scholarly journals Phase III HIV vaccine trial in Thailand: a step toward a protective vaccine for HIV

2010 ◽  
Vol 9 (9) ◽  
pp. 997-1005 ◽  
Author(s):  
Monica Vaccari ◽  
Poonam Poonam ◽  
Genoveffa Franchini
Keyword(s):  
2013 ◽  
Vol 29 (11) ◽  
pp. 1524-1534 ◽  
Author(s):  
Jaranit Kaewkungwal ◽  
Punnee Pitisuttithum ◽  
Supachai Rerks-ngarm ◽  
Sorachai Nitayaphan ◽  
Chirasak Khamboonruang ◽  
...  

2019 ◽  
Vol 4 (Suppl 3) ◽  
pp. A10.1-A10
Author(s):  
Sarah Joseph ◽  
Pontiano Kaleebu ◽  
Eugene Ruzagira ◽  
Christian Holm Hansen ◽  
Janet Seeley ◽  
...  

BackgroundThere remains an urgent need for a prophylactic HIV vaccine to control generalised epidemics. PrEP has demonstrated effectiveness of 86% and is recommended by WHO; uptake is generally high, but retention is disappointing in some settings. The EDCTP2 project PrEPVacc will assess the efficacy of two combination prophylactic vaccine regimens (DNA, MVA and Env protein/adjuvant) each compared to placebo and the proportion of infections averted by F/TAF in comparison to TDF/FTC. A Registration Cohort, recruiting HIV negative volunteers at risk of HIV will precede the trial.MethodsThe PrEPVacc partnership agreed that 70% vaccine efficacy had public health relevance. The trial uses nstage software for multi-arm, multi-stage designs (MAMS) and the averted infections ratio (AIR) methodology with participants randomised (i) 1:1:1 to active product or placebo (ii) 1:1 to TDF/FTC : F/TAF until week 26 (presumed peak immunogenicity). Access to PrEP in the Registration Cohort and after week 26 will be standard of care. HIV seroconversions occurring between weeks 0–26 will inform the PrEP analysis, incorporating HIV incidence amongst those who do not take up PrEP locally in the Registration Cohort. Seroconversions after week 26 will inform vaccine analyses.ResultsUp to 556 participants per group affords 92% power to detect vaccine efficacy of 70% at the final analysis, assuming incidence of 4/100-person years and 10% loss with 81% and 97% power to conclude that F/TAF can avert half or more of the infections prevented by TDF/FTC if effectiveness of TDF/FTC is 70% and 80%, respectively.ConclusionPrEPVacc adopts a pragmatic approach to uncertainties around HIV incidence in settings where PrEP is increasingly available. This innovative adaptive trial design uses validated software to determine vaccine efficacy and a novel methodology to evaluate a new PrEP agent, overcoming the challenge of demonstrating non-inferiority when adherence to TDF/FTC is high and the number of outcome events very low.


Retrovirology ◽  
2009 ◽  
Vol 6 (Suppl 3) ◽  
pp. O52 ◽  
Author(s):  
MS de Souza ◽  
R Trichavaroj ◽  
A Schuetz ◽  
W Chuenarom ◽  
Y Phuang-ngem ◽  
...  
Keyword(s):  

2013 ◽  
Vol 13 (1) ◽  
Author(s):  
Muhammad Bakari ◽  
Patricia Munseri ◽  
Joel Francis ◽  
Eric Aris ◽  
Candida Moshiro ◽  
...  

AIDS Care ◽  
2013 ◽  
Vol 25 (7) ◽  
pp. 910-914 ◽  
Author(s):  
Michael Evangeli ◽  
Zuhayr Kafaar ◽  
Ashraf Kagee ◽  
Leslie Swartz ◽  
Philippa Bullemor-Day

Science ◽  
2004 ◽  
Vol 303 (5660) ◽  
pp. 961-961 ◽  
Author(s):  
J. G. McNeil
Keyword(s):  

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