Inclusion of key populations in clinical trials of new antituberculosis treatments : current barriers and recommendations for pregnant and lactating women, children, and HIV-infected persons

dc.contributor.authorGupta, Amitaen_ZA
dc.contributor.authorHughes, Michael D.en_ZA
dc.contributor.authorGarcia-Prats, Anthony J.en_ZA
dc.contributor.authorMcIntire, Katherineen_ZA
dc.contributor.authorHesseling, Anneke C.en_ZA
dc.date.accessioned2021-09-29T06:49:06Z
dc.date.available2021-09-29T06:49:06Z
dc.date.issued2019
dc.descriptionCITATION: Gupta, A., et al. 2019. Inclusion of key populations in clinical trials of new antituberculosis treatments : current barriers and recommendations for pregnant and lactating women, children, and HIV-infected persons. PLoS Medicine, 16(8):e1002882, doi:10.1371/journal.pmed.1002882.
dc.descriptionThe original publication is available at https://journals.plos.org/plosmedicine
dc.description.abstractENGLISH ABSTRACT: Pregnant women, children < 15 years old and, HIV-infected persons contribute approximately 20% of the global tuberculosis (TB) burden, with an estimated 216,000, 1,000,000, and 1,040,000 cases each year, respectively, yet these populations are currently largely excluded from TB clinical trials, leading to suboptimal treatment and poor access to new therapeutics. • Special considerations in these populations include specific TB disease spectrum and severity, lower sensitivity of commonly used TB diagnostic tests, potential differential drug dosing and treatment responses, drug–drug interactions, and challenges in acquiring high-quality data through clinical trials. • To counter the automatic exclusion of pregnant and lactating women that currently pervades the TB trial landscape, early discussions among trialists, pharmaceutical companies, maternal–child clinical experts, ethicists, and regulatory bodies are needed to address risks, benefits, and compelling rationale for inclusion. Reconsenting women when pregnancy occurs on a trial to allow continuation of study drug by informed choice is a practical and valuable approach to expand the currently limited evidence base. • Children tend to have less severe, often paucibacillary TB disease and may respond better to treatment than adults. Consequently, trials of shorter, less intense TB treatment regimens in children are needed; pharmacokinetic and safety studies should be initiated earlier and involve age groups in parallel rather than in an age-de-escalation approach. More rapid development of child-friendly drug formulations is needed. • All HIV-infected populations, including those with advanced disease, who are likely to be the intended population of the TB therapy, should be involved in Phase IIb and/or Phase III trials, as appropriate, to maximize knowledge of treatment, toxicities, drug– drug interactions, and outcomes.en_ZA
dc.description.versionPublisher's version
dc.format.extent26 pagesen_ZA
dc.identifier.citationGupta, A., et al. 2019. Inclusion of key populations in clinical trials of new antituberculosis treatments : current barriers and recommendations for pregnant and lactating women, children, and HIV-infected persons. PLoS Medicine, 16(8):e1002882, doi:10.1371/journal.pmed.1002882
dc.identifier.issn1549-1676 (online)
dc.identifier.issn1549-1277 (print)
dc.identifier.otherdoi:10.1371/journal.pmed.1002882
dc.identifier.urihttp://hdl.handle.net/10019.1/123095
dc.language.isoen_ZAen_ZA
dc.publisherPublic Library of Scienceen_ZA
dc.rights.holderAuthors retain copyrighten_ZA
dc.subjectAntitubercular agentsen_ZA
dc.subjectClinical trials of drugsen_ZA
dc.subjectLactationen_ZA
dc.subjectHIV-positive personsen_ZA
dc.subjectAntibacterial agents -- Childrenen_ZA
dc.titleInclusion of key populations in clinical trials of new antituberculosis treatments : current barriers and recommendations for pregnant and lactating women, children, and HIV-infected personsen_ZA
dc.typeArticleen_ZA
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