AHF Sues FDA Over Information on Gilead Sciences, Inc.'s HIV Prevention Pill

WASHINGTON--(BUSINESS WIRE)--AIDS Healthcare Foundation (AHF) today filed a lawsuit against the Food and Drug Administration (FDA) over its denial of AHF’s Freedom of Information Act (FOIA) requests regarding correspondence between the FDA and Gilead Sciences regarding its potential application to the FDA to expand the use of its AIDS drug, Truvada, for use as an HIV prevention pill for pre-exposure prophylaxis (PrEP) in uninfected individuals. The legal action was filed in the United States District Court, Central District of California. According to AHF’s suit, the action is being, “…brought under the Freedom of Information Act, 5 U.S.C. Section 552, as amended, to enjoin defendants from withholding from public disclosure certain records of the United States Food and Drug Administration (“FDA”),” and seeks, “To enjoin the FDA from withholding FDA records,” and “To order the production of any FDA records improperly withheld from AHF.”
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