Long-term safety and efficacy of emtricitabine and tenofovir alafenamide vs emtricitabine and tenofovir disoproxil fumarate for HIV-1 pre-exposure prophylaxis: week 96 results from a randomised, double-blind, placebo-controlled, phase 3 trial

In DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil fumarate showed non-inferior efficacy for HIV prevention and improved bone mineral density and renal safety biomarkers at week 48. We report outcome...

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Vydáno v:The lancet HIV Ročník 8; číslo 7; s. e397
Hlavní autoři: Ogbuagu, Onyema, Ruane, Peter J, Podzamczer, Daniel, Salazar, Laura C, Henry, Keith, Asmuth, David M, Wohl, David, Gilson, Richard, Shao, Yongwu, Ebrahimi, Ramin, Cox, Stephanie, Kintu, Alexander, Carter, Christoph, Das, Moupali, Baeten, Jared M, Brainard, Diana M, Whitlock, Gary, Brunetta, Jason M, Kronborg, Gitte, Spinner, Christoph D
Médium: Journal Article
Jazyk:angličtina
Vydáno: Netherlands 01.07.2021
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ISSN:2352-3018, 2352-3018
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Abstract In DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil fumarate showed non-inferior efficacy for HIV prevention and improved bone mineral density and renal safety biomarkers at week 48. We report outcomes analysed after all participants had completed 96 weeks of follow-up. This study is an ongoing, randomised, double-blind, multicentre, active-controlled, phase 3, non-inferiority trial done at 94 community, public health, and hospital-associated clinics located in Europe and North America. Adult cisgender men and transgender women who have sex with men, both with a high risk of acquiring HIV as determined by self-reported sexual behaviour or recent sexually transmitted infections, were randomly assigned (1:1) to receive either emtricitabine and tenofovir alafenamide (200/25 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir alafenamide group), or emtricitabine and tenofovir disoproxil fumarate (200/300 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir disoproxil fumarate group). The primary efficacy outcome was incident HIV infection. Incidence of HIV-1 infection per 100 person-years was assessed when the last participant had completed 96 weeks of follow-up. This trial is registered with ClinicalTrials.gov, number NCT02842086. Between Sept 13, 2016, and June 30, 2017, 5387 participants were randomly assigned to receive emtricitabine and tenofovir alafenamide (n=2694) or emtricitabine and tenofovir disoproxil fumarate (n=2693), contributing 10 081 person-years of follow-up. At 96 weeks of follow-up, there were eight HIV infections in participants who had received emtricitabine and tenofovir alafenamide (0·16 infections per 100 person-years [95% CI 0·07-0·31]) and 15 in participants who had received emtricitabine and tenofovir disoproxil fumarate (0·30 infections per 100 person-years [0·17-0·49]). Emtricitabine and tenofovir alafenamide maintained its non-inferiority to emtricitabine and tenofovir disoproxil fumarate for HIV prevention (IRR 0·54 [95% CI 0·23-1·26]). Approximately 78-82% of participants reported taking study medication more than 95% of the time across all study visits. Rates of sexually transmitted infections remained high and similar across groups (21 cases per 100 person-years for rectal gonorrhoea and 28 cases per 100 person-years for rectal chlamydia). Emtricitabine and tenofovir alafenamide continued to show superiority over emtricitabine and tenofovir disoproxil fumarate in all but one of the six prespecified bone mineral density and renal biomarkers. There was more weight gain among participants who had received emtricitabine and tenofovir alafenamide (median weight gain 1·7 kg vs 0·5 kg, p<0·0001). Emtricitabine and tenofovir alafenamide is safe and effective for longer-term pre-exposure prophylaxis in cisgender men and transgender women who have sex with men. Gilead Sciences.
