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All Federal Register documents (rules, proposed rules, notices, presidential documents) from 1994 to present.

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2015-02561 Individual Patient Expanded Access Applications: Form FDA 3926; Draft Guidance for Industry; Availability Rule The Food and Drug Administration (FDA or the Agency) is announcing the availability of a draft guidance for industry entitled "Individual Patient Expanded Access Applications: Form FDA 3926." The draft guidance provides for public comment and describes draft Form FDA 3926 (Individual Patient Expanded Access--Investigational New Drug Application (IND)), which, when finalized, FDA intends to make available for licensed physicians to use for expanded access requests for individual patient INDs. Individual patient expanded access allows for the use of an investigational drug outside of a clinical trial for an individual patient who has a serious or immediately life-threatening disease or condition and there is no comparable or satisfactory alternative therapy to diagnose, monitor, or treat the disease or condition. When finalized, draft Form FDA 3926 is intended to provide a streamlined alternative for submitting an Investigational New Drug Application (IND) for use in cases of individual patient expanded access. 2015-02-10 2015 2 https://www.federalregister.gov/documents/2015/02/10/2015-02561/individual-patient-expanded-access-applications-form-fda-3926-draft-guidance-for-industry https://www.govinfo.gov/content/pkg/FR-2015-02-10/pdf/2015-02561.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA or the Agency) is announcing the availability of a draft guidance for industry entitled "Individual Patient Expanded Access Applications: Form FDA 3926." The draft guidance provides for public comment and describes...

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