Dockets:
T-504-12
T-505-12
Citation: 2014 FC 525
Ottawa, Ontario, May 30, 2014
PRESENT: The Honourable Madam Justice Gleason
Docket:
T-504-12
|
BETWEEN:
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ALCON CANADA INC., ALCON RESEARCH LTD., ALCON PHARMACEUTICALS,
LTD. AND KYOWA HAKKO KIRIN CO., LTD.
|
Applicants
|
and
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COBALT PHARMACEUTICALS COMPANY AND THE MINISTER OF HEALTH
|
Respondents
|
|
Docket:
T-505-12
|
AND
BETWEEN:
|
ALCON CANADA INC., ALCON RESEARCH, LTD., AND KYOWA HAKKO KIRIN
CO., LTD.
|
Applicants
|
and
|
COBALT PHARMACEUTICALS COMPANY AND THE MINISTER OF HEALTH
|
Respondents
|
ORDER AND REASONS
(Regarding
costs)
[1]
The applicants [called, collectively, “Alcon” in
these Reasons] commenced two prohibition applications, seeking to restrain the
Minister of Health [the Minister] from issuing Notices of Compliance [NOCs]
under the Patented Medicines (Notice of Compliance) Regulations, SOR/93-133 [the NOC
Regulations] to the respondent, Cobalt Pharmaceuticals Company [Cobalt],
for eye drops containing 0.1% and 0.2% concentrations of olopatadine. The
application in respect of the 0.1% solution was made in Court File T-505-12 and
that in respect of the 0.2% solution in Court File T-504-12.
[2]
Both applications were scheduled to be argued
before me over the course of five days between December 9 and 13, 2013. On
December 4, 2013, Alcon discontinued its application in Court File T-505-12 and
advised that it was not relying on Canadian Patent No. 2,195,094 [the 094
Patent] in respect of its application in Court File T-504-12. In my Judgment in
Alcon v Cobalt, 2014 FC 149, issued on February 14, 2014, I dismissed
Alcon’s application to prohibit the Minister from issuing an NOC to Cobalt for
its 0.2% olopatadine ophthalmic solution product and directed Alcon and Cobalt
to provide submissions on costs in respect of both applications.
[3]
These Reasons deal with costs in both files.
I.
Court File T-505-12
[4]
The Notice of Application in this matter was
filed on March 8, 2012 and, as noted, the application was discontinued just five
days before it was scheduled to be argued.
[5]
Cobalt seeks solicitor-client costs in this file
in the amount of $430,000.00, payable forthwith, which it alleges is equal to the
actual costs it incurred in this matter from April 12, 2012 to December 4, 2013
as well as its estimated fees in relation to the costs submissions. In the
alternative, Cobalt seeks a lump sum award, beyond the upper end of Column V of
Tariff B to the Federal Courts Rules, SOR/98-106 [the Rules], in the
amount of $200,000.00, likewise payable forthwith. It argues that Alcon’s
conduct merits censure and the imposition of either solicitor-client costs or
an elevated costs award.
[6]
Cobalt’s claims in this regard centre on what
transpired in an earlier prohibition application in respect of the 094 Patent
that Alcon commenced against Apotex Inc. [Apotex] in respect of that company’s
0.1% olopatadine ophthalmic solution in Court File T-564-10. That application
was heard by my colleague, Justice Barnes, who reserved his decision on the
merits. Following the hearing, Alcon and Apotex jointly requested that the
decision not be released as they were attempting to settle the application. On
consent, counsel for Alcon wrote to the Court on March 30, 2012 and requested
that Justice Barnes not release his decision until April 12, 2012, the day
before the statutory stay was set to expire. However, counsel’s March 30, 2012
letter was not brought to Justice Barnes’ attention, and he issued his decision
in Court File T‑564‑10 on April 11, 2012 [Justice Barnes’ Decision].
In it, he dismissed Alcon’s prohibition application, finding that the 094
Patent failed on the ground of obviousness.
