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FDA Staff Raises Concerns Over Lack of Safety Data for Sickle-Cell Treatment

(Bloomberg) -- The Food and Drug Administration’s staff raised concerns about safety data on a potential gene-editing treatment for sickle cell disease, ahead of a closely watched meeting where scientific experts will weigh the first therapy using Crispr technology. Most Read from BloombergHouse Speaker Mike Johnson’s First Big Bill Cuts Biden’s Climate Change FundingUS Military Attacks Two Syrian Facilities It Says Linked to IranIsrael Latest: US Strikes Two Iran-Linked Fac...
United States Bloomberg Businessweek Fiona Rutherford Vertex Pharmaceuticals Inc American Society Of Hematology Drug Administration
Source: yahoo.com

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Pamplin Media Group - Bioethicist calls for moratorium on 'designer babies'

Bioethicist calls for moratorium on designer babies Genetically engineered humans are now a reality, expert tells City Club of Portland. A bioethicist-in-residence at the University of Oregon on Thursday, Feb. 18, said the time is now to institute a temporary halt on research into editing the human genome for future generations Franรงoise Baylis, the 2020-21 Wayne Morse Chair at the schools Wayne Morse Center for Law and Politics said in a virtual discussion hosted by the City Club of ...
University Of Oregon United States Portland State University Francoise Baylis Emmanuelle Charpentier Wayne Morse

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