OPINION OF THE COURT
MERCK & CO. V. REYNOLDS
559 U. S. ____ (2010)
SUPREME COURT OF THE UNITED STATES
NO. 08-905
MERCK & CO., INC., et al., PETITIONERS
v. RICHARD REYNOLDS et al.
on writ of certiorari to the united states court of
appeals for the third circuit
[April 27, 2010]
Justice Breyer delivered the
opinion of the Court.
This case concerns the timeliness
of a complaint filed in a private securities fraud action. The
complaint was timely if filed no more than two years after the
plaintiffs “discover[ed] the facts constituting the violation.” 28
U. S. C. §1658(b)(1). Construing this limitations statute for
the first time, we hold that a cause of action accrues (1) when the
plaintiff did in fact discover, or (2) when a reasonably diligent
plaintiff would have discovered, “the facts constituting the
violation”—whichever comes first. We also hold that the “facts
constituting the violation” include the fact of scienter, “a mental
state embracing intent to deceive, manipulate, or defraud,”
Ernst & Ernst v.
Hochfelder,
425 U. S. 185, 194,
n. 12 (1976). Applying this standard, we affirm the Court of
Appeals’ determination that the complaint filed here was
timely.
I
The action before us involves a
claim by a group of investors (the plaintiffs, respondents here)
that Merck & Co. and others (the petitioners here, hereinafter
Merck) knowingly misrepresented the risks of heart attacks
accompanying the use of Merck’s pain-killing drug, Vioxx (leading
to economic losses when the risks later became apparent). The
plaintiffs brought an action for securities fraud under §10(b) of
the Securities Exchange Act of 1934. See 48 Stat. 891, as amended,
15 U. S. C. §78j(b); SEC Rule 10b–5, 17 CFR §240.10b–5(b)
(2009);
Dura Pharmaceuticals, Inc. v.
Broudo,
544 U. S. 336,
341–342 (2005).
The applicable statute of
limitations provides that a “private right of action” that, like
the present action, “involves a claim of fraud, deceit,
manipulation, or contrivance in contravention of a regulatory
requirement concerning the securities laws … may be brought not
later than the earlier of—
“(1) 2 years after the discovery of the facts
constituting the violation; or
“(2) 5 years after such violation.” 28 U.
S. C. §1658(b).
The complaint in this case was filed on
November 6, 2003, and no one doubts that it was filed within five
years of the alleged violation. Therefore, the critical date for
timeliness purposes is November 6, 2001—two years before this
complaint was filed. Merck claims that before this date the
plaintiffs had (or should have) discovered the “facts constituting
the violation.” If so, by the time the plaintiffs filed their
complaint, the 2-year statutory period in §1658(b)(1) had run. The
plaintiffs reply that they had not, and could not have, discovered
by the critical date those “facts,” particularly not the facts
related to scienter, and that their complaint was therefore
timely.
A
We first set out the relevant
pre-November 2001 facts, as we have gleaned them from the briefs,
the record, and the opinions below.
1. 1990’s. In
the mid-1990’s Merck developed Vioxx. In 1999 the Food and Drug
Administration (FDA) approved it for prescription use. Vioxx
suppresses pain by inhibiting the body’s production of an enzyme
called COX–2 (cyclooxygenase-2). COX–2 is associated with pain and
inflammation. Unlike some other anti-inflammatory drugs in its
class like aspirin, ibuprofen, and naproxen, Vioxx does not inhibit
production of a second enzyme called COX–1 (cyclooxygenase-1).
COX–1 plays a part in the functioning of the gastrointestinal tract
and also inhibits platelet aggregation (associated with blood
clots). App. 50–51.
2. March 2000. Merck
announced the results of a study, called the “VIGOR” study.
Id., at 291–294. The study compared Vioxx with another
painkiller, naproxen. The study showed that persons taking Vioxx
suffered fewer gastrointestinal side effects (as Merck had hoped).
But the study also revealed that approximately 4 out of every 1,000
participants who took Vioxx suffered heart attacks, compared to
only 1 per 1,000 participants who took naproxen.
Id., at
296, 306; see Bombardier et al., Comparison of Upper
Gastrointestinal Toxicity of Rofecoxib and Naproxen in Patients
with Rheumatoid Arthritis, 343 New England J. Medicine 1520, 1523,
1526–1527 (2000).
