Bristol-Myers Squibb receives U.S. FDA breakthrough therapy designation for all-oral daclatasvir dual investigational regimen for chronic hepatitis C
24 February 2014 | By Bristol-Myers Squibb Company
Bristol-Myers Squibb Company announced that the U.S. Food and Drug Administration has granted its investigational DCV Dual Regimen Breakthrough Therapy Designation for use as a combination therapy in the treatment of genotype 1b chronic hepatitis C infection...