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dc.creatorTaylor, Douglas.
dc.creatorGrobler, Anna Christina.
dc.creatorAbdool Karim, Salim Safurdeen.
dc.date.accessioned2013-06-27T13:41:46Z
dc.date.available2013-06-27T13:41:46Z
dc.date.created2012
dc.date.issued2012
dc.identifier.citationTaylor, D.J., Grobler, A., Abdool Karim, S.S. 2012. An adaptive design to bridge the gap between phase 2b/3 microbicide effectiveness trials and evidence required for licensure. Clin Trials 9 (4) pp. 377-384.en
dc.identifier.issn1740-7745
dc.identifier.urihttp://dx.doi.org/10.1177/1740774512445512en
dc.identifier.urihttp://hdl.handle.net/10413/9217
dc.description.abstractBackground. Vaginally and rectally applied microbicides are being developed to help prevent sexual acquisition of HIV. Due to the lack of surrogate outcomes, the path toward licensure typically moves directly from expanded safety studies to expensive Phase 2b/3 trials with rare incident infection outcomes. The need to confirm an initial trial’s significant finding can lead to serious delays in implementing essential programs to reduce the spread of HIV. Purpose. To propose an adaptive design where a Phase 2b/3 study powered to detect a clinically meaningful effect with evidence of one trial (observing one-sided p < 0.025) is allowed to expand by a prespecified, feasible amount if interim data suggest the chance of further achieving a more robust evidence threshold ( p < 0.001, potentially sufficient for licensure from a single trial) is promising. Methods. As an example, prespecified conditional power criteria are used to determine whether a 90-event trial with 90% power to detect a 50% reduction in risk should be expanded to 130 events. Asymptotic results and simulations are used to assess false-positive error rates and other operating characteristics of the design. Results. False-positive error rates can be controlled at the desired 0.025 and 0.001 levels with appropriate choice of critical values or expansion criteria. The chance of achieving robust evidence can approach that of a 130-event trial with traditional stopping boundaries (controlling a = 0.001) but with substantially lower expected size for plausible effectiveness levels. Limitations. Conditional power calculations assume the interim estimate of effect is an unbiased estimate for the remainder of the trial, an assumption which may not hold if product adherence varies over time. Observing a measure of effect with p < 0.001 may not be sufficient for licensure. A decision to expand the trial would be informative to investigators regarding the interim effect size. Conclusions. A moderate increase in trial size can make the difference between a study with good power to detect a clinically meaningful effect and one which may reasonably obtain the robust evidence required for regulatory bodies and public health programs to consider making a new microbicide available to persons at risk of HIV infection. The proposed design allows for this possibility while not requiring investigators to make an up-front commitment to a prohibitively large trial.en
dc.language.isoenen
dc.publisherSage.en
dc.subjectClinical trials--Methodology.en
dc.subjectHIV infections--Prevention.en
dc.subjectAntiretroviral agents.en
dc.subjectSexually transmitted diseases--Drug therapy.en
dc.subject.otherMicrobicides.en
dc.subject.otherHIV/AIDS clinical trials.en
dc.titleAn adaptive design to bridge the gap between phase 2b/3 microbicide effectiveness trials and evidence required for licensure.en
dc.typePeer reviewed journal articleen


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