Merck’s press release acknowledged VIGOR’s
adverse cardiovascular data. But Merck said that these data were
“consistent with naproxen’s ability to block platelet aggregation.”
App. 291. Merck noted that, since “Vioxx, like all COX–2 selective
medicines, does not block platelet aggregation[, it] would not be
expected to have similar effects.”
Ibid. And Merck added
that “safety data from all other completed and ongoing clinical
trials … showed no indication of a difference in the incidence of
thromboembolic events between Vioxx” and either a placebo or
comparable drugs.
Id., at 293 (emphasis deleted).
This theory—that VIGOR’s troubling
cardiovascular findings might be due to the absence of a benefit
conferred by naproxen rather than due to a harm caused by
Vioxx—later became known as the “naproxen hypothesis.” In advancing
that hypothesis, Merck acknowledged that the naproxen benefit “had
not been observed previously.”
Id., at 291. Journalists
and stock market analysts reported all of the above—the positive
gastrointestinal results, the troubling cardiovascular finding, the
naproxen hypothesis, and the fact that the naproxen hypothesis was
unproved. See
id., at 355–391, 508–557.
3. February 2001 to August
2001. Public debate about the naproxen hypothesis continued.
In February 2001, the FDA’s Arthritis Advisory Committee convened
to consider Merck’s request that the Vioxx label be changed to
reflect VIGOR’s positive gastrointestinal findings. The VIGOR
cardiovascular findings were also discussed.
Id., at
392–395, 558–577. In May 2001, a group of plaintiffs filed a
products-liability lawsuit against Merck, claiming that “Merck’s
own research” had demonstrated that “users of Vioxx were four times
as likely to suffer heart attacks as compared to other less
expensive, medications.”
Id., at 869. In August 2001, the
Journal of the American Medical Association wrote that the
available data raised a “cautionary flag” and strongly urged that
“a trial specifically assessing cardiovascular risk” be done.
Id., at 331–332; Mukherjee, Nissen, & Topol, Risk of
Cardiovascular Events Associated with Selective Cox-2 Inhibitors,
286 JAMA 954 (2001). At about the same time, Bloomberg News quoted
a Merck scientist who claimed that Merck had “additional data” that
were “very, very reassuring,” and Merck issued a press release
stating that it stood “behind the overall and cardiovascular safety
profile … of Vioxx.” App. 434, 120 (emphasis deleted; internal
quotation marks omitted).
4. September and October
2001. The FDA sent Merck a warning letter released to the
public on September 21, 2001. It said that, in respect to
cardiovascular risks, Merck’s Vioxx marketing was “false, lacking
in fair balance, or otherwise misleading.”
Id., at 339. At
the same time, the FDA acknowledged that the naproxen hypothesis
was a “possible explanation” of the VIGOR results.
Id., at
340. But it found that Merck’s “promotional campaign selectively
present[ed]” that hypothesis without adequately acknowledging
“another reasonable explanation,” namely, “that Vioxx may have
pro-thrombotic [
i.e., adverse cardiovascular] properties.”
Ibid. The FDA ordered Merck to send healthcare providers a
corrective letter.
Id., at 353.
After the FDA letter was released, more
products-liability lawsuits were filed. See
id., at
885–956. Merck’s share price fell by 6.6% over several days. See
id., at 832. By October 1, the price rebounded. See
ibid. On October 9, 2001, the New York Times said that
Merck had reexamined its own data and “found no evidence that Vioxx
increased the risk of heart attacks.” App. 504. It quoted the
president of Merck Research Laboratories as positing “ ‘two
possible interpretations’ ”: “ ‘Naproxen lowers the heart
attack rate, or Vioxx raises it.’ ”
Ibid. Stock
analysts, while reporting the warning letter, also noted that the
FDA had not denied that the naproxen hypothesis remained an
unproven but possible explanation. See
id., at 614, 626,
628.
B
We next set forth three important
events that occurred
after the critical date.
1. October 2003. The
Wall Street Journal published the results of a Merck-funded Vioxx
study conducted at Boston’s Brigham and Women’s Hospital. After
examining the medical records of more than 50,000 Medicare
patients, researchers found that those given Vioxx for 30-to-90
days were 37% more likely to have suffered a heart attack than
those given either a different painkiller or no painkiller at
all
. Id., at 164–165. (That is to say, if
patients given a different painkiller or given no painkiller at all
suffered 10 heart attacks, then the same number of patients given
Vioxx would suffer 13 or 14 heart attacks.) Merck defended Vioxx
and pointed to the study’s limitations.
