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FDA grants Priority Review for Lucentis in diabetic retinopathy

9 October 2014 | By Roche

Roche announced that the U.S. Food and Drug Administration has accepted to file the company's supplemental Biologics License Application and granted Priority Review of Lucentis (ranibizumab injection) for the treatment of diabetic retinopathy, an eye disease that impacts nearly 7.7 million Americans...

Bristol-Myers Squibb statement about Asunaprevir in the U.S.

9 October 2014 | By Bristol-Myers Squibb Company

Given the rapidly evolving hepatitis C treatment landscape in the U.S., Bristol-Myers Squibb has decided that it will not pursue U.S. Food and Drug Administration approval of the dual regimen of daclatasvir and asunaprevir for the treatment of HCV genotype 1b patients in the United States...

Bristol-Myers Squibb statement on Sustiva (efavirenz) in the U.S.

8 October 2014 | By Bristol-Myers Squibb Company

Bristol-Myers Squibb Company has successfully resolved all outstanding U.S. patent litigation relating to efavirenz, an active ingredient contained in our Sustiva (efavirenz) and Atripla (efavirenz/emtricitabine/tenofovir disoproxil fumarate) products...