[7]
Almost immediately thereafter, counsel for Alcon
wrote to counsel for Apotex, indicating he had received instructions to request
the Court that it:
… retract the decision if possible, because i)
the parties had asked that it not be released until April 12, pending
settlement; and ii) the parties have now reached agreement on all material
points and were at the point of today asking the Court for an extension of the
statutory stay period, by one month, pending putting together a formal
agreement.
[8]
It appears from the decision of Justice Mesbur
in Alcon Canada Inc v Apotex Inc, 2013 ONSC 4897, about which more is said
below, that counsel for Apotex received instructions to agree to this proposal,
called the Registry of this Court on April 11th and conveyed the
message he and counsel for Alcon had agreed to. However, the Registry appears
to have advised Justice Barnes that Alcon and Apotex had requested withdrawal
of his Judgment as they had settled the application. Therefore, on April 12,
2013 Justice Barnes issued the following Direction:
Upon being advised by the parties that a full
settlement of this litigation has been negotiated coincidental with the
issuance of the Court’s Judgment and with their consent the Court’s Judgment is
hereby withdrawn.
[9]
The next day, Alcon filed a Notice of
Discontinuance with the Court in the prohibition application involving Apotex’s
0.1% olopatadine solution.
[10]
Thereafter, Alcon and Apotex continued their discussions
but were unable to agree to final settlement documentation. In October of 2012,
Alcon made an application to the Ontario Superior Court of Justice to enforce
the settlement it claimed it had reached with Apotex.
[11]
On July 22, 2013, Justice Mesbur released her
decision in Alcon’s application to enforce the settlement and decided that no
settlement had been reached because both parties had negotiated on the basis
that any agreement they reached was tentative and subject to the approval of
their respective principals. As this approval was not given by Apotex (after it
learned of the outcome reached by Justice Barnes), Justice Mesbur held that the
prohibition application in respect of Apotex’s 0.1% olopatadine product had not
been settled. Alcon did not appeal Justice Mesbur’s decision.
[12]
In August of 2013, Apotex wrote to this Court
seeking to rely on Justice Barnes’ Decision in connection with another
proceeding between Apotex and Alcon involving olopatadine where Alcon was
relying in part on the 094 Patent. In the context of the subsequent back and
forth between Apotex and Alcon, Apotex argued that the withdrawn decision should
be reinstated. Alcon disagreed. Ultimately, Apotex decided not to pursue the
reinstatement of Justice Barnes’ Decision.
[13]
In October of 2013, Cobalt wrote to this Court, also
seeking reinstatement of Justice Barnes’ Decision. In his October 22nd
letter to the Court, counsel for Cobalt stated that his client first learned of
the outcome in the withdrawn decision when Justice Mesbur’s decision was
released in July 2013. However, it appears from the materials filed by Cobalt
in connection with its claim for costs in this matter that counsel for Cobalt
reviewed the recorded entries in this Court’s file in the Alcon-Apotex
prohibition matter in April 2012. Those entries reveal that a Judgment had been
issued on April 11, 2012 and was withdrawn on consent the following day due to
a settlement having been reached by the parties. The entries, however, did not
reveal the outcome reached in the withdrawn Judgment. Thus, in April 2012
Cobalt was aware only that Justice Barnes’ Decision had been withdrawn, but did
not learn of the outcome reached by Justice Barnes until July 2013.
[14]
On December 3, 2013, Justice Barnes held a
hearing to deal with Cobalt’s request to reinstate his Decision; Alcon argued
against the Decision’s being reinstated.
