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United States Food & Drug Administration (FDA) Grants Mesoblast Orphan-Drug Designation for Revascor® (Rexlemestrocel-L) in Children With Congenital Heart Disease

United States Food & Drug Administration (FDA) Grants Mesoblast Orphan-Drug Designation for Revascor® (Rexlemestrocel-L) in Children With Congenital Heart Disease
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United statesSteve dabkowskiSilviu itescuPaul hughesMesoblast limited nasdaqMesoblast the companyAustralian securities exchangeDrug administrationDrug designation programCorporate communications investorsJournal of the american college cardiologyUnited states foodOrphan drug designationRare pediatric disease designationChief executive silviu itescuCardiovascular surgery open

United States Food & Drug Administration (FDA) Grants

NEW YORK, Feb. 14, 2024 (GLOBE NEWSWIRE) Mesoblast Limited (Nasdaq:MESO; ASX:MSB), global leader in allogeneic cellular medicines for inflammatory.

United statesSteve dabkowskiSilviu itescuPaul hughesDrug administrationCorporate communications investorsAustralian securities exchangeMesoblast the companyDrug designation programMesoblast limited nasdaqJournal of the american college cardiologyUnited states foodOrphan drug designationRare pediatric disease designationChief executive silviu itescuCardiovascular surgery open

NetworkNewsWire: Pathways to Progress: How Orphan Drug Designation Sparks Biotech Transformation

NetworkNewsWire: Pathways to Progress: How Orphan Drug Designation Sparks Biotech Transformation
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New yorkUnited statesBaden wübergSophia randolphGenentech tecentriqRodney varnerExchange commissionGenentech incJazz pharmaceuticalsGenprex incDrug administrationEuropean commissionUs food drug administrationOncology holdings incNational library of medicineAchilles therapeutics

Assessing the Impact of the Orphan Drug Act 40 Years Later

The act was passed in 1983 and has contributed to increased research and development on treatments for rare diseases.

United statesDrug designation programOrphanet journalOrphan drug actOrphan drug designation programOrphan drug designation programOrphan drugOrphan drug approvalsRare disease drug development

Omega Therapeutics Reports Third Quarter 2022 Financial Results and Recent Corporate Highlights

/PRNewswire/ Omega Therapeutics, Inc. (Nasdaq: OMGA) ("Omega"), a clinical-stage biotechnology company pioneering the first systematic approach to use mRNA.

United statesUnited kingdomJason bracoEva stroynowskiMahesh karandeOmega epigenomicDevelopment pipelineDrug designation programAmerican society of gene cell therapyDrug administrationPrnewswire omega therapeutics incDevelopment activities for several oecsOmega therapeutics incLifesci communicationsFirst patient dosedOrphan drug designation