Reply to Commentary Are HIV-Infected Candidates for Participation in Risky Cure-Related Studies Otherwise Healthy?
We respond to Eyal et al.’s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background sta...
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Published in | Journal of empirical research on human research ethics Vol. 13; no. 1; pp. 23 - 25 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Los Angeles, CA
Sage Publications, Ltd
01.02.2018
SAGE Publications Sage Publications Ltd |
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Online Access | Get full text |
ISSN | 1556-2646 1556-2654 1556-2654 |
DOI | 10.1177/1556264617741715 |
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Abstract | We respond to Eyal et al.’s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background standard of care. As the field of HIV cure research advances, more nuance and granularity will be needed to define research criteria and acceptable risk/benefit ratios for cure study participants, as well as specific tiered protocol designs that serve to protect various participant populations from untoward risks, especially in very early phase research with interventions known to have potentially serious toxicities. We highlight key lessons from the ACTIVATE study involving a latency-reversing agent, Panobinostat, for HIV cure study design involving “otherwise healthy volunteers”. |
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AbstractList | We respond to Eyal et al.’s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background standard of care. As the field of HIV cure research advances, more nuance and granularity will be needed to define research criteria and acceptable risk/benefit ratios for cure study participants, as well as specific tiered protocol designs that serve to protect various participant populations from untoward risks, especially in very early phase research with interventions known to have potentially serious toxicities. We highlight key lessons from the ACTIVATE study involving a latency-reversing agent, Panobinostat, for HIV cure study design involving “otherwise healthy volunteers”. We respond to Eyal et al.'s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background standard of care. As the field of HIV cure research advances, more nuance and granularity will be needed to define research criteria and acceptable risk/benefit ratios for cure study participants, as well as specific tiered protocol designs that serve to protect various participant populations from untoward risks, especially in very early phase research with interventions known to have potentially serious toxicities. We highlight key lessons from the ACTIVATE study involving a latency-reversing agent, Panobinostat, for HIV cure study design involving "otherwise healthy volunteers".We respond to Eyal et al.'s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of participants enrolled in research cannot be dissociated from the study interventions, the types of anticipated risks, and the background standard of care. As the field of HIV cure research advances, more nuance and granularity will be needed to define research criteria and acceptable risk/benefit ratios for cure study participants, as well as specific tiered protocol designs that serve to protect various participant populations from untoward risks, especially in very early phase research with interventions known to have potentially serious toxicities. We highlight key lessons from the ACTIVATE study involving a latency-reversing agent, Panobinostat, for HIV cure study design involving "otherwise healthy volunteers". |
Author | Sylla, Laurie Dubé, Karine Dee, Lynda |
Author_xml | – sequence: 1 givenname: Karine surname: Dubé fullname: Dubé, Karine organization: Public Health Leadership Program (PHLP), University of North Carolina Gillings School of Global Public Health, Chapel Hill, NC, USA – sequence: 2 givenname: Laurie surname: Sylla fullname: Sylla, Laurie organization: defeatHIV Community Advisory Board (CAB), Seattle, CA, USA – sequence: 3 givenname: Lynda surname: Dee fullname: Dee, Lynda organization: amfAR Institute for HIV Cure Research CAB, San Francisco, CA, USA |
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Cites_doi | 10.3390/v5112898 10.1097/QAD.0000000000001300 10.1136/medethics-2015-103113 10.1097/QAD.0000000000001109.Inflammation |
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References | Nou, Lo, Grinspoon 2016; 30 DiGiusto, Stan, Krishnan, Li, Rossi, Zaia 2013; 5 Kuritzkes 2016; 43 Gianella, Taylor, Brown, Kaytes, Achim, Moore, Smith 2017; 31 bibr2-1556264617741715 bibr1-1556264617741715 bibr3-1556264617741715 bibr5-1556264617741715 bibr4-1556264617741715 29179624 - J Empir Res Hum Res Ethics. 2018 Feb;13(1):18-22 28984168 - J Empir Res Hum Res Ethics. 2018 Feb;13(1):3-17 |
References_xml | – volume: 43 start-page: 67 year: 2016 end-page: 70 article-title: Why cure, why now? publication-title: Journal of Medical Ethics – volume: 30 start-page: 1495 year: 2016 end-page: 1509 article-title: Inflammation, immune activation, and cardiovascular disease in HIV publication-title: AIDS – volume: 5 start-page: 2898 year: 2013 end-page: 2919 article-title: Development of hematopoietic stem cell based gene therapy for HIV-1 infection: Considerations for proof of concept studies and translation to standard medical practice publication-title: Viruses – volume: 31 start-page: 1 issue: 1 year: 2017 end-page: 4 article-title: Can research at the end of life be a useful tool to advance HIV cure? publication-title: AIDS – ident: bibr2-1556264617741715 – ident: bibr1-1556264617741715 doi: 10.3390/v5112898 – ident: bibr3-1556264617741715 doi: 10.1097/QAD.0000000000001300 – ident: bibr4-1556264617741715 doi: 10.1136/medethics-2015-103113 – ident: bibr5-1556264617741715 doi: 10.1097/QAD.0000000000001109.Inflammation – reference: 29179624 - J Empir Res Hum Res Ethics. 2018 Feb;13(1):18-22 – reference: 28984168 - J Empir Res Hum Res Ethics. 2018 Feb;13(1):3-17 |
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Snippet | We respond to Eyal et al.’s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of... We respond to Eyal et al.'s commentary focusing on how people living with HIV participating in HIV cure-related studies are defined. We argue that the types of... |
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SubjectTerms | Clinical trials Ethical Issues in Clinical Trials Health HIV Human immunodeficiency virus Human subjects Participation |
Subtitle | Are HIV-Infected Candidates for Participation in Risky Cure-Related Studies Otherwise Healthy? |
Title | Reply to Commentary |
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