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Nippon Shinyaku : The European Commission Grants Orphan Drug Designation to NS-089/NCNP-02 for the Treatment of Duchenne Muscular Dystrophy -December 21, 2023 at 01:06 am EST

NEWS RELEASE December 21, 2023 The European Commission Grants Orphan Drug Designation to NS-089/NCNP-02 for the.

Toru nakaiKazuyuki nakagomeEuropean commission grants orphan drug designationEuropean unionEuropean commissionNippon shinyaku co ltdNational centerDrug administrationDuchenne muscular dystrophyNippon shinyakuOrphan drug designationRare pediatric disease designationBreakthrough therapy designationKodaira city

NS-089/NCNP-02 Preclinical Data Published in Molecular Therapy Nucleic Acids

/PRNewswire/ NS Pharma, Inc. announced today the publication of preclinical data on NS-089/NCNP-02 (brogidirsen), an investigational candidate for patients.

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FDA Grants Orphan Drug Designation to NS-089/NCNP-02 for the Treatment of Duchenne Muscular Dystrophy

FDA Grants Orphan Drug Designation to NS-089/NCNP-02 for the Treatment of Duchenne Muscular Dystrophy
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United statesKazuyuki nakagomeToru nakaiTsugio tanakaNational centerPrnewswire ns pharma incNs pharma incUs food drug administrationNippon shinyaku co ltdNippon shinyakuDrug administrationOrphan drug designationOrphan drug designationsRare pediatric disease designationBreakthrough therapy designationKodaira city

/C O R R E C T I O N -- NS Pharma/

/C O R R E C T I O N -- NS Pharma/
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FDA Grants Rare Pediatric Disease Designation to NS-089/NCNP-02 for the Treatment of Duchenne Muscular Dystrophy

/PRNewswire/ NS Pharma, Inc. announced today the U.S. Food & Drug Administration (FDA) has granted Rare Pediatric Disease Designation to NS-089/NCNP-02.

United statesKazuyuki nakagomeToru nakaiTsugio tanakaUs food drug administrationNs pharma incNippon shinyaku co ltdNational centerNippon shinyakuDrug administrationRare pediatric disease designationPediatric disease designationNeurological medicineKodaira cityDuchenne muscularRns pharma