Id., at
165–167.
2. September 30, 2004. Merck
withdrew Vioxx from the market. It said that a new study had found
“an increased risk of confirmed cardiovascular events beginning
after 18 months of continuous therapy.”
Id., at 182
(internal quotation marks omitted). A Merck representative publicly
described the results as “totally unexpected.”
Id., at
186. Merck’s shares fell by 27% the same day.
Id., at 185,
856.
3. November 1, 2004. The
Wall Street Journal published an article stating that “internal
Merck e-mails and marketing materials as well as interviews with
outside scientists show that the company fought forcefully for
years to keep safety concerns from destroying the drug’s commercial
prospects.”
Id., at 189–190. The article said that an
early e-mail from Merck’s head of research had said that the VIGOR
“results showed that the cardiovascular events ‘are clearly
there,’ ” that it was “ ‘a shame but … a low
incidence,’ ” and that it “ ‘is mechanism based as we
worried it was.’ ”
Id., at 192. It also said that
Merck had given its salespeople instructions to
“ ‘DODGE’ ” questions about Vioxx’s cardiovascular
effects.
Id., at 193.
C
The plaintiffs filed their
complaint on November 6, 2003. As subsequently amended, the
complaint alleged that Merck had defrauded investors by promoting
the naproxen hypothesis, knowing the hypothesis was false. It said,
for example, that Merck “knew, at least as early as 1996, of the
serious safety issues with Vioxx,” and that a “1998 internal Merck
clinical trial … revealed that … serious cardiovascular events …
occurred six times more frequently in patients given Vioxx than in
patients given a different arthritis drug or placebo.”
Id., at 56, 58–59 (emphasis and capitalization
deleted).
Merck, believing that the
plaintiffs knew or should have known the “facts constituting the
violation” at least two years earlier, moved to dismiss the
complaint, saying it was filed too late. The District Court granted
the motion. The court held that the (March 2001) VIGOR study, the
(September 2001) FDA warning letter, and Merck’s (October 2001)
response should have alerted the plaintiffs to a
“possibility that Merck had knowingly misrepresented
material facts” no later than October 9, 2001, thus placing the
plaintiffs on “inquiry notice” to look further.
In re
Merck & Co. Securities, Derivative & “ERISA”
Litigation, 483 F. Supp. 2d 407, 423 (NJ 2007) (emphasis
added). Finding that the plaintiffs had failed to “show that they
exercised reasonable due diligence but nevertheless were unable to
discover their injuries,” the court took October 9, 2001, as the
date that the limitations period began to run and therefore found
the complaint untimely.
Id., at 424.
The Court of Appeals for the Third Circuit
reversed. A majority held that the pre-November 2001 events, while
constituting “storm warnings,” did not suggest much by way of
scienter, and consequently did not put the plaintiffs on “inquiry
notice,” requiring them to investigate further.
In re
Merck & Co. Securities, Derivative & “ERISA”
Litigation, 543 F. 3d 150, 172 (2008). A dissenting judge
considered the pre-November 2001 events sufficient to start the
2-year clock running.
Id., at 173 (opinion of Roth,
J.).
Merck sought review in this Court, pointing to
disagreements among the Courts of Appeals. Compare
Theoharous v.
Fong, 256 F. 3d 1219, 1228
(CA11 2001) (limitations period begins to run when information puts
plaintiffs on “inquiry notice” of the need for investigation), with
Shah v.
Meeker, 435 F. 3d 244, 249 (CA2
2006) (same; but if plaintiff
does investigate, period
runs “from the date such inquiry should have revealed the fraud”
(internal quotation marks omitted)), and
New England Health
Care Employees Pension Fund v.
Ernst & Young,
LLP, 336 F. 3d 495, 501 (CA6 2003) (limitations period
always begins to run only when a reasonably diligent
plaintiff, after being put on “inquiry notice,” should have
discovered facts constituting violation (internal quotation marks
omitted)). We granted Merck’s petition.
