21 U.S.C. § 360dd — Open protocols for investigations of drugs for rare diseases or conditions
submitted 88 years ago by Pub. L. 97-414 to r/title-21-FOOD-AND-DRUGS · 101 words · no verdicts yet
If a drug is designated for a rare disease and has an investigational exemption on file, the FDA must encourage its sponsor to design open study protocols. These protocols should let patients who need the drug, and can't use other treatments, join the trials.
If a drug* is designated under section 360bb of this title as a drug for a rare disease or condition and if notice of a claimed exemption under section 355(i) of this title or regulations issued thereunder is filed for such drug, the Secretary* shall encourage the sponsor of such drug to design protocols for clinical investigations of the drug which may be conducted under the exemption to permit the addition to the investigations of persons with the disease or condition who need the drug to treat the disease or condition and who cannot be satisfactorily treated by available alternative drugs.
Source credit: (June 25, 1938, ch. 675, § 528, as added Pub. L. 97–414, § 2(a), Jan. 4, 1983, 96 Stat. 2051.)
- 1938Enacted · Pub. L. 97-414 · 96 Stat. 2051
A history note hasn’t been published yet. The record shows enactment by Pub. L. 97-414 on 1938-06-25.
all 0 arguments · sorted by: best
no arguments yet — make the first case