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Volume 367, Issue 9518, Pages 1247-1255 (April 2006)
Sustained efficacy up to 4·5 years of a bivalent L1 virus-like particle vaccine against human papillomavirus types 16 and 18: follow-up from a randomised control trial Prof Diane M Harper, MD, Prof Eduardo L Franco, PhD, Prof Cosette M Wheeler, PhD, Prof Anna-Barbara Moscicki, MD, Barbara Romanowski, MD, Cecilia M Roteli-Martins, MD, Prof David Jenkins, MD, Anne Schuind, MD, Sue Ann Costa Clemens, MD, Gary Dubin, MD The Lancet Volume 367, Issue 9518, Pages (April 2006) DOI: /S (06) Copyright © 2006 Elsevier Ltd Terms and Conditions
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Figure 1 Trial design Follow-up time for each woman in each study phase varies dependent on when she completed her last study visit in the initial efficacy study and when she entered the extended follow-up phase. The Lancet , DOI: ( /S (06) ) Copyright © 2006 Elsevier Ltd Terms and Conditions
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Figure 2 Geometric mean titres and seropositivity rates, according to HPV type and group in according-to-protocol analyses for immunogenicity %=proportion of women seropositive. Sera from all vaccinees and a small number of samples from the placebo group of the initial study were retested. The Lancet , DOI: ( /S (06) ) Copyright © 2006 Elsevier Ltd Terms and Conditions
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