Asunto(s)
Ensayos de Uso Compasivo , Terapia Genética , Ensayos de Uso Compasivo/economía , Ensayos de Uso Compasivo/ética , Ensayos de Uso Compasivo/legislación & jurisprudencia , Terapia Genética/economía , Terapia Genética/ética , Terapia Genética/legislación & jurisprudencia , Humanos , Estados Unidos , United States Food and Drug AdministrationRESUMEN
OBJECTIVE: We sought to determine the characteristics of "expanded access" and "compassionate use" programs registered in ClinicalTrials.gov and to determine the percentage of drugs provided through these programs that ultimately received FDA marketing approval. RESULTS: We identified 398 expanded access and compassionate use programs (hereafter referred to as expanded access programs) registered on ClinicalTrials.gov. Industry funded 61% (n = 241) of programs individually or collaboratively, while NIH and the US Federal Government rarely funded programs (3% [n = 11] and 2% [n = 6], respectively). Most programs provided access to drugs (71% [n = 282]), 11% to biologics (n = 43), and 10% to medical devices (n = 40). These programs covered 460 unique conditions, the most common being HIV (n = 26), leukemia (22), and multiple myeloma (n = 14). Only 2% of programs reported results in ClinicalTrials.gov. Most programs (82%) were open to enrolling adults and seniors (n = 326). These programs provided access to 210 unique experimental drugs, of which 76% have received FDA approval.