II
Before turning to Merck’s
arguments, we consider a more basic matter. The parties and the
Solicitor General agree that §1658(b)(1)’s word “discovery” refers
not only to a plaintiff’s
actual discovery of certain
facts, but also to the facts that a reasonably diligent plaintiff
would have discovered. We agree. But because the statute’s language
does not make this interpretation obvious, and because we cannot
answer the question presented without considering whether the
parties are right about this matter, we set forth the reasons for
our agreement in some detail.
We recognize that one might read
the statutory words “after the discovery of the facts constituting
the violation” as referring to the time a plaintiff
actually discovered the relevant facts. But in the statute
of limitations context, the word “discovery” is often used as a
term of art in connection with the “discovery rule,” a doctrine
that delays accrual of a cause of action until the plaintiff has
“discovered” it. The rule arose in fraud cases as an exception to
the general limitations rule that a cause of action accrues once a
plaintiff has a “complete and present cause of action,”
Bay
Area Laundry and Dry Cleaning Pension Trust Fund v.
Ferbar
Corp. of Cal.,
522 U. S. 192, 201
(1997) (citing
Clark v.
Iowa City, 20 Wall. 583,
589 (1875); internal quotation marks omitted). This Court long ago
recognized that something different was needed in the case of
fraud, where a defendant’s deceptive conduct may prevent a
plaintiff from even
knowing that he or she has been
defrauded. Otherwise, “the law which was designed to prevent fraud”
could become “the means by which it is made successful and secure.”
Bailey v.
Glover, 21 Wall. 342, 349 (1875).
Accordingly, “where a plaintiff has been injured by fraud and
remains in ignorance of it without any fault or want of diligence
or care on his part, the bar of the statute does not begin to run
until the fraud is
discovered.”
Holmberg v.
Armbrecht,
327 U. S. 392, 397
(1946) (internal quotation marks omitted; emphasis added). And for
more than a century, courts have understood that “[f]raud is deemed
to be discovered . . . when, in the exercise of reasonable
diligence, it could have been discovered.” 2 H. Wood, Limitation of
Actions §276b(11), p. 1402 (4th ed. 1916); see
id., at
1401–1403, and nn. 74–84 (collecting cases and statutes); see,
e.g., Holmberg, supra, at 397;
Kirby v.
Lake Shore & Michigan Southern R. Co.,
120 U. S. 130, 138
(1887) (The rule “regard[s] the cause of action as having accrued
at the time the fraud was or should have been discovered”).
More recently, both state and federal courts
have applied forms of the “discovery rule” to claims other than
fraud. See 2 C. Corman, Limitation of Actions §§11.1.2.1, 11.1.2.3,
pp. 136–142, and nn. 6–13, 18–23 (1991 and 1993 Supp.) (hereinafter
Corman) (collecting cases); see,
e.g., United
States v.
Kubrick,
444 U. S. 111 (1979).
Legislatures have codified the discovery rule in various contexts.
2 Corman §11.2, at 170–171, and nn. 1–9 (collecting statutes); see,
e.g., 28 U. S. C. §2409a(g) (actions to quiet title
against the United States). In doing so, legislators have written
the word “discovery” directly into the statute. And when they have
done so, state and federal courts have typically interpreted the
word to refer not only to actual discovery, but also to the
hypothetical discovery of facts a reasonably diligent plaintiff
would know. See,
e.g., Peacock v.
Barnes, 142 N. C. 215, 217–220, 55 S. E. 99, 100
(1906);
Davis v.
Hibernia Sav. & Loan Soc.,
21 Cal. App. 444, 448, 132 P. 462, 464 (1913);
Roether v.
National Union Fire Ins. Co., 51 N. D. 634, 640–642,
200 N. W. 818, 821 (1924);
Goldenberg v.
Bache
& Co., 270 F. 2d 675, 681 (CA5 1959);
Mobley
v.
Hall, 202 Mont. 227, 232, 657 P. 2d 604, 606
(1983);
Tregenza v.
Great American Communications
Co., 12 F. 3d 717, 721–722 (CA7 1993);
J. Geils Band
Employee Benefit Plan v.
