Publication: Executive summary and recommendations from the WHO/UNAIDS/IAVI expert group consultation on 'Phase IIB-TOC trials as a novel strategy for evaluation of preventive HIV vaccines', 31 January-2 February 2006, IAVI, New York, USA
dc.contributor.author | Jim Ackland | en_US |
dc.contributor.author | Susan Allen | en_US |
dc.contributor.author | Daniel Barth-Jones | en_US |
dc.contributor.author | Deborah Birx | en_US |
dc.contributor.author | Elwyn Chomba | en_US |
dc.contributor.author | Gavin Churchyard | en_US |
dc.contributor.author | Ann Duerr | en_US |
dc.contributor.author | Shuigao Jin | en_US |
dc.contributor.author | Margaret Johnston | en_US |
dc.contributor.author | Patricia E. Fast | en_US |
dc.contributor.author | Alan Fix | en_US |
dc.contributor.author | Mary Foulkes | en_US |
dc.contributor.author | Dean Follmann | en_US |
dc.contributor.author | Raymond Hutubessy | en_US |
dc.contributor.author | Siobhan Malone | en_US |
dc.contributor.author | Ronald Gray | en_US |
dc.contributor.author | Abhay Indrayan | en_US |
dc.contributor.author | Jonathan Levin | en_US |
dc.contributor.author | Bonnie J. Mathieson | en_US |
dc.contributor.author | Timothy D. Mastro | en_US |
dc.contributor.author | John McNeil | en_US |
dc.contributor.author | Saladin Osmanov | en_US |
dc.contributor.author | Punnee Pitisuttithum | en_US |
dc.contributor.author | Barry Peters | en_US |
dc.contributor.author | Etienne Karita | en_US |
dc.contributor.author | Michael N. Robertson | en_US |
dc.contributor.author | R. Ramakrishnan | en_US |
dc.contributor.author | Helen Rees | en_US |
dc.contributor.author | Wasima Rida | en_US |
dc.contributor.author | Yuhua Ruan | en_US |
dc.contributor.author | Eric Sandström | en_US |
dc.contributor.author | Claudia Schmidt | en_US |
dc.contributor.author | Peter Smith | en_US |
dc.contributor.author | Steven Self | en_US |
dc.contributor.author | Georges Thiry | en_US |
dc.contributor.author | Judith Wasserheit | en_US |
dc.contributor.author | Frances Priddy | en_US |
dc.contributor.author | Ibou Thior | en_US |
dc.contributor.author | Mitchell Warren | en_US |
dc.contributor.author | David Cooper | en_US |
dc.contributor.author | Pontiano Kaleebu | en_US |
dc.contributor.author | Ruth Macklin | en_US |
dc.contributor.author | Godfrey Tangwa | en_US |
dc.contributor.other | Global BioSolutions | en_US |
dc.contributor.other | Rollins School of Public Health | en_US |
dc.contributor.other | Wayne State University School of Medicine | en_US |
dc.contributor.other | Centers for Disease Control and Prevention | en_US |
dc.contributor.other | Zambia-UAB HIV Research Project | en_US |
dc.contributor.other | Ernest Oppenheimer Hospital | en_US |
dc.contributor.other | Scientific Support Unit | en_US |
dc.contributor.other | Chinese Center for Disease Control and Prevention | en_US |
dc.contributor.other | National Institute of Allergy and Infectious Diseases | en_US |
dc.contributor.other | International AIDS Vaccine Initiative | en_US |
dc.contributor.other | Food and Drug Administration | en_US |
dc.contributor.other | Organisation Mondiale de la Sante | en_US |
dc.contributor.other | Bill and Melinda Gates Foundation | en_US |
dc.contributor.other | Johns Hopkins Bloomberg School of Public Health | en_US |
dc.contributor.other | University College of Medical Sciences | en_US |
dc.contributor.other | South African Medical Research Council | en_US |
dc.contributor.other | OAR HIV/AIDS Vaccine Coordinating Committee | en_US |
dc.contributor.other | National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Guy's and St Thomas' NHS Foundation Trust | en_US |
dc.contributor.other | Projet San Francisco Rwanda | en_US |
dc.contributor.other | Merck & Co., Inc. | en_US |
dc.contributor.other | National Institute of Epidemiology | en_US |
dc.contributor.other | University of Witwatersrand | en_US |
dc.contributor.other | Statistics Collaborative | en_US |
dc.contributor.other | Karolinska University Hospital | en_US |
dc.contributor.other | London School of Hygiene & Tropical Medicine | en_US |
dc.contributor.other | Statistical Center for HIV/AIDS Research and Prevention | en_US |
dc.contributor.other | IAVI | en_US |
dc.contributor.other | HIV Vaccine Trials Network | en_US |
dc.contributor.other | Emory University | en_US |
dc.contributor.other | Botswana Harvard AIDS Institute Partnership | en_US |
dc.contributor.other | AIDS Vaccine Advocacy Coalition | en_US |
dc.contributor.other | Kirby Institute | en_US |
dc.contributor.other | Uganda Virus Research Institute | en_US |
dc.contributor.other | Albert Einstein College of Medicine of Yeshiva University | en_US |
dc.contributor.other | Universite de Yaounde I | en_US |
dc.date.accessioned | 2018-08-24T01:54:47Z | |
dc.date.available | 2018-08-24T01:54:47Z | |
dc.date.issued | 2007-02-01 | en_US |
dc.description.abstract | This report summarizes the discussions and recommendations from a consultation held in New York City, USA (31 January-2 February 2006) organized by the joint World Health Organization-United Nations Programme on HIV/AIDS HIV Vaccine Initiative and the International AIDS Vaccine Initiative. The consultation discussed issues related to the design and implementation of phase IIB 'test of concept' trials (phase IIB-TOC), also referred to as 'proof of concept' trials, in evaluating candidate HIV vaccines and their implications for future approval and licensure. The results of a single phase IIB-TOC trial would not be expected to provide sufficient evidence of safety or efficacy required for licensure. In many instances, phase IIB-TOC trials may be undertaken relatively early in development, before manufacturing processes and capacity are developed sufficiently to distribute the vaccine on a large scale. However, experts at this meeting considered the pressure that could arise, particularly in regions hardest hit by AIDS, if a phase IIB-TOC trial showed high levels of efficacy. The group largely agreed that full-scale phase III trials would still be necessary to demonstrate that the vaccine candidate was safe and effective, but emphasized that governments and organizations conducting trials should consider these issues in advance. The recommendations from this meeting should be helpful for all organizations involved in HIV vaccine trials, in particular for the national regulatory authorities in assessing the utility of phase IIB-TOC trials in the overall HIV vaccine research and development process. © 2007 Lippincott Williams & Wilkins, Inc. | en_US |
dc.identifier.citation | AIDS. Vol.21, No.4 (2007), 539-546 | en_US |
dc.identifier.doi | 10.1097/QAD.0b013e328011a0c9 | en_US |
dc.identifier.issn | 02699370 | en_US |
dc.identifier.other | 2-s2.0-33847016909 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/24593 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33847016909&origin=inward | en_US |
dc.subject | Immunology and Microbiology | en_US |
dc.subject | Medicine | en_US |
dc.title | Executive summary and recommendations from the WHO/UNAIDS/IAVI expert group consultation on 'Phase IIB-TOC trials as a novel strategy for evaluation of preventive HIV vaccines', 31 January-2 February 2006, IAVI, New York, USA | en_US |
dc.type | Review | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33847016909&origin=inward | en_US |