| Literature DB >> 28507222 |
Michelle Hume1, Linda L Lewis2, Robert M Nelson3.
Abstract
The ability of adolescents to access safe and effective new products for HIV prevention and treatment is optimised by adolescent licensure at the same time these products are approved and marketed for adults. Many adolescent product development programmes for HIV prevention or treatment products may proceed simultaneously with adult phase III development programmes. Appropriately implemented, this strategy is not expected to delay licensure as information regarding product efficacy can often be extrapolated from adults to adolescents, and pharmacokinetic properties of drugs in adolescents are expected to be similar to those in adults. Finally, adolescents enrolled in therapeutic HIV prevention and treatment research can be considered adults, based on US Food and Drug Administration (FDA) regulations and the appropriate application of state law. The FDA permits local jurisdictions to apply state and local HIV/sexually transmitted infection minor treatment laws so that adolescents who are HIV-positive or at risk of contracting HIV may be enrolled in therapeutic or prevention trials without obtaining parental permission. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.Entities:
Keywords: Children; Clinical trials; HIV Infection and AIDS; Minors/Parental Consent; Research Ethics
Mesh:
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Year: 2017 PMID: 28507222 PMCID: PMC5685924 DOI: 10.1136/medethics-2016-103600
Source DB: PubMed Journal: J Med Ethics ISSN: 0306-6800 Impact factor: 2.903