Public Citizen Health Research Group v. Food & Drug Administration

953 F. Supp. 400, 1996 U.S. Dist. LEXIS 20332, 1996 WL 784530
CourtDistrict Court, District of Columbia
DecidedOctober 17, 1996
DocketCivil Action 94-0169 RMU
StatusPublished
Cited by11 cases

This text of 953 F. Supp. 400 (Public Citizen Health Research Group v. 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
Public Citizen Health Research Group v. Food & Drug Administration, 953 F. Supp. 400, 1996 U.S. Dist. LEXIS 20332, 1996 WL 784530 (D.D.C. 1996).

Opinion

MEMORANDUM ORDER

URBINA, District Judge.

DENYING THE PARTIES’ CROSS-MOTIONS FOR SUMMARY JUDGMENT AND GRANTING DEFENDANT-INTERVENORS’ MOTION FOR A PROTECTIVE ORDER

This matter comes before the court upon the parties’ cross-motions for summary judgment. In addition, Defendant-Intervenors Anesta Corporation and Abbott Laboratories (Defendant-Intervenors) have filed a motion seeking a protective order which would forbid the disclosure by Public Citizen Health Research Group (HRG) of a table of information released to HRG by the FDA. The table was inadvertently released to HRG pursuant to a Freedom of Information Act (FOIA) request and is one of seven tables at issue in this case.

The parties’ cross-motions for summary judgment shall be denied as there are substantial issues of material fact in dispute. See Fed.R.Civ.P. 56(c). Defendant-Intervenors’ motion for a protective order shall be granted. Accordingly, HRG will not disclose or make use of the information contained in Table l.dose Variables. In addition, the portions of the court record which contain a reference to Table l.dose Variables will be sealed pending this court’s adjudication of the underlying merits of this dispute.

I. BACKGROUND

This case has its genus in a FOIA request filed with the FDA by HRG dated January 5, 1994. In its request, HRG sought all documents distributed by the FDA to its advisory committees in preparation for the August 24, 1993 advisory committee discussion on Fentanyl Oralet (Oralet). Oralet is a lollipop containing the narcotic fentanyl that was eventually approved by the FDA in October 1993. Oralet is a premedication for children who are about to undergo anesthesia and/or surgery. After receiving no response to its FOIA request, HRG filed this action on February 1,1994. In the complaint, HRG asked the court to find that the withholding of the requested information is in violation of FOIA and, further, to order the FDA to release the information to HRG. HRG seeks this information because it is concerned about the safety of Oralet and the possible negative consequences of “off-label” use by medical practitioners.

By letter dated March 9, 1994, the EDA notified HRG it had located seventy documents responsive to its request. The FDA released forty-two documents in total and fourteen documents with redacted portions. The remaining fourteen documents were withheld in their entirety. The FDA relied on exemptions four and six of FOIA in withholding this information. 1 After correspond *402 ing and reviewing the withheld documents, all parties have agreed that the only documents at issue in this matter are seven tables which contain data associated with clinical studies of Oralet performed by Defendants Intervenors and submitted to the FDA pursuant to Oralet’s New Drug Application (NDA). This data pertains to patient dosages, consumption times, drug blood concentrations, ages, heights, and weights. Exemption four of FOIA is the exemption relied upon by the FDA with regards to the nondisclosure of these tables. Included in the released documents was one of the tables entitled “Table l.dose Variables” (Table 1). The FDA claims that the release of this table was an error on its part as this document should have been withheld pursuant to exemption four of FOIA and 21 C.F.R. Section 20.61.

HRG first included Table 1 in Plaintiffs Opposition to Defendant’s and DefendantIntervenors’ Motion for a Protective Order, dated April 18, 1994 Defendant-Intervenors first mentioned the allegedly illegitimate release of Table 1 in their Motions for Summary Judgment filed on May 25,1994. HRG inserted Table 1 in another pleading dated August 19, 1994, Plaintiffs Reply to Defendant’s and Defendant-Intervenors’ Opposition to Plaintiffs Cross-Motion for Summary Judgment. Defendant-Intervenors filed this motion for a protective order some three months after they apparently first learned of Table l’s release.

II. DISCUSSION

A. Summary Judgment

When more than one party moves for summary judgment, each -party must carry its own burden of proof. United States Dep’t. of Justice v. Reporter’s Comm. for Freedom of the Press, 489 U.S. 749, 755, 109 S.Ct. 1468, 1472-73, 103 L.Ed.2d 774 (1989). In order to meet its burden, the moving party must prove that no genuine issue of material fact is in dispute and that it is entitled to judgment as a matter of law. Fed.R.Civ.P. 56(c); National Cable Television Assoc., Inc. v. Federal Communications Commission, 479 F.2d 183, 186 (D.C.Cir.1973).

In FOIA cases, a court “may grant summary judgment solely on the basis of agency affidavits if they are clear, specific and reasonably detailed, and there is no contradictory evidence on the reeord[.]” Hayden v. National Sec. Agency/Cent. Sec. Serv., 608 F.2d 1381, 1387 (D.C.Cir.1979), cert. denied, 446 U.S. 937, 100 S.Ct. 2156, 64 L.Ed.2d 790 (1980). However, since summary judgment is such a “drastic remedy, courts should grant it with caution so that no person will be deprived of his or her day in court to prove a disputed material factual issue.” Greenberg v. FDA 803 F.2d 1213, 1216 (D.C.Cir.1986).

The central issue in this case is whether the information sought by HRG is exempt from disclosure pursuant to exemption four of FOIA because the public dissemination of this information would cause substantial harm to the competitive positions of Defendant-Intervenors. All of the parties have submitted affidavits supporting their respective positions on this issue. Expectedly, the -experts for HRG declare that the dissemination of this information will in no way harm the competitive, positions of Defendant-Intervenors. Conversely, the experts offered by Defendant FDA and Defendant Intervenors posit that making this information public will cause substantial harm to the competitive positions of both Anesta and Abbott.

In circumstances such as the ones presented in this case, the D.C. Circuit Court of Appeals has cautioned against the resolution of the dispute via summary judgment. In Greenberg v. FDA 803 F.2d 1213 (D.C.Cir.1986), a FOIA “exemption four” case similar to the case presently before the court, a staff attorney with HRG requested from the FDA a list of customers who had purchased CAT scanners from a manufacturer. Id. at 1214. The FDA refused to release the information; and Mr. Greenberg sued. Id.

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Cite This Page — Counsel Stack

Bluebook (online)
953 F. Supp. 400, 1996 U.S. Dist. LEXIS 20332, 1996 WL 784530, Counsel Stack Legal Research, https://law.counselstack.com/opinion/public-citizen-health-research-group-v-food-drug-administration-dcd-1996.