1. 87. See Okie, , supra note 43, at 440 (quoting pharmaceutical executive, “the whole purpose of large clinical trials is to fully evaluate benefits and risks … and short-changing that is not in the patients' best interest”); Society for Clinical Trials, supra note 62, at 156 (listing numerous examples, of drugs that showed initial promise, but ultimately harmful effects, evident only after placebo-controlled, randomized trials).
2. 47. Id. (“Urged on by [Penelope's] family, patient groups and politicians, including the staff of House Speaker Pelosi and Pennsylvania Gov. Edward Rendell, lobbied on behalf of giving the drug to the child.”)
3. 45. ACCESS Act, HR 6270, 110th Cong. (2008) (introduced June 12, 2008).
4. 22. 521 U.S. 702 (1997); see Abigail Alliance, 445 F.3d at 476–477 (discussing Glucksberg).
5. 44. ACCESS Act, S 3046, 110th Cong. (2008); Office of Sam Brownback, Brownback Introduces ACCESS Act, Press Release, May 21, 2008, available at (last visited March 27, 2009); FDA Law Blog, ACCESS Act Reintroduced by Sen. Brownback; Previous Tiered Approval Nomenclature Scrapped and New Immunity Provision Added, June 4, 2008, available at (last visited March 27, 2009).