[15]
Justice Barnes granted Cobalt’s motion from the
bench, issued his Decision nunc pro tunc as of April 11, 2012 and
awarded Cobalt costs on the reinstatement motion in the amount of $10,000.00,
payable by Alcon. In so awarding Justice Barnes was critical of the conduct of
Alcon (and Apotex), stating at page 5 of his Order that he:
disagree[d] with Alcon’s argument that by
filing a Notice of Discontinuance, the Court is deprived of the jurisdiction to
grant relief. It is not open to any party to obtain an order on the strength of
the miscommunication or misunderstanding by the Court and then to preserve the
effect of the order by unilaterally discontinuing the proceeding. That is
particularly obvious where the interests of third parties may be engaged. To
permit such an outcome would be to abuse the Court process …
[16]
Cobalt argues that Alcon’s conduct in filing a
Notice of Discontinuance and subsequently failing to advise Justice Barnes that
the matter had not settled, when it became apparent that Apotex was resisting
consummating the settlement, merits an award of solicitor-client or elevated costs
because Alcon’s conduct resulted in Cobalt’s being required to incur substantial
costs, which were wholly unnecessary. Cobalt asserts in this regard that Justice
Barnes’ Decision necessarily required that Alcon discontinue the prohibition
application against Cobalt in Court File T-505-12 as the same issues as were
decided by Justice Barnes arose in the application against Cobalt and it would
have been an abuse of process for Alcon to re-litigate these issues (relying in
this regard on Sanofi-Aventis Canada Inc v Novopharm Limited, 2007 FCA
163 [Sanofi-Aventis]).
[17]
Alcon, on the other hand, asserts that costs in
respect of this matter should only be awarded based on the mid-point of Column III
of Tariff B, making five arguments in support of its position. It first argues
that Cobalt knew about the withdrawn decision in April 2012 but neglected to
take any action to have it reinstated until October 2013, thereby prolonging
the pursuit of the application in respect of the NOC for the 0.1% olopatadine
product. Second, Alcon asserts that it acted in good faith in seeking to uphold
the settlement agreement and that, at least until the release of Justice
Mesbur’s decision, there is no basis for an elevated costs award. Third, it
argues that even after Justice Mesbur’s determination, its conduct was
reasonable as there is no precedent for dealing with a situation of this nature
and it was therefore not clear that it needed to discontinue the application
against Cobalt or to advise the Court as to what had transpired in the Ontario
application. Fourth, Alcon argues that the case law relied on by Cobalt in
support of an elevated cost award is distinguishable and involved much more
objectionable conduct, like the deliberate repeated disregard of a plaintiff’s
trade-mark rights and past court judgments (in Louis Vuitton v Lin
Pi-Chu Yang, 2007 FC 1179 [Louis Vuitton]) or deliberate and
unnecessary attempts to re-litigate the same issues against the same party (in Apotex
v Merck, 2005 FCA 24 [Apotex v Merck] and Benisti Import-Export
Inc v Modes Txt Cardon Inc, 2002 FCT 810 [Benisti]). Finally, Alcon
asserts that it would not have been an abuse of process for it to re-litigate
the validity of the 094 Patent in the application to prohibit the Minister from
issuing an NOC to Cobalt for the 0.1% olopatadine solution, intimating that
there was no allegation at issue in the Apotex application that was also
present in the application it brought in respect of Cobalt.
[18]
I disagree with the final assertion and find
that it would have been an abuse of process for Alcon to have litigated its
application against Cobalt in respect of the 094 Patent after Justice Barnes’
Decision was reinstated because the same issue was raised by Cobalt. As
noted, Justice Barnes dismissed the prohibition application against Apotex because
he found that the 094 Patent failed on the ground of obviousness. Very similar allegations
regarding obviousness were made by Cobalt in Court File T-505-12. Thus, the
decision in Sanofi-Aventis is dispositive; it provides that it is an
abuse of process, within the meaning of paragraph 6(5)(b) of the NOC
Regulations, for an innovator company to re-litigate the same allegations that
were ruled upon in a previous prohibition application involving a different
generic company, even if the allegations are differently worded in the Notices
of Allegation in the two files or if the innovator company seeks to call
different evidence in the second file.
