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On the basis of these new preclinical results with LentiGlobin vector BB305 and the sustained positive outcome for a patient with the parental LentiGlobin vector HPV569 [170], both the ANSM (French) and the RAC/FDA (Recombinant DNA Advisory Committee/Federal Drug Administration, US) granted us approval, in 2013 and 2014, for three new clinical trials using LentiGlobin vector BB305 sponsored by the biotechnology company bluebird bio: (1) Trial NCT02151526 (HGB-205) in France, for both beta-thalassemia and sickle cell disease, (2) Trial NCT01745120 (HGB-204) at multiple centers in the US, Australia and Thailand, for beta-thalassemia, and (3) Trial NCT02140554 (HGB-206), at multiple centers in the US, for sickle cell disease

All of this is still being studied in depth, including dosing regimens, dosing frequencies, and the solvents to be used

After rats had recovered from anaesthesia they were allowed to consume commercial laboratory food and drink tap water ad libitum

Follow-Up Testing Schedule Recheck your panel at 6 weeks after starting, then again at 12 weeks, and every 12 weeks thereafter