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Crispr Gene Editing: FDA Approves First Genetic Therapy That Might Cure Sickle Cell

The Food and Drug Administration approved a new gene editing therapy for sickle cell disease, its first green light for a Crispr treatment.

United kingdomReshma kewalramaniDrug administration onVertex pharmaceuticalsDrug administrationBoston based vertex pharmaceuticalsCrispr therapeuticsPresident reshma kewalramaniFirst crispr gene editing therapyFood and drug administrationSickle cellGene editingExa cel

CRISPR: The gene-editing technology, explained

The Food and Drug Administration on Friday approved the first drug that uses this technology to treat an illness, sickle cell disease.

United statesDana farber cancer instituteJennifera doudnaGeorge churchEmmanuelle charpentierJennifer doudnaFeng zhangStuart orkinMax planck institute for infection biologyVertex pharmaceuticalsF gilbert associatedDrug administration onAlexander heinl associatedUniversity of californiaCenters for diseaseHoward hughes medical institute investigator

The first CRISPR therapy approved in the U S will treat sickle cell disease

In the world’s first CRISPR-based treatment, genetic tweaks to red blood cells aim to help people with the often debilitating disease.

New yorkUnited statesUnited kingdomDavid altshulerWilliam hobbsKerry morroneJimi olaghereAlbert einstein college of medicineDrug administrationSickle cell programVertex pharmaceuticalsNobel prizeBoston based vertex pharmaceuticalsAlbert einstein collegeVictoria gray

FDA Approves Two Gene Therapies For Sickle Cell Patients, Including One That Uses CRISPR Tech - Giving Hope To 100,000 Americans With Incurable Disease » WhatsNew2Day

In a groundbreaking decision, the Food and Drug Administration approved the first gene-editing therapy to treat patients with sickle cell anemia, a crippling

United statesUnited kingdomDrug administrationVertex pharmaceuticalsBoston based vertex pharmaceuticalsCrispr therapeuticsNobel prize

FDA considers first CRISPR gene editing treatment that may cure sickle cell

A cutting-edge therapy that is currently under review offers the sickle cell community something many haven’t ever had before: hope.

United statesDaniel bauerStephanie krogmeierScot wolfeFyodor urnovLakiea baileyVertex pharmaceuticalsDrug administrationBlood disorders centerVertex pharmaceuticals incorporatedUmass chan medical schoolUniversity of californiaSickle cell consortiumDepartment of molecularBoston based vertex pharmaceuticalsCell biology

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