[19]
The case of Nycomed Canada Inc v Canada (Minister of Health), 2008 FC 541 [Nycomed], relied on by Alcon to
substantiate a different conclusion, does not assist it as that case involved a
situation completely different from the present. In Nycomed, what was at
issue was whether a generic company had infringed an innovator’s use-based
patent. In a previous case, the Court had struck a similar claim of
infringement brought against another generic company. In Nycomed,
Prothonotary Tabib held that the situation was distinguishable from that in Sanofi-Aventis
(and that there was no re-litigation of an issue so as to constitute an abuse
of process within the meaning of paragraph 6(5)(b) of the NOC Regulations)
because what was at issue in the two cases was different – namely whether the
conduct of two different generic companies constituted infringement. In Sanofi-Aventis,
on the other hand, what was at issue in the two cases was the validity of the
patent for failure to soundly predict utility. That issue was the same in both
cases and arose directly from the patent, itself.
[20]
For the reasons already noted, the present case
and the previous ruling made by Justice Barnes on the obviousness of the 094
Patent involve the same allegation, and, therefore, the holding in Sanofi-Aventis
applies such that it would have been an abuse of process for Alcon to re-litigate
the validity of the 094 Patent against Cobalt. Indeed, as Cobalt aptly notes,
this is eloquently demonstrated by the fact that Alcon discontinued its
application against Cobalt the day after Justice Barnes’ Decision was
reinstated.
[21]
As for the other grounds advanced by Alcon,
contrary to what it claims, I do not believe that it behaved reasonably
throughout. Rather, I concur with Justice Barnes that, especially once Justice
Mesbur determined that Alcon had no agreement with Apotex to settle the prohibition
application involving Apotex, it was incumbent on Alcon (and, indeed, Apotex)
to so advise this Court to afford Justice Barnes the opportunity to re-instate
his Decision. The failure to do so did affect third parties, including Cobalt.
Cobalt was required to continue in its preparation of its defence in respect of
the prohibition application in Court File T-505-12 (and to advance the
arguments related to the 094 Patent in Court File T-504-12). In addition,
Cobalt’s generic version of the 0.1% olopatadine eye drop was kept off the
market for approximately six additional months, thereby possibly causing Cobalt
losses and possibly depriving members of the Canadian public of its product
over this period.
[22]
I also disagree with Alcon that Cobalt was dilatory
in raising the status of the withdrawn Decision. It did not know of the outcome
reached until July 2013, when Justice Mesbur issued her decision in the Ontario proceeding. Without knowing this, there was no basis for Cobalt to have sought to
have Justice Barnes’ Decision reinstated since a decision granting the
application would not necessarily have been binding against Cobalt (see e.g. Apotex
Inc v Janssen-Ortho Inc et al, 2009 FCA 212). Moreover, as concerns the
three months between when Cobalt learned of Justice Mesbur’s decision and the
date it filed its application to have Justice Barnes’ Decision reinstated, I do
not view any delay on Cobalt’s part as unreasonable for two reasons. First, and
most importantly, as Justice Barnes determined, the primary onus to correct the
record before this Court lay with Alcon and Apotex, not Cobalt. Secondly,
Apotex, itself, had raised the issue of the status of the withdrawn Decision with
the Court as early as August 2013, so any delay by Cobalt to also raise the
issue is not material.
[23]
In the circumstances, I find that an award of
solicitor-client costs for a portion of the time that Cobalt seeks them is
warranted. Solicitor-client costs are very much the exception and should only
be awarded when one party engages in conduct that deserves sanction, which has
often been described as conduct that is “reprehensible, scandalous or
outrageous” (see e.g. Young v Young, [1993] 4 S.C.R. 3 at para 66; Louis
Vuitton at para 55; Chrétien v Gomery, 2011 FCA 53 at para 3). Here,
I find that Alcon’s conduct in seeking to avoid the impact of Justice Barnes’ Decision,
after it became clear there was no settlement, and in continuing its
application against Cobalt until the eleventh hour in circumstances where it
was clear that the withdrawn Decision would render its conduct an abuse of
process, is so serious that it warrants imposition of costs on the solicitor-client
scale. Its conduct in this regard is analogous to that of the unsuccessful
parties in Apotex v Merck and Benisti, where, rather than
appealing issues, the unsuccessful parties sought to re-litigate them. Just as
an award of solicitor-client costs was appropriate in those cases, it is
appropriate here, because just like the unsuccessful parties in Apotex v
Merck and Benisti, Alcon caused Cobalt to incur expenses that were
wholly unnecessary.
