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AMO Pharma
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Kemp House, 152-160 City Road, London, EC1V 2NX
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+44 (0) 1483 319070
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Details:

The collaboration aims to support clinical proof of concept trial to assess the efficacy of AMO-02 (tideglusib), AMO investigational oral glycogen synthase kinase 3 beta (GSK3β) inhibitor, which is used in the treatment of genotype positive arrhythmogenic cardiomyopathy.


Lead Product(s): Tideglusib

Therapeutic Area: Cardiology/Vascular Diseases Product Name: AMO-02

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Population Health Research Institute

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration February 15, 2024

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AMO-02 (tideglusib), has a dual mechanism disrupting the pathogenic RNA repeat in CDM1 and inhibiting excess levels of the kinase GSK3β. It is in development for the treatment of congenital myotonic dystrophy.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: AMO-02

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 19, 2023

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AMO-02 (tideglusib), has a dual mechanism disrupting the pathogenic RNA repeat in CDM1 and inhibiting excess levels of the kinase GSK3β. It is in development for the treatment of congenital myotonic dystrophy.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: AMO-02

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 25, 2023

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Details:

AMO-02 (tideglusib), has a dual mechanism disrupting the pathogenic RNA repeat in CDM1 and inhibiting excess levels of the kinase GSK3β. It is in development for the treatment of congenital myotonic dystrophy.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: AMO-02

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 27, 2023

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AMO-02 (tideglusib) is in development for the treatment of congenital myotonic dystrophy and has potential for use in adult-onset myotonic dystrophy, additional CNS, neuromuscular and other orphan indications.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: AMO-02

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 05, 2022

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Designation qualifies AMO-02 for fast track review and AMO Pharma to receive a priority review voucher pending marketing approval. AMO-02, AMO-01 and AMO-04 are investigational medicines that have not yet been approved for the treatment of patients anywhere in the world.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: AMO-02

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 09, 2020

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Trial to assess AMO-02 in treatment of congenital myotonic dystrophy to begin patient enrollment in early 2020.


Lead Product(s): Tideglusib

Therapeutic Area: Genetic Disease Product Name: Undisclosed

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 09, 2020

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