Campaign for Responsible Transplantation v. United States Food & Drug Administration

448 F. Supp. 2d 146, 2006 U.S. Dist. LEXIS 62615, 2006 WL 2536466
CourtDistrict Court, District of Columbia
DecidedSeptember 5, 2006
DocketCivil Action No.: 00-2849 (RMU)
StatusPublished
Cited by3 cases

This text of 448 F. Supp. 2d 146 (Campaign for Responsible Transplantation v. United States Food & Drug Administration) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Campaign for Responsible Transplantation v. United States Food & Drug Administration, 448 F. Supp. 2d 146, 2006 U.S. Dist. LEXIS 62615, 2006 WL 2536466 (D.D.C. 2006).

Opinion

MEMORANDUM OPINION

RICARDO M. URBINA, District Judge.

Denying the Plaintiff’s Motion for an Award of Attorney’s Fees and Costs

I. INTRODUCTION

The plaintiff, Campaign for Responsible Transplantation (“CRT”), is a non-profit organization dedicated to increasing awareness of the dangers of a cellular treatment therapy called xenotransplantation. CRT brought suit to compel defendant Food and Drug Administration (“FDA”), to disclose documents related to clinical trials involving xenotransplantation. During the course of the litigation, the defendant voluntarily released some documents and the court ruled that the defendant was justified in withholding the documents it did not release. The plaintiff now moves for attorney’s fees pursuant to the Freedom of Information Act (“FOIA”), 5 U:S.C. § 552(a)(4)(E)(a). The court denies the plaintiffs motion for attorney’s fees because the plaintiff did not substantially prevail on the merits of its claims.

II. BACKGROUND

Xenotransplantation (“XTP”) involves the implantátion of animal tissues, cells and organs into human beings for treatment of human diseases. Mem. Op. (Jul. 23, 2001) at 1. The FDA regulates XTP *148 products as “investigational new drugs” (“INDs”). Id. at 2. The plaintiff, concerned about potential public health risks of XTP products, submitted a written FOIA request for records related to thirty-five XTP INDs on March 9, 2000. Mem. Op. (Sept. 3, 2002) at 3. The FDA acknowledged receipt of the request and indicated it would respond to the request “as soon as possible.” Id. When the plaintiff did not receive a response to its FOIA request by August 2, 2000, the plaintiff filed an appeal with the FDA. Id. After the defendant failed to respond to the plaintiffs appeal, it filed suit in this court on November 27, 2000 to compel immediate disclosure of the requested records. Id. After commencing suit, the plaintiff narrowed its original FOIA request to include only documents generated by the defendant and documents concerning clinical trials related to nineteen of the thirty-five INDs. Mem. Op. (Sept. 24, 2004) at 3.

The plaintiff, in an effort to further narrow the scope of the litigation, moved for Vaughn indices 2 describing documents related to all nineteen INDs. Mem. Op. (July 23, 2001) at 3-4. The defendant countered that such a request would take an estimated two years to complete because it involved review of about 240,000 pages of documents. Id. at 6. In its cross-motion, the defendant asked the court to instead allow it to produce a sample index with respect to one of the nineteen INDs. Id. at 6-7. The defendant supported its motion by noting that the “same types of FDA-generated documents are found in every xenotransplantation IND file, and that they would assert the same exemptions for documents in the indexed IND as it would for the same types of documents in the other INDs.” Id. at 8. The court’s 2001 opinion denied the plaintiffs motion for Vaughn indices for all INDs, and instead granted the FDA’s motion to produce a sample Vaughn index for one IND (“IND G”). Id. at 7. The FDA produced a sample Vaughn index for IND G on September 4, 2001. Pl.’s Mot. for Summ. J. (Jan. 15, 2002) at 22. The court later used the sample index as the basis for a ruling covering all of the INDs subject to the plaintiffs FOIA request. Pl.’s Mot. to Enforce Sept. 24, 2004 Order. On October 15, 2001, the FDA also released responsive documents that it did not plan to exempt from disclosure. Pl.’s Mot. for Summ. J. (Jan. 15, 2002) at 23.

After the FDA produced the sample index and released some documents related to the sample IND, both parties moved for summary judgment over the IND G documents that the FDA continued to withhold. Mem. Op. (Sept. 24, 2004) at 3. The plaintiff moved for the immediate release of all IND G documents that the FDA claimed were exempt. Pl.’s Mot. for Summ. J. (Jan. 15, 2002). The defendant, conversely, moved the court for a ruling that the withheld documents were exempt from disclosure. Def.’s Mot. for Summ. J. (Mar. 29, 2002). On September 3, 2002, the court granted in part and denied in part both summary judgment motions, concluding that the FDA conducted an adequate search, but that its sample Vaughn index was inadequate to justify the withholdings.' Mem. Op. (Sept. 3, 2002) at 16. Rather than rule on the propriety of the defendant’s decision to withhold documents by relying on an inadequate Vaughn index, the court postponed judgment on the mer *149 its of the parties’ claims and ordered the FDA produce a revised sample Vaughn index. Id.

While preparing its revised Vaughn index for IND G, the FDA released additional documents that it did not plan to withhold. After the FDA produced its revised sample Vaughn index, the parties filed renewed cross-motions for summary judgment. Mem. Op. (Sept. 24, 2004) at 3. On September 24, 2004, the court denied the plaintiffs motion for immediate release of withheld documents and instead granted the defendant’s motion, holding that the FDA lawfully withheld contested documents pursuant to FOIA exemptions. Id. at 23. Because the Vaughn index and the court’s ruling related only to the sample IND G, the court also ordered the FDA to release all non-exempt documents related to the other eighteen INDs. Id. at 22. Months later, after the defendant had not released the documents with respect to the other eighteen INDs, the plaintiff moved to enforce the court’s order. The court denied the plaintiffs request, stating that “[t]he parties’ submissions demonstrate that they have not adequately communicated with each other ... [and] the court is confident that the parties do not wish to further burden the court with the task of unraveling unnecessary disputes.” Order (June 3, 2005). The court now turns to the plaintiffs motion for attorney fees and costs.

III. ANALYSIS

A. Legal Standard for Awarding Attorney’s Fees in the FOIA Context

Pursuant to 5 U.S.C. § 552(a)(4)(E)(a), the court may assess “reasonable attorney fees and other litigation costs reasonably incurred in any case ... in which the complainant has substantially prevailed.” 3 To award attorney’s fees under FOIA, a court must undertake a two-step inquiry. First, the court must determine whether the claimant is eligible for attorney’s fees. Pyramid Lake Paiute Tribe v. U.S. Dep’t of Justice, 750 F.2d 117, 119 (D.C.Cir.1984). To be eligible for fees, the claimant must “substantially prevail” in the underlying FOIA litigation. Id. Second, the court must determine that the plaintiff is “entitled” to an award of attorney’s fees and costs. Md. Dep’t of Human Res.

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Bluebook (online)
448 F. Supp. 2d 146, 2006 U.S. Dist. LEXIS 62615, 2006 WL 2536466, Counsel Stack Legal Research, https://law.counselstack.com/opinion/campaign-for-responsible-transplantation-v-united-states-food-drug-dcd-2006.