AUDREY G. FLEISSIG, District Judge.
This consolidated securities fraud class action is before the Court on Plaintiffs' motion for reconsideration of the scope of the leave to amend their complaint, granted in the Court's Memorandum and Order dated March 27, 2014. For the reasons set forth below, the motion shall be denied, and final judgment shall be entered in favor of Defendants.
Defendants are K-V Pharmaceutical Company and three of its officers (collectively, "K-V"). The putative class of Plaintiffs consists of all purchasers of publically traded securities of K-V between February 14 and April 4, 2011. This litigation is based on allegedly materially false and misleading statements and omissions made by K-V, during the class period, regarding K-V's distribution and sale of the prescription medicine Makena.
As more fully explained in the Court's March 27, 2014 Memorandum and Order, the gravamen of Plaintiff's claims is that K-V knew or should have known that if it charged $1,500 per dose for Makena as planned, the FDA would not enforce K-V's exclusive marketing rights under the Orphan Drug Act ("ODA"), making it impossible for Makena, and in turn K-V, to be commercially successful. According to Plaintiffs, this knowledge rendered both K-V's statements during a February 14, 2011 investor conference call, as well as its failure to mention during the call the likelihood of the FDA's nonenforcement, materially false or misleading in violation of Section 10(b) of the Securities Exchange Act of 1934, as amended by the Private Securities Litigation Reform Act ("PSLRA"), and Rule 10b-5 promulgated thereunder. One of these statements was that K-V would implement a financial assistance program for patients who could not afford Makena at the $1,500 per dose price.
The allegation regarding K-V's knowledge was based in large part on alleged warnings by three confidential witnesses ("CWs") that if K-V charged $1,500 per dose of Makena, the FDA would not enforce K-V's exclusive rights. Indeed, K-V did charge the $1,500 and the FDA did not enforce K-V's exclusive rights, leading to the sharp decline in the value of Plaintiffs' investments in K-V.
The Court concluded that the bulk of K-V's challenged statements were protected by the safe harbor provision of the "PSLRA" because they were forward-looking and accompanied by meaningful cautionary language. Further, with regard to the omission of a statement that there was a risk of nonenforcement of Makena's exclusivity due to the planned price for Makena, the Court concluded that the amended complaint failed sufficiently to plead scienter (a mental state embracing intent to deceive, manipulate, or defraud).
The Court concluded that Plaintiffs' reliance on the CWs' alleged statements to establish K-V's scienter failed because the amended complaint did not allege sufficient facts from which the Court could conclude that the CWs knew or were in a position to know that the FDA would not, or very likely would not, enforce Makena's exclusivity rights. The Court noted that such knowledge on the part of the CWs seemed "improbable in light of the FDA's own statement that its decision was based on a `unique situation.'"
The Court rejected Plaintiffs' suggestion at oral argument that they could possibly further amend their amended complaint to state that the CWs had the requisite knowledge, as follows:
(Doc. No. 116 at 24.)
The Court concluded that K-V's statement about the financial assistance program for patients who could not afford Makena at the planned price was not forward looking, but that the amended complaint was deficient with regard to the falsity of this statement. The Court afforded Plaintiffs leave to file a second amended complaint limited to how this statement was false. The Court granted K-V's motion to dismiss in all other regards.
K-V now asks the Court to reconsider the scope of its leave to amend, seeking the right to amend its allegations with respect to the CWs' knowledge that the FDA would not enforce Makena's exclusivity. The proposed new allegations include that one of the CWs informed K-V that even if the FDA sought to enforce exclusivity, its ability to do so was extremely limited due to its limited resources; that according to CWs that Plaintiffs have re-interviewed or new CWs, no comprehensive market research was conducted by K-V to support the pricing of Makena. Plaintiffs also assert that they are "prepared to provide greater background information on all of the CWs in an amended pleading as well as several new CWs that will demonstrate the CWs had far greater experience and expertise in the area of pharmaceutical marketing, sales and pricing than did the members of K-V management who ignored their warnings" with regard to pricing Makena at $1,500 per dose. (Doc. 119 at 3).
Plaintiffs state that they have no further allegations concerning the financial assistance program and do not intend to amend their allegations in that regard.
Defendants argue that the Court should apply the standard of Federal Rule of Civil Procedure 60(b) to K-V's motion for reconsideration, and deny the motion pursuant to that standard.
Plaintiffs reply that Rule 54(b) applies here, and that reconsideration under that rule is not limited to manifest error or the presentation of previously unavailable evidence. In their reply, Plaintiffs also question the Court's conclusions with respect to whether K-V's statements at issue were forward-looking.
The Court agrees with Plaintiffs that Rule 54(b) applies to Plaintiffs' motion for reconsideration as the Court did not yet direct entry of judgment as to any of Plaintiffs' claims. The standard for reconsideration under Rule 54(b) is not entirely clear. Some courts have expressed the lenient standard urged by Plaintiffs. See, e.g., United States v. Renda, 709 F.3d 472, 479 (5th Cir. 2013) ("Rule 54(b) authorizes a district court to reconsider and reverse its prior rulings on any interlocutory order for any reason it deems sufficient."). But in this Circuit and District the standard is stricter, such that a Rule 54(b) motion for reconsideration "may not serve as a vehicle to identify facts or raise legal arguments which could have been, but were not, raised or adduced during the pendency of the motion of which reconsideration was sought." See Evans v. Contract Callers, Inc., No. 4:10CV02358 FRB, 2012 WL 234653, at *2 (E.D. Mo. Jan. 25, 2012) (citation omitted); see also Chism v. W.R. Grace & Co., 158 F.3d 988, 992 n.4 (8th Cir. 1998); Evans v. Contract Callers, Inc., No. 4:10CV2358 FRB, 2012 WL 234653, at *2 (E.D. Mo. Jan. 25, 2012) ("Although the Court has the power [under Rule 54(b)] to revisit prior decisions of its own . . . [it] should be loathe to do so in the absence of extraordinary circumstances such as where the initial decision was clearly erroneous and would work a manifest injustice.").
Here, under either standard for a Rule 54(b) motion, Plaintiffs' motion fails. The Court gave careful consideration to the legal arguments Plaintiffs presented earlier in opposition to K-V's motion to dismiss, and again now for reconsideration. None of Plaintiffs' arguments for reconsideration are deemed sufficient by the Court. And though the Court granted Plaintiffs leave to amend with respect to the financial assistance program, they say they do not intend to amend in this regard. Thus, it appears that it is time for the Eighth Circuit Court of Appeals to consider the Court's rulings, should Plaintiffs choose to file an appeal.
Accordingly,
A separate Judgment shall accompany this Memorandum and Order.