"The most significant value driver, however, is anti- VEGF drug Eylea following positive FDA panel recommendation for approval and a potential $3.5B opportunity in eye disease. Expert feedback suggests that superior efficacy and less frequent dosing should position Eylea favorably to $4B brand Lucentis, and we expect HARBOR and CATT two- year data to confirm a differentiated profile."
The BMO analyst is merely saying that investors’ expectations for BG-12 got too high based on the data from one clinical trial (DEFINE) in which the comparator was placebo. Unless the outcome of the CONFIRM study is truly awful for Copaxone, I don’t expect the trial to have much commercial impact on Copaxone for the reason mentioned in #msg-62332894.
A reliable test to distinguish high-risk DCIS from low-risk DCIS would have a lot of value, IMO. However, I haven’t studied this test closely enough to have a strong opinion on whether it will succeed in this setting. Comments?