Smith Barney Shearson, Inc.,
76 F. 3d 1245, 1254 (CA1 1996).
Thus, treatise writers now describe “the
discovery rule” as allowing a claim “to accrue when the litigant
first knows
or with due diligence should know facts that
will form the basis for an action.” 2 Corman §11.1.1, at 134
(emphasis added); see also
ibid., n. 1 (collecting
cases); 37 Am. Jur. 2d, Fraud and Deceit §347, p. 354 (2001 and
Supp. 2009) (noting that the various formulations of “discovery”
all provide that “in addition to actual knowledge of the fraud,
once a reasonably diligent party is in a position that they should
have sufficient knowledge or information to have actually
discovered the fraud, they are charged with discovery”);
id., at 354–355, and nn. 2–11 (collecting cases).
Like the parties, we believe that Congress
intended courts to interpret the word “discovery” in §1658(b)(1)
similarly. Before Congress enacted that statute, this Court, having
found in the federal securities laws the existence of an implied
private §10(b) action, determined its governing limitations period
by looking to other limitations periods in the federal securities
laws.
Lampf, Pleva, Lipkind, Prupis & Petigrow v.
Gilbertson,
501 U. S. 350 (1991).
Noting the existence of various formulations “differ[ing] slightly
in terminology,” the Court chose the language in 15 U. S. C.
§78i(e), the statutory provision that governs securities price
manipulation claims. 501 U. S.
, at 364, n. 9. And in
doing so, the Court said that private §10(b) actions “must be
commenced within one year
after the discovery of the facts
constituting the violation and within three years after such
violation.”
Id., at 364 (emphasis added). (The Court
listed among the various formulations the one in 15 U. S. C.
§77m, on which the concurrence relies. See
post, at 2–4
(Scalia, J., concurring in part and concurring in judgment);
Lampf,
supra, at 360, and n. 7 (quoting
§77m).)
Subsequently, every Court of Appeals to decide
the matter held that “discovery of the facts constituting the
violation” occurs not only once a plaintiff
actually
discovers the facts, but also when a hypothetical reasonably
diligent plaintiff would have discovered them. See,
e.g.,
Law v.
Medco Research, Inc., 113 F. 3d 781,
785–786 (CA7 1997);
Dodds v.
Cigna Securities,
Inc., 12 F. 3d 346, 350, 353 (CA2 1993); see
In re NAHC, Inc. Securities Litigation, 306
F. 3d 1314, 1325, n. 4 (CA3 2002) (collecting cases).
Some of those courts noted that other limitations provisions in the
federal securities laws explicitly provide that the period begins
to run “ ‘after the discovery of the untrue statement …
or after such discovery should have been made by [the]
exercise of reasonable diligence,’ ” whereas the
formulation adopted by the Court in
Lampf from 15 U.
S. C. §78i(e) does not.
Tregenza,
supra, at
721 (quoting §77m; emphasis added in
Tregenza); see
Lampf,
supra, at 364, n. 9. But, courts
reasoned, because the term “discovery” in respect to statutes of
limitations for fraud has long been understood to include
discoveries a reasonably diligent plaintiff would make, the
omission of an explicit provision to that effect did not matter.
Tregenza,
supra, at 721; accord,
New England
Health Care, 336 F. 3d, at 499–500.
In 2002, when Congress enacted the present
limitations statute, it repeated
Lampf’s critical
language. The statute says that an action based on fraud “may be
brought not later than the earlier of … 2 years
after the
discovery of the facts constituting the violation” (or “5
years after such violation”). §804 of the Sarbanes-Oxley Act, 116
Stat. 801, codified at 28 U. S. C. §1658(b) (emphasis added).
(This statutory provision does
not make the linguistic
distinction that the concurrence finds in a
different
statute, §77m, and upon which its argument rests. Cf. 29 U.
S. C. §1113(2) (statute in which Congress provided that an
action be brought “three years after the earliest date on which the
plaintiff had
actual knowledge of the breach or violation”
(emphasis added)).) Not surprisingly, the Courts of Appeals
unanimously have continued to interpret the word “discovery” in
this statute as including not only facts a particular plaintiff
knows, but also the facts any reasonably diligent plaintiff would
know
. See,
e.g., Staehr v.
Hartford
Financial Servs. Group, Inc., 547 F. 3d 406, 411 (CA2
2008);
Sudo Properties, Inc. v.
Terrebonne Parish
Consolidated Govt., 503 F. 3d 371, 376 (CA5 2007).