[24]
That said, I am not persuaded that an award of
solicitor-client costs for the entire period Cobalt seeks them is warranted. I
believe that there is merit in Alcon’s position that its conduct prior to July
2013 was reasonable as it sought to enforce the settlement it believed it had
reached, and, indeed, it was Apotex – and not Alcon – which backed away from
the agreement in principle the two had reached once it learned that Justice
Barnes had dismissed the prohibition application in the withdrawn Decision. It
was not until Justice Mesbur decided that there was no settlement that Alcon’s
conduct became so objectionable that an award on a solicitor-client basis is
warranted.
[25]
Thus, Cobalt is entitled to solicitor-client
costs in this matter only from July 23, 2013 (the day after Justice Mesbur’s
decision) to December 4, 2013 (the day Alcon discontinued Court File T-505-12),
inclusive. The costs so awarded include all actual fess paid or payable by
Cobalt for work done within this period, including the full amount of
disbursements incurred in this period.
[26]
For the period before July 23, 2013 and after December
4, 2013 – and in respect of the preparation of its costs submissions – Cobalt
is entitled only to costs on the scale normally applicable in applications of
this nature. While there is some divergence in the case law in terms of what
that scale is, there are several cases which support its being set at the mid-point
of Column IV of Tariff B to the Rules, and for providing for the attendance of
two counsel at the hearing (see e.g. Novartis Pharmaceuticals Canada Inc v
Cobalt Pharmaceuticals Co, 2013 FC 985 at para 112 [Novartis]; Astrazeneca
Canada Inc v Mylan Pharmaceuticals ULC, 2011 FC 1023 at para 231; Novo
Nordisk Canada Inc v Cobalt Pharmaceuticals Inc, 2010 FC 746 at para 370; Pfizer
Canada Inc v Ratiopharm Inc, 2010 FC 612 at para 178; Lundbeck Canada
Inc v Ratiopharm Inc, 2009 FC 1102 at para 403). I find that setting fees
on this basis for all periods before July 23, 2013 and after December 4, 2013
is reasonable given the scope of the issues at play in this file. I also find
that Cobalt is entitled to its reasonable disbursements, which for these
periods would include (if applicable) business class travel on trans-Atlantic
flights for one counsel to attend cross-examinations, as awarded in previous
cases (see e.g. Novartis at para 112; Bayer Inc v Cobalt
Pharmaceuticals Co, 2013 FC 1061 at para 164).
[27]
I find it is appropriate that all work done by
Cobalt on the 094 Patent should be attributed to Court File T-505-12 (and
correspondingly that the only costs associated with Court File T-504-12 are
those incurred in relation to the 924 Patent). This is because regardless of
whether Cobalt’s work on the 094 Patent applied to one file or the other, it
was nonetheless work that Cobalt only had to do because of Alcon’s attempt to re-litigate
the validity of the 094 Patent. At the same time, Cobalt is not entitled to
double recovery for the same work done in relation to two separate files. Indeed,
Cobalt in their costs submissions for Court File T-504-12 has not included any
claims with respect to the 094 Patent.
[28]
Some of Cobalt’s work clearly related only to
either the 094 Patent or the 924 Patent. Work relating to the testimony of
doctors Lightman, Stephan, Yanni, Lieberman and Irani applied only to the 094
Patent. Work relating to the testimony of Dr. Laskar related only to the 924
Patent.
[29]
In many other instances, however, it appears
that Cobalt’s delineation of work between the two patents is not so clear.
