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Muscular Atrophy Articles & Analysis

9 news found

Sage Therapeutics and Biogen Present Further Analyses from Phase 3 SKYLARK Study of Zuranolone in Postpartum Depression at the European College of Neuropsychopharmacology (ECNP) Congress

Sage Therapeutics and Biogen Present Further Analyses from Phase 3 SKYLARK Study of Zuranolone in Postpartum Depression at the European College of Neuropsychopharmacology (ECNP) Congress

Today, Biogen has a leading portfolio of medicines to treat multiple sclerosis, has introduced the first approved treatment for spinal muscular atrophy, and developed the first and only approved treatment to address a defining pathology of Alzheimer’s disease. ...

BySage Therapeutics


Sage Therapeutics and Biogen to Host Investor Webcast on December 6, 2022 to Discuss Potential Commercialization Plans for Zuranolone

Sage Therapeutics and Biogen to Host Investor Webcast on December 6, 2022 to Discuss Potential Commercialization Plans for Zuranolone

Today, Biogen has a leading portfolio of medicines to treat multiple sclerosis, has introduced the first approved treatment for spinal muscular atrophy, and developed the first and only approved treatment to address a defining pathology of Alzheimer’s disease. ...

BySage Therapeutics


Sage Therapeutics and Biogen Present New Analyses at Psych Congress Further Evaluating the Efficacy and Safety of Zuranolone

Sage Therapeutics and Biogen Present New Analyses at Psych Congress Further Evaluating the Efficacy and Safety of Zuranolone

Today, Biogen has a leading portfolio of medicines to treat multiple sclerosis, has introduced the first approved treatment for spinal muscular atrophy, and developed the first and only approved treatment to address a defining pathology of Alzheimer’s disease. ...

BySage Therapeutics


August 2022 is Spinal Muscular Atrophy Awareness Month!

August 2022 is Spinal Muscular Atrophy Awareness Month!

Every year, the month of August is nationally recognized as Spinal Muscular Atrophy (SMA) Awareness Month. This month-long awareness campaign serves as an important time to demonstrate support and help promote awareness for this rare disease affecting lives across the world. ...

ByControl Bionics, Inc.


New Startup Makes Developing Gene Therapies Faster and Easier

New Startup Makes Developing Gene Therapies Faster and Easier

Today, cell and gene therapies treat and could even cure terminal diseases like leukemia and spinal muscular atrophy, but unlocking their full potential is still a challenge for therapy developers. ...

ByCell Manufacturing Technologies (CMaT)


Haymarket Medical Network Launches Rare Disease Advisor

Haymarket Medical Network Launches Rare Disease Advisor

” The first 13 rare diseases to be focused on, organized as “Junctions,” include: Spinal Muscular Atrophy (SMA), Idiopathic Pulmonary Fibrosis (IPF), Medullary Thyroid Carcinoma (MTC), Pulmonary Arterial Hypertension (PAH), Gastrointestinal Stromal Tumor (GIST), Duchenne Muscular Dystrophy (DMD), Alagille Syndrome ...

ByHaymarket Media Group


BillionToOne to present series of single-gene NIPT posters at 2020 ACMG Annual Clinical Genetics Meeting

BillionToOne to present series of single-gene NIPT posters at 2020 ACMG Annual Clinical Genetics Meeting

UNITY improves clinical specificity for cystic fibrosis carrier screening UNITY is the only prenatal screen that tests cell-free fetal DNA for cystic fibrosis, spinal muscular atrophy (SMA), sickle cell disease, and alpha and beta thalassemia using just one tube of blood from the mother. ...

ByBillionToOne Inc.


BillionToOne to present single-gene NIPT poster at 40th SMFM conference

BillionToOne to present single-gene NIPT poster at 40th SMFM conference

A non-invasive prenatal test for Alpha Thalassemia Hb Barts and Hb Constant Spring UNITY is the only prenatal screen that tests cell-free fetal DNA for cystic fibrosis, spinal muscular atrophy (SMA), sickle cell disease, and alpha and beta thalassemia using just one tube of blood from the mother. ...

ByBillionToOne Inc.


Vybion Huntington`s Disease Drug Patent receives Track I Status

Vybion Huntington`s Disease Drug Patent receives Track I Status

The INT41 patent application covers several neurodegenerative diseases in addition to Huntington's Disease including Spinal Cerebellar Ataxia, Spinal Muscular Atrophy, and Alzheimer's. "Vybion is pleased to receive Track I status on INT41 and anticipates rapid review and allowance" said Lee Henderson, Vybion CEO. ...

ByVybion

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