a statistically significant increase of 1.72 hours in 'ON' time without troublesome dyskinesia compared to oral levodopa/carbidopa, and also achieved the first four secondary endpoints. Development of ND0612 is led by NeuroDerm, Ltd., a wholly-owned subsidiary of Mitsubishi Tanabe Pharma Corporation, with MTPA intending to commercialize the therapy in the U.S. upon regulatory approval.