Cobalt’s affiant, John Lucas, deposes at para 7 of his affidavit that he was
advised that with respect to the evidence of Dr. Bodmeier, 10% related to the
094 Patent and 90% to the 924 Patent, with a like breakdown for disbursements. Further,
for a significant portion of Cobalt’s work, Mr. Lucas deposes that the timekeeping
descriptors were “not clear enough to discern the specific patent to which it
related”, and so he apportioned 50% to the 094 Patent and 50% to the 924 Patent
(at para 10 of his affidavit). While it is regrettable that Cobalt did not track
its time on these files with greater precision, the 10/90 split for work
related to Dr. Bodmeier and the 50/50 split for the unclear descriptors appear
to be reasonable.
[30]
It would have been preferable had I been able to
quantify a lump sum costs award to give effect to the foregoing determinations,
but, unfortunately, the materials filed by Cobalt in support of its costs claim
do not allow me to do so. As Alcon correctly notes in its submissions, only
fragmentary information has been provided in respect of the disbursements
claimed as no invoices were produced and there is no substantiation for the
basis of some of the items that are claimed. Nor is there any affidavit
attesting to their reasonableness as is normally required under Tariff B to the
Rules, section 1(4). In addition, there is confusion in the time dockets that
were filed by Cobalt, and claims were made for time that is already the subject
of Justice Barnes’ cost award made in the context of the motion to reinstate
his withdrawn Decision. Cobalt is not entitled to double-recovery for these
amounts. Finally, the materials filed do not allow for the calculation of fees
split between those to be calculated on a solicitor-client recovery basis and
those to be assessed at the mid-point of Column IV to the Rules. Thus, I have
refrained from making a lump sum award in this matter and instead remit its
calculation to the parties. I would hope that with the assistance of these Reasons
they should be able to settle the matter themselves. If not, the final
determination of the amounts payable by Alcon to Cobalt in respect of Court
File T-505-12 may be referred to an assessment officer.
II.
Court File T-504-12
[31]
The issues in respect of costs in this file are
much more straight-forward as Cobalt seeks party-and-party costs, and Alcon
agrees that it is bound to pay the same but differs as to the basis for their
calculation. It also disputes that a lump sum should be awarded, noting that
the time claimed for certain items is excessive and that the substantial amount
claimed for disbursements is not properly substantiated.
[32]
For the same reasons as in Court File T-505-12,
I have decided that costs should be awarded at the mid-point of Colum IV of Tariff B to the Rules, that Cobalt is entitled to compensation for two counsel at
the hearing, and that reasonable disbursements include business class airfare for
trans-Atlantic flights to attend cross-examinations for one counsel. However,
as Cobalt has failed to file evidence to support the reasonableness of its
disbursement claim, I decline to make a lump sum award, as Justice Snider
declined to do for much the same reasons in Sanofi-Aventis Canada Inc v
Novopharm Limited, 2009 FC 1139 at para 6.
[33]
As discussed above, only work in relation to the
924 Patent is to be considered for costs purposes as work done in respect of
Court File T-504-12. Where it is not completely clear whether the work done was
related to the 094 Patent or the 924 Patent, the parties shall attempt to agree
between themselves as to the proper apportionment. As noted, the 90%
apportionment of work relating to Dr. Bodmeier’s testimony to the 924 Patent
and the 50% apportionment for work with unclear descriptors seems to be
reasonable. Once again, I trust that with the guidance of these Reasons the
parties should be able to settle the quantum of costs payable in this file, but
should they be unable to do so, they may refer the issue to an assessment
officer.
[34]
Finally, I have considered Alcon’s suggestion
that Cobalt’s reply submissions constitute improper case-splitting and
determined that, with one exception, they do not. The one exception is Cobalt’s
request to be allowed to file additional materials to address gaps in its
original submission. I am not prepared to allow this as it would amount to case-splitting
and would lead to another protracted round of submissions. To the extent Cobalt
needs to put forth additional materials, it may do so before the assessment
officer. However, I reiterate my hope that the parties ought to be able to
agree on the costs payable now that the parameters have been established in
these Reasons.