Novartis Pharmaceuticals Australia Pty Ltd v Bayer Australia Limited
[2013] FCA 929
At a glance
Source factsCourt
Federal Court of Australia
Decision date
2013-09-13
Before
Robertson J
Source
Original judgment source is linked above.
Judgment (3 paragraphs)
The interlocutory application 1 By interlocutory application filed on 22 August 2013, the applicant seeks leave to amend its further amended statement of claim in accordance with the amendments detailed in annexure RDM - 10 of the affidavit of Ross David McInnes affirmed on 22 August 2013. 2 That affidavit was read by the applicant on the hearing of the interlocutory application yesterday. No evidence was relied on by the respondent. 3 The amendments proposed are in substance as follows: 28G. During the course of 2012 and/or 2013 Bayer company representatives engaged in communications with ophthalmologists and/or optometrists (known as "detailing") during which the ophthalmologists and/or optometrists were shown in detail aids which included word [sic] in terms substantially similar to those in paragraph 28A above ("Detailing Conduct"). 4 The words in paragraph 28A referred to were as follows: EYLEA® FOR YOU AND YOUR PATIENTS WITH FEWER INJECTIONS WHEN USED ACCORDING TO THE APPROVED DOSAGE COMPARED TO MONTHLY LUCENTIS®1, 2 … References: 1. EYLEA Product Information. 2. LUCENTIS Product Information. 5 It was also sought to amend to add paragraph 32B in relation to the four representations already pleaded that those representations "were also conveyed by officers and/or employees of the [sic] Bayer in the course of the Detailing Conduct." 6 The representations were set out in paragraph 29 of the pleading and were: 29.1 that in clinical use, in accordance with the approved dosage, Lucentis is administered monthly for all patients ("First Representation"); 29.2 that, for each and every patient, Lucentis will only be a clinically effective treatment if administered monthly ("Second Representation"); 29.3 that the Lucentis Product Information specified, without qualification, that it was to be administered monthly ("Third Representation"); 29.4 that in accordance with approved dosages, all Eylea patients receive fewer injections than all Lucentis patients ("Fourth Representation").