We normally assume that, when Congress enacts
statutes, it is aware of relevant judicial precedent. See,
e.g., Edelman v.
Lynchburg College,
535 U. S. 106,
116–117, and n. 13 (2002);
Commissioner v.
Keystone Consol. Industries, Inc.,
508 U. S. 152, 159
(1993). Given the history and precedent surrounding the use of the
word “discovery” in the limitations context generally as well as in
this provision in particular, the reasons for making this
assumption are particularly strong here. We consequently hold that
“discovery” as used in this statute encompasses not only those
facts the plaintiff actually knew, but also those facts a
reasonably diligent plaintiff would have known. And we evaluate
Merck’s claims accordingly.
III
We turn now to Merck’s arguments
in favor of holding that petitioners’ claims accrued before
November 6, 2001. First, Merck argues that the statute does not
require “discovery” of scienter-related “facts.” See Brief for
Petitioners 19–28. We cannot agree, however, that facts about
scienter are unnecessary.
The statute says that the
limitations period does not begin to run until “discovery of the
facts constituting the violation.” 28 U. S. C.
§1658(b)(1) (emphasis added). Scienter is assuredly a “fact.” In a
§10(b) action, scienter refers to “a mental state embracing intent
to deceive, manipulate, or defraud.”
Ernst & Ernst,
425 U. S., at 194, n. 12. And the “ ‘state of a man’s
mind is as much a fact as the state of his digestion.’ ”
Postal Service Bd. of Governors v.
Aikens,
460 U. S. 711,
716 (1983) (quoting
Edgington v.
Fitzmaurice,
[1885] 29 Ch. Div. 459, 483).
And this “fact” of scienter “constitut[es]” an
important and necessary element of a §10(b) “violation.” A
plaintiff cannot recover without proving that a defendant made a
material misstatement
with an intent to deceive—not merely
innocently or negligently. See
Tellabs, Inc. v.
Makor
Issues & Rights, Ltd.,
551 U. S. 308, 319
(2007);
Ernst & Ernst,
supra. Indeed,
Congress has enacted special heightened pleading requirements for
the scienter element of §10(b) fraud cases. See 15 U. S. C.
§78u–4(b)(2) (requiring plaintiffs to “state with particularity
facts giving rise to a strong inference that the defendant
acted with the required state of mind” (emphasis added)). As a
result, unless a §10(b) plaintiff can set forth facts in the
complaint showing that it is more likely than not that the
defendant acted with the relevant knowledge or intent, the claim
will fail. See
Tellabs,
supra, at 328. It would
therefore frustrate the very purpose of the discovery rule in this
provision—which, after all, specifically applies only in cases
“involv[ing] a claim of fraud, deceit, manipulation, or
contrivance,” §1658(b)—if the limitations period began to run
regardless of whether a plaintiff had discovered any facts
suggesting scienter. So long as a defendant concealed for two years
that he made a misstatement with an intent to deceive, the
limitations period would expire before the plaintiff had actually
“discover[ed]” the fraud.
We consequently hold that facts showing
scienter are among those that “constitut[e] the violation.” In so
holding, we say nothing about other facts necessary to support a
private §10(b) action. Cf. Brief for United States as
Amicus
Curiae 12, n. 1 (suggesting that facts concerning a
plaintiff’s reliance, loss, and loss causation are not among those
that constitute “the violation” and therefore need not be
“discover[ed]” for a claim to accrue).
Second, Merck argues that, even if “discovery”
requires facts related to scienter, facts that tend to show a
materially false or misleading statement (or material omission) are
ordinarily sufficient to show scienter as well. See Brief for
Petitioners 22, 28–29. But we do not see how that is so. We
recognize that certain statements are such that, to show them false
is normally to show scienter as well. It is unlikely, for example,
that someone would falsely say “I am not married” without being
aware of the fact that his statement is false. Where §10(b) is at
issue, however, the relation of factual falsity and state of mind
is more context specific. An incorrect prediction about a firm’s
future earnings, by itself, does not automatically tell us whether
the speaker deliberately lied or just made an innocent (and
therefore nonactionable) error. Hence, the statute may require
“discovery” of scienter-related facts beyond the facts that show a
statement (or omission) to be materially false or misleading. Merck
fears that this requirement will give life to stale claims or
subject defendants to liability for acts taken long ago. But
Congress’ inclusion in the statute of an unqualified bar on actions
instituted “5 years after such violation,” §1658(b)(2), giving
defendants total repose after five years, should diminish that
fear. Cf.
