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Acorda Therapeutics
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420 Saw Mill River Road, Ardsley, NY United States 10502
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1-800-367-5109
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Merz Therapeutics will purchase substantially all of the assets of Acorda, including the rights to Inbrija (levodopa inhalation powder), Ampyra (dalfampridine), and Fampyra (dalfampridine). INBRIJA is used when needed for OFF episodes in adults with Parkinson's disease.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merz Pharma

Deal Size: $185.0 million Upfront Cash: Undisclosed

Deal Type: Acquisition April 02, 2024

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Under the termination, Acorda will regain global commercialization rights to Fampyra, a prolonged-release tablet formulation of the drug fampridine (4-aminopyridine, 4-AP or dalfampridine) for adult patients with multiple sclerosis with walking disability.


Lead Product(s): Fampridine

Therapeutic Area: Neurology Product Name: Fampyra

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Biogen

Deal Size: $510.0 million Upfront Cash: $110.0 million

Deal Type: Termination January 11, 2024

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INBRIJA® (levodopa) is approved for intermittent treatment of OFF episodes in adults with Parkinson’s disease treated with carbidopa. INBRIJA utilizes ARCUS® pulmonary delivery system, a technology platform designed to deliver medication through inhalation.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 06, 2023

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The collaboration aims to provide INBRIJA® in China. Inbrija (levodopa) is indicated in the United States for the intermittent treatment of episodic motor fluctuations in adult patients with Parkinson's disease treated with a levodopa/dopa-decarboxylase inhibitor.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Chance Pharmaceuticals

Deal Size: $144.0 million Upfront Cash: $2.5 million

Deal Type: Agreement May 08, 2023

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Inbrija (levodopa) is levodopa/dopa-decarboxylase inhibitor, it is converted to dopamine replacement agent for the intermittent treatment of episodic motor fluctuations of Parkinson disease.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Esteve Quimica

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 07, 2023

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INBRIJA® (levodopa) is approved for intermittent treatment of OFF episodes in adults with Parkinson’s disease treated with carbidopa. INBRIJA utilizes ARCUS® pulmonary delivery system, a technology platform designed to deliver medication through inhalation.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Catalent Pharma Solutions

Deal Size: $10.0 million Upfront Cash: Undisclosed

Deal Type: Agreement January 05, 2023

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SYN117 (nepicastat), is a small molecule drug and the license agreement provides for its development for all non-psychiatric indications and therapeutic uses. The asset has been held by Acorda’s U.S. subsidiary, Biotie Therapies, Inc.


Lead Product(s): Nepicastat

Therapeutic Area: Neurology Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Asieris Pharmaceuticals

Deal Size: $7.5 million Upfront Cash: $0.5 million

Deal Type: Licensing Agreement August 29, 2022

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INBRIJA® 33 mg (levodopa inhalation powder, hard capsules) is indicated in the EU for the intermittent treatment of episodic motor uctuations (OFF episodes) in adult patients with Parkinson’s disease treated with a levodopa/dopa-decarboxylase inhibitor.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Esteve Huayi Pharmaceutical

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement June 16, 2022

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Under the terms of the agreements, Acorda will receive a significant percentage of the selling price of INBRIJA in Latin America in exchange for supply of the product. Biopas plans on seeking marketing authorization in all countries to make Inbrija available for patients.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Biopas Laboratories

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement May 11, 2022

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Under the agreement, ESTEVE will have the exclusive distribution rights to INBRIJA in Germany and ACORDA will supply the product to ESTEVE. ESTEVE expects to launch INBRIJA in Germany by mid-2022.


Lead Product(s): Etilevodopa

Therapeutic Area: Neurology Product Name: Inbrija

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Esteve Huayi Pharmaceutical

Deal Size: Undisclosed Upfront Cash: $5.6 million

Deal Type: Agreement November 09, 2021

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