Reuters reported last week that the move was imminent. It marks the
latest sign of a renaissance in gene therapy after some disastrous
clinical trial results in the late 1990s and early 2000s.
GSK's product, developed with Italian scientists, is designed to
treat a tiny number of children with ADA Severe Combined Immune
Deficiency (ADA-SCID) for whom no suitable bone marrow donor can be
found.
(Reporting by Ben Hirschler; editing by Jason Neely)
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