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FDA approves world-first gene editing treatment: Sickle cell therapy gives hope to 100,000 Americans with incurable disease - but it ll cost millions of dollars per DOSE

In a ground-breaking decision, the Food and Drug Administration approved the first gene therapies to treat people with sickle cell disease

United statesSan antonioUnited kingdomRegina hartfieldSamarth kulkarniJulie kanterLos angelesReshma kewalramaniVertex pharmaceuticalsSickle cell disease association of america incDrug administrationBoston based vertex pharmaceuticalsCrispr therapeuticsSwitzerland based crispr therapeuticsNobel prizeBluebird bio

IBB: Failing Growth Narratives & Overvaluation In Biotech (NASDAQ:IBB)

Biotech stocks enjoyed strong hype and trajectories in the recent past, especially during the pandemic years. Find out why the sector isn't very attractive now.

United statesUnited kingdomCayman islandsSandeepg raoExchange traded products etpsAtai life sciencesExchange traded fundsShares biotechnologyInvesco dynamic biotechVaneck biotechAssets under managementArk investHistorical ratio analysisNorth americanSwitzerland based crispr therapeuticsStar rating

Beam Therapeutics Cofounder And Crispr Scientist Publishes Research On New Sickle Cell Treatment In Mice

Each year more than 300,000 babies around the world, most of them Black, are diagnosed with the painful and life-threatening sickle cell disease.

United statesDavid liuBroad instituteHarvard universityJude children research hospitalJude childrenResearch hospitalSwitzerland based crispr therapeuticsMassachusetts based editas medicineMassachusetts based beam therapeuticsBeam therapeuticsGene editingSickle cell diseaseSickle cellஒன்றுபட்டது மாநிலங்களில்டேவிட் லியூ

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