Seqens Seqens

X
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Syndrome","therapeuticArea":"Neurology","highestDevelopmentStatus":"Phase II","country":"U.S.A","productType":"Small molecule","productStatus":"Approved","date":"April 2024","url1":"","url2":"","graph1":"Neurology","graph2":"Phase II"}]

Find Clinical Drug Pipeline Developments & Deals for Sodium 4-Phenylbutyrate

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            Details:

            The net proceeds will be used for launching Olpruva, a new formulation of sodium phenylbutyrate approved as an oral suspension by the FDA, to treat patients with urea cycle disorders.

            Lead Product(s): Sodium Phenylbutyrate

            Therapeutic Area: Genetic Disease Product Name: Olpruva

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Perceptive Advisors

            Deal Size: Undisclosed Upfront Cash: Undisclosed

            Deal Type: Financing April 10, 2024

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            Details:

            Relyvrio (taurursodiol and sodium phenylbutyrate) is a glutamine chelator small molecule drug candidate, available in the form of oral powder in sachet. It is currently being evaluated for the treatment of wolfram syndrome.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: Relyvrio

            Highest Development Status: Phase II Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable April 10, 2024

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            Relyvrio (sodium phenylbutyrate and taurursodiol) is an oral fixed-dose medication, indicated for the treatment amyotrophic lateral sclerosis, it is currently in discussion with FDA & Health Canada for voluntarily discontinuation of its marketing authorizations.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: Relyvrio

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable April 05, 2024

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            Details:

            Relyvrio (sodium phenylbutyrate and taurursodiol) is a specially formulated oral fixed-dose combination, which is being evaluated for the treatment of Amyotrophic Lateral Sclerosis.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: Relyvrio

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable March 08, 2024

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            Details:

            Relyvrio (sodium phenylbutyrate and taurursodiol) is an oral, fixed-dose combination. It is a HDAC inhibitor which is being evaluated in phase 2 clinical trials for the treatment of Wolfram syndrome.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Rare Diseases and Disorders Product Name: Relyvrio

            Highest Development Status: Phase II Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable February 08, 2024

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            Details:

            Amylyx investigational product Relyvrio (sodium phenylbutyrate) with Taurursodiol, is an oral, fixed-dose combination therapy. It is being evaluated in the Phase III clinical trial studies with patient for the treatment of Progressive Supranuclear Palsy.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: Relyvrio

            Highest Development Status: Phase III Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable December 22, 2023

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            Details:

            Through the acquisition, Zevra will expand its rare disease portfolio and adding commercial product including the recent U.S. commercial approval Olpruva (sodium phenylbutyrate) for the treatment of urea cycle disorders.

            Lead Product(s): Sodium Phenylbutyrate

            Therapeutic Area: Genetic Disease Product Name: Olpruva

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Zevra Therapeutics

            Deal Size: Undisclosed Upfront Cash: Undisclosed

            Deal Type: Acquisition November 20, 2023

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            Details:

            AMX0035 (sodium phenylbutyrate and ursodoxicoltaurine [also known as taurursodiol]), under the trade name Albrioza, received negative opinion from CHMP, for the treatment of amyotrophic lateral sclerosis (ALS).

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: AMX0035

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable October 13, 2023

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            Details:

            Albrioza (sodium phenylbutyrate and taurursodiol) is an oral fixed-dose medication approved with conditions to treat amyotrophic lateral sclerosis (ALS) currently being indicated for the treatment of amyotrophic lateral sclerosis.

            Lead Product(s): Sodium Phenylbutyrate,Tauroursodeoxycholic Acid

            Therapeutic Area: Neurology Product Name: Relyvrio

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable October 05, 2023

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            Details:

            Through the acquisition, Zevra will expand its rare disease portfolio and adding commercial product including the recent U.S. commercial approval Olpruva (sodium phenylbutyrate) for the treatment of UCDs.

            Lead Product(s): Sodium Phenylbutyrate

            Therapeutic Area: Genetic Disease Product Name: Olpruva

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Zevra Therapeutics

            Deal Size: Undisclosed Upfront Cash: Undisclosed

            Deal Type: Acquisition August 31, 2023

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