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Editas Medicine to Present Clinical Data from the RUBY and EdiTHAL Trials of Reni-cel at the European Hematology Association 2024 Congress in June

Editas Medicine to Present Clinical Data from the RUBY and EdiTHAL Trials of Reni-cel at the European Hematology Association 2024 Congress in June
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United statesUnited kingdomHaydar frangoulHall velasquezCristi barnettRabi hannaBaisong meiEuropean hematology associationHarvard university casExchange commissionEditas medicine incEuropean hematology association congressDepartment of pediatric hematology oncologyBroad instituteBroad institute casPresent clinical data

Exa-Cel Eliminates Vaso-Occlusive Crises in Most Sickle Cell Patients

Ninety-seven percent of patients were free from vaso-occlusive crises for at least 12 consecutive months.

United statesHaydar frangoulVertex pharmaceuticalsSarah cannon research instituteHealthday newsNew england journalTristar centennial

Researchers publish final results of key clinical trial for gene therapy for sickle cell disease

Researchers publish final results of key clinical trial for gene therapy for sickle cell disease
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United statesStephana gruppExagamglogene autotemcelHaydar frangoulGene therapy laboratoryStephenp kelly centerNational institutes of healthNational institutesNew england journalSection chiefCellular therapyTransplant sectionInaugural directorMedical directorSevere sickle cell disease

Exa-cel a first step in gene therapy for sickle cell disease, beta-thalassemia

Exa-cel a first step in gene therapy for sickle cell disease, beta-thalassemia
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San franciscoUnited statesByjosh friedmanHaydar frangoulP josephm mccuneHanspeter kiemMindy valcarcelFred hutch cancer centerSarah cannon research instituteVertex pharmaceuticalsUniversity of californiaNew england journalTristar centennial children

Gene-Editing Therapy Helps Nashville Sickle Cell Patients | City Limits

In early December, CRISPR-Cas9 gene editing therapy was approved by the Food and Drug Administration for the treatment of sickle cell in patients ages 12 and up. It’s the first FDA approval for the gene-editing therapy, whose creators won the Nobel Prize in chemistry in 2020.

United statesAlyssa weddleHaydar frangoulDrug administrationCellular therapy program at tristar centennialTristar centennialNobel prizeSarah cannon pediatric transplantCellular therapy programAfrican americanSickle cell diseaseSickle cellHealth careGene editingTristar centennialHaydar frangoul