One area that I find mildly surprising with Momenta is that they are not doing more to pursue the other options that they are finding in their quest for biogenerics. If you read their patent estate it is clear that there are lots of opportunities and I am not suggesting that they should pursue them all - but, for instance, creating a small arm of the company to filter a few of these and pursue them clinically would seem worthwhile.
Does your “other options” refer to: a) more ANDA’s for complex drugs regulated as small molecules such as Lovenox and Copaxone; or b) protein drugs regulated by the new 351(k) pathway? Please clarify.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”