Lampf, 501 U. S., at 363 (holding comparable bar
not subject to equitable tolling).
Third, Merck says that the limitations period
began to run prior to November 2001 because by that point the
plaintiffs were on “inquiry notice.” Merck uses the term “inquiry
notice” to refer to the point “at which a plaintiff possesses a
quantum of information sufficiently suggestive of wrongdoing that
he should conduct a further inquiry.” Brief for Petitioners 20. And
some, but not all, Courts of Appeals have used the term in roughly
similar ways. See,
e.g., Franze v.
Equitable
Assurance, 296 F. 3d 1250, 1254 (CA11 2002) (“[I]nquiry
notice [is] “ ‘the term used for knowledge of facts that would
lead a reasonable person to begin investigating the possibility
that his legal rights had been infringed’ ”). Cf.
Dodds, 12 F. 3d, at 350 (“duty of inquiry” arises
once “circumstances would suggest to an investor of ordinary
intelligence the probability that she had been defrauded”);
Fujisawa Pharmaceutical Co. v.
Kapoor, 115
F. 3d 1332, 1335–1336 (CA7 1997) (“The facts constituting
[inquiry] notice must be sufficien[t] … to incite the victim to
investigate” and “to enable him to tie up any loose ends and
complete the investigation in time to file a timely suit”);
Great Rivers Cooperative of Southeastern Iowa v.
Farmland Industries, Inc., 120 F. 3d 893, 896 (CA8
1997) (“Inquiry notice exists when the victim is aware of facts
that would lead a reasonable person to investigate
and
consequently acquire actual knowledge of the defendant’s
misrepresentations” (emphasis added)).
If the term “inquiry notice” refers to the
point where the facts would lead a reasonably diligent plaintiff to
investigate further, that point is not necessarily the point at
which the plaintiff would already have discovered facts showing
scienter or other “facts constituting the violation.” But the
statute says that the plaintiff’s claim accrues only after the
“discovery” of those latter facts. Nothing in the text suggests
that the limitations period can sometimes begin
before
“discovery” can take place. Merck points out that, as we have
discussed, see
supra, at 8–9, the court-created “discovery
rule” exception to ordinary statutes of limitations is not
generally available to plaintiffs who fail to pursue their claims
with reasonable diligence. But we are dealing here with a statute,
not a court-created exception to a statute. Because the statute
contains no indication that the limitations period should occur at
some earlier moment before “discovery,” when a plaintiff would have
begun investigating, we cannot accept Merck’s
argument.
As a fallback, Merck argues that even if the
limitations period does generally begin at “discovery,” it should
nonetheless run from the point of “inquiry notice” in one
particular situation, namely, where the actual plaintiff fails to
undertake an investigation once placed on “inquiry notice.” In such
circumstances, Merck contends, the actual plaintiff is not
diligent, and the law should not “effectively excuse a plaintiff’s
failure to conduct a further investigation” by placing that
nondiligent plaintiff and a reasonably diligent plaintiff “in the
same position.” Brief for Petitioners 48.
We cannot accept this argument for essentially
the same reason we reject “inquiry notice” as the standard
generally: We cannot reconcile it with the statute, which simply
provides that “discovery” is the event that triggers the 2-year
limitations period—for all plaintiffs. Cf.
United States
v.
Mack,
295 U. S. 480, 489
(1935) (“Laches within the term of the statute of limitations is no
defense at law”). Furthermore, the statute does
not place
all plaintiffs “in the same position” no matter whether they
investigate when investigation is warranted. The limitations period
puts plaintiffs who fail to investigate once on “inquiry notice” at
a disadvantage because it lapses two years after a reasonably
diligent plaintiff would have discovered the necessary facts. A
plaintiff who fails entirely to investigate or delays investigating
may well not have discovered those facts by that time or, at least,
may not have found sufficient facts by that time to be able to file
a §10(b) complaint that satisfies the applicable heightened
pleading standards. Cf.
Young v.
Lepone, 305
F. 3d 1, 9 (CA1 2002) (“[A] reasonably diligent investigation
… may consume as little as a few days or as much as a few years to
get to the bottom of the matter”).
