Right to Experimental Treatment: FDA New Drug Approval, Constitutional Rights, and the Public's Health

Author:

Leonard Elizabeth Weeks

Abstract

Do terminally ill patients who have exhausted all other available, government-approved treatment options have a constitutional right to experimental treatment that may prolong their lives? On May 2, 2006, a divided panel of the U.S. Court of Appeals for the District of Columbia, in a startling opinion, Abigail Alliance for Better Access to Developmental Drugs v. Von Eschenbach, held “Yes.” The plaintiffs, Abigail Alliance for Better Access to Developmental Drugs (Abigail Alliance) and Washington Legal Foundation, sought to enjoin the Food and Drug Administration (FDA) from refusing to allow the sale of investigational new drugs that had not yet received FDA approval. The terminally ill plaintiffs contended that they quite literally could not wait that long for the drugs. With no other treatment options available, the plaintiffs urged the court to recognize a fundamental, constitutional right to take potentially life-saving or life-prolonging drugs, even though the treatment had not been fully tested through human trials for safety and effectiveness and could not be legally marketed to the public.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference103 articles.

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).

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