Cell Therapeutics Inc v. Lash Group Inc

Procedural entryThis page is a short order in Cell Therapeutics Inc v. Lash Group Inc. Read the opinion of the Court — 586 F.3d 1204
Court of Appeals for the Ninth Circuit·Decided November 18, 2009·No. 08-35619·Published

Opinion

FOR PUBLICATION UNITED STATES COURT OF APPEALS FOR THE NINTH CIRCUIT

CELL THERAPEUTICS INC.,  Plaintiff-Appellant, No. 08-35619 v.  D.C. No. 2:07-cv-00310-JLR LASH GROUP INC.; DOCUMEDICS ACQUISITION CO., INC., OPINION Defendants-Appellees.  Appeal from the United States District Court for the Western District of Washington James L. Robart, District Judge, Presiding

Argued and Submitted August 31, 2009—Seattle, Washington

Filed November 18, 2009

Before: Michael Daly Hawkins, M. Margaret McKeown and Jay S. Bybee, Circuit Judges.

Opinion by Judge McKeown

15303 15306 CELL THERAPEUTICS v. LASH GROUP

COUNSEL

Daniel J. Dunne and Paul F. Rugani, Orrick, Herrington & Sutcliffe LLP, Seattle, Washington, for the appellant.

Raymond A. Cardozo, Reed Smith LLP, San Francisco, Cali- fornia, and Laurie M. Thornton, Corr Cronin Michelson Baumgardner & Preece LLP, Seattle, Washington, for the appellee.

OPINION

McKEOWN, Circuit Judge:

The False Claims Act (“FCA”) was designed to encourage reporting of false or fraudulent claims that are submitted to the federal government for approval or payment. Typically a relator—a whistle-blowing employee, a business partner or competitor—brings suit “for the benefit of the United States.” Mortgages, Inc. v. U.S. Dist. Ct., 934 F.2d 209, 210 (9th Cir. 1991) (per curiam). The government has discretion to inter- vene in the suit as a plaintiff. But what happens when a target CELL THERAPEUTICS v. LASH GROUP 15307 defendant settles with the government and the relator and then seeks recovery against a third party for contractual indemnity and independent claims? We have not previously had occa- sion to address this question. We conclude that the FCA does not preclude such claims.

I. BACKGROUND

A. THE FALSE CLAIMS ACT

A brief review of the Act’s structure is useful in putting the third party claim issue in context. The purpose of the FCA is “to discourage fraud against the government.” Robertson v. Bell Helicopter Textron, Inc., 32 F.3d 948, 951 (5th Cir. 1994). The FCA imposes civil liability on any person who knowingly uses a “false record or statement to get a false or fraudulent claim paid or approved by the Government,” 31 U.S.C. § 3729(a)(2) (1984), and any person who “conspires to defraud the Government by getting a false or fraudulent claim allowed or paid.” Id. § 3729(a)(3).1 To encourage the disclo- sure of potential fraud, under the qui tam provisions of the FCA, relators may “bring a civil action for a violation of [§ ] 3729 for the person and for the United States Government.” Id. § 3730(b)(1); United States ex rel. Hall v. Teledyne Wah Chang Albany, 104 F.3d 230, 233 (9th Cir. 1997). If the gov- ernment does not intervene in the suit, the relator may pro- ceed with the FCA litigation. 31 U.S.C. § 3730(c)(3). If the government elects to intervene, the relator remains part of the suit as a qui tam plaintiff, id. § 3730(b)(2), but the govern- 1 The statute was recently amended and now holds liable “any person who knowingly presents, or causes to be presented, a false or fraudulent claim for payment or approval; knowingly makes, uses, or causes to be made or used, a false record or statement material to a false or fraudulent claim; [or] conspires to commit a violation of” these subparagraphs. 31 U.S.C. § 3729(a)(1)(A)-(C) (effective May 20, 2009). CTI was charged under the prior language, but the differences are not material to our deci- sion. 15308 CELL THERAPEUTICS v. LASH GROUP ment may dismiss or settle the action over the relator’s objec- tion. Id. § 3730(c)(2)(A)-(B).

The FCA provides two important incentives for relators: a significant bounty and whistle-blower protection. A relator is entitled to 15-25% of the proceeds of the action or settlement of a claim in which the government intervenes, id. § 3730(d)(1), and as much as 25-30% if the government does not intervene. Id. § 3730(d)(2).

In crafting whistle-blower protections, Congress aimed “to make employees feel more secure in reporting fraud to the United States.” Neal v. Honeywell Inc., 33 F.3d 860, 863 (7th Cir. 1994), abrogated on other grounds by Graham County Soil & Water Conservation Dist. v. United States ex rel. Wil- son, 545 U.S. 409, 416-17 (2005). Employees who investigate and supply information concerning the fraudulent practices of an employer are protected from retaliation, whether the employee or the government brings suit against the employer. 31 U.S.C. § 3730(h); Neal, 33 F.3d at 863-65.

Nothing in the text or the legislative history of the FCA addresses the potential preclusive effect of a settlement among the government, a relator, and a qui tam defendant vis- a-vis a subsequent claim by the qui tam defendant against a third party. As one treatise notes, “[t]he legislative history of the 1986 amendments [to the False Claims Act] does not dis- cuss the availability of indemnity or contribution, but does emphasize the strong public policy of encouraging whistle- blowers to come forward.” 1 John T. Boese, Civil False Claims and Qui Tam Actions § 4.10[B] at 4-258.1 (3d ed. 2006). Congress did contemplate, however, that disputes would be resolved through settlement. See, e.g., 31 U.S.C. § 3730(d)(1), (3) (specifying the proportion of the proceeds of an “action or settlement” a relator is entitled to receive). Con- gress also specifically contemplated the potential preclusive effects those final judgments rendered in other proceedings CELL THERAPEUTICS v. LASH GROUP 15309 would have on qui tam actions. Section 3731(e) of the current version of the Act provides that

a final judgment rendered in favor of the United States in any criminal proceeding charging fraud or false statements, whether upon a verdict after trial or upon a plea of guilty or nolo contendere, shall estop the defendant from denying the essential elements of the offense in any action which involves the same transaction as in the criminal proceeding and which is brought under subsection (a) or (b) of section 3730 [of the FCA].

31 U.S.C. § 3731(e).

B. FACTUAL BACKGROUND2

Cell Therapeutics, Inc. (“CTI”) developed a cancer drug called Trisonex, which the Food and Drug Administration (“FDA”) approved in September 2000 for the treatment of a particularly virulent form of leukemia. This was the first time CTI, a small and relatively young biotechnology company, had received FDA approval, so it turned to Documedics Acquisition Co., Inc. (“Documedics”) to handle Medicare reimbursement and serve as a reimbursement consultant.

Documedics billed itself as an expert in reimbursement pro- tocol for oncology drugs, but made a serious error in advising CTI.

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