Merck further contends that its proposed
“inquiry notice” standard is superior, because determining when a
hypothetical reasonably diligent plaintiff would have
“discover[ed]” the necessary facts is too complicated for judges to
undertake. But courts applying the traditional discovery rule have
long had to ask what a reasonably diligent plaintiff would have
known and done in myriad circumstances. And courts in at least five
Circuits already ask this kind of question in securities fraud
cases. See,
e.g.,
Rothman v.
Gregor, 220
F. 3d 81, 97 (CA2 2000);
New England Health Care, 336
F. 3d, at 501;
Young, supra, at 1, 9–10;
Sterlin v.
Biomune Systems, 154 F. 3d 1191,
1201 (CA10 1998);
Marks v.
CDW Computer Centers,
Inc., 122 F. 3d 363, 367–368 (CA7 1997). Merck has not
shown this precedent to be unworkable. We consequently find that
the “discovery” of facts that put a plaintiff on “inquiry notice”
does not automatically begin the running of the limitations
period.
We conclude that the limitations period in
§1658(b)(1) begins to run once the plaintiff did discover or a
reasonably diligent plaintiff would have “discover[ed] the facts
constituting the violation”—whichever comes first. In determining
the time at which “discovery” of those “facts” occurred, terms such
as “inquiry notice” and “storm warnings” may be useful to the
extent that they identify a time when the facts would have prompted
a reasonably diligent plaintiff to begin investigating. But the
limitations period does not begin to run until the plaintiff
thereafter discovers or a reasonably diligent plaintiff would have
discovered “the facts constituting the violation,” including
scienter—irrespective of whether the actual plaintiff undertook a
reasonably diligent investigation.
IV
Finally, Merck argues that, even
if all its other legal arguments fail, the record still shows that,
before November 6, 2001, the plaintiffs had discovered or should
have discovered “the facts constituting the violation.” In respect
to scienter Merck primarily relies upon (1) the FDA’s September
2001 warning letter, which said that Merck had
“ ‘minimized’ ” the VIGOR study’s “ ‘potentially
serious cardiovascular findings’ ” and (2) pleadings filed in
products-liability actions in September and October 2001 alleging
that Merck had “ ‘omitted, suppressed, or concealed material
facts concerning the dangers and risks associated with
Vioxx’ ” and “
purposefully downplayed and/or
understated the serious nature of the risks associated with Vioxx.”
Brief for Petitioners 36–37 (quoting App. 340, 893).
The FDA’s warning letter,
however, shows little or nothing about the here-relevant scienter,
i.e., whether Merck advanced the naproxen hypothesis with
fraudulent intent. See Part I–A
(4),
supra. The
FDA itself described the pro-Vioxx naproxen hypothesis as a
“possible explanation” for the VIGOR results, faulting Merck only
for failing sufficiently to publicize the alternative less
favorable to Merck, that Vioxx might be harmful. App. 340.
The products-liability complaints’ statements
about Merck’s knowledge show little more. See Part I–A
(3),
supra. Merck does not claim that these complaints
contained any specific information suggesting the fraud alleged
here,
i.e., that Merck knew the naproxen hypothesis was
false even as it promoted it. And, without providing any reason to
believe that the plaintiffs had special access to information about
Merck’s state of mind, the complaints alleged only in general terms
that Merck had concealed information about Vioxx and “purposefully
downplayed and/or understated” the risks associated with Vioxx—the
same charge made in the FDA warning letter. App. 893.
In our view, neither these two circumstances
nor any of the other pre-November 2001 circumstances that we have
set forth in Part I–A,
supra, whether viewed separately or
together, reveal “facts” indicating scienter. Regardless of which,
if any, of the events following November 6, 2001, constituted
“discovery,” we need only conclude that prior to November 6, 2001,
the plaintiffs did not discover, and Merck has not shown that a
reasonably diligent plaintiff would have discovered, “the facts
constituting the violation.” In light of our interpretation of the
statute, our holdings in respect to scienter, and our application
of those holdings to the circumstances of this case, we must, and
we do, reach that conclusion. Thus, the plaintiffs’ suit is timely.
We need not—and do not—pass upon the Court of Appeals’ suggestion
that the November 2003 Brigham and Women’s study might have
triggered the statute of limitations. The judgment of the Court of
Appeals is
Affirmed.
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