Bristol-Myers Squibb & Gilead Sciences v Teva / efavirenz (NOC) 2015 FCA 3 Near JA:
Dawson, Stratas JJA aff’g 2014 FC 30 Barnes J
2,279,198 / efavirenz / ATRIPLA
In this NOC proceeding, the FCA has affirmed Barnes J’s decision that the patentee failed to
established that Teva’s product would infringe the ‘198 patent for a particular crystalline form of
efavirenz. The decision at first instance (blogged here) turned entirely on the facts, and the FCA
affirmed on the basis that the appellant patentee had not established and palpable and overriding
error.
The only point of general legal interest is that the FCA held that when non-infringement is
alleged in an NOC proceeding, there is no evidentiary burden on a generic to adduce evidence in
order to put that allegation “in play.” It is enough to make the allegation in the NOA, and the
burden is then on the patentee to prove infringement on the balance of probabilities [11], [8].
This is in contrast to an allegation of invalidity, in which the generic must adduce some evidence
to put the allegation of invalidity into play before the burden shifts to the patentee to disprove
invalidity. The reason for the difference is the presumption of validity under s 43(2) of the Act
[10].
No comments:
Post a Comment