Dec 8 (Reuters) - The U.S. Food and Drug Administration
on Friday approved two gene therapies for sickle cell disease
from Vertex Pharmaceuticals VRTX.O and CRISPR Therapeutics
CRSP.BN , as well as from bluebird bio BLUE.O .
Sickle cell disease is a painful, inherited blood disorder
that can be debilitating and lead to premature death. It affects
an estimated 100,000 people in the United States, most of whom
are Black.
(Reporting by Sriparna Roy, Leroy Leo and Bhanvi Satija in
Bengaluru;
Editing by Caroline Humer and Bill Berkrot)
((Sriparna.Roy@thomsonreuters.com;))