AbstractList In DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil fumarate showed non-inferior efficacy for HIV prevention and improved bone mineral density and renal safety biomarkers at week 48. We report outcomes analysed after all participants had completed 96 weeks of follow-up.BACKGROUNDIn DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil fumarate showed non-inferior efficacy for HIV prevention and improved bone mineral density and renal safety biomarkers at week 48. We report outcomes analysed after all participants had completed 96 weeks of follow-up.This study is an ongoing, randomised, double-blind, multicentre, active-controlled, phase 3, non-inferiority trial done at 94 community, public health, and hospital-associated clinics located in Europe and North America. Adult cisgender men and transgender women who have sex with men, both with a high risk of acquiring HIV as determined by self-reported sexual behaviour or recent sexually transmitted infections, were randomly assigned (1:1) to receive either emtricitabine and tenofovir alafenamide (200/25 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir alafenamide group), or emtricitabine and tenofovir disoproxil fumarate (200/300 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir disoproxil fumarate group). The primary efficacy outcome was incident HIV infection. Incidence of HIV-1 infection per 100 person-years was assessed when the last participant had completed 96 weeks of follow-up. This trial is registered with ClinicalTrials.gov, number NCT02842086.METHODSThis study is an ongoing, randomised, double-blind, multicentre, active-controlled, phase 3, non-inferiority trial done at 94 community, public health, and hospital-associated clinics located in Europe and North America. Adult cisgender men and transgender women who have sex with men, both with a high risk of acquiring HIV as determined by self-reported sexual behaviour or recent sexually transmitted infections, were randomly assigned (1:1) to receive either emtricitabine and tenofovir alafenamide (200/25 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir alafenamide group), or emtricitabine and tenofovir disoproxil fumarate (200/300 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir disoproxil fumarate group). The primary efficacy outcome was incident HIV infection. Incidence of HIV-1 infection per 100 person-years was assessed when the last participant had completed 96 weeks of follow-up. This trial is registered with ClinicalTrials.gov, number NCT02842086.Between Sept 13, 2016, and June 30, 2017, 5387 participants were randomly assigned to receive emtricitabine and tenofovir alafenamide (n=2694) or emtricitabine and tenofovir disoproxil fumarate (n=2693), contributing 10 081 person-years of follow-up. At 96 weeks of follow-up, there were eight HIV infections in participants who had received emtricitabine and tenofovir alafenamide (0·16 infections per 100 person-years [95% CI 0·07-0·31]) and 15 in participants who had received emtricitabine and tenofovir disoproxil fumarate (0·30 infections per 100 person-years [0·17-0·49]). Emtricitabine and tenofovir alafenamide maintained its non-inferiority to emtricitabine and tenofovir disoproxil fumarate for HIV prevention (IRR 0·54 [95% CI 0·23-1·26]). Approximately 78-82% of participants reported taking study medication more than 95% of the time across all study visits. Rates of sexually transmitted infections remained high and similar across groups (21 cases per 100 person-years for rectal gonorrhoea and 28 cases per 100 person-years for rectal chlamydia). Emtricitabine and tenofovir alafenamide continued to show superiority over emtricitabine and tenofovir disoproxil fumarate in all but one of the six prespecified bone mineral density and renal biomarkers. There was more weight gain among participants who had received emtricitabine and tenofovir alafenamide (median weight gain 1·7 kg vs 0·5 kg, p<0·0001).FINDINGSBetween Sept 13, 2016, and June 30, 2017, 5387 participants were randomly assigned to receive emtricitabine and tenofovir alafenamide (n=2694) or emtricitabine and tenofovir disoproxil fumarate (n=2693), contributing 10 081 person-years of follow-up. At 96 weeks of follow-up, there were eight HIV infections in participants who had received emtricitabine and tenofovir alafenamide (0·16 infections per 100 person-years [95% CI 0·07-0·31]) and 15 in participants who had received emtricitabine and tenofovir disoproxil fumarate (0·30 infections per 100 person-years [0·17-0·49]). Emtricitabine and tenofovir alafenamide maintained its non-inferiority to emtricitabine and tenofovir disoproxil fumarate for HIV prevention (IRR 0·54 [95% CI 0·23-1·26]). Approximately 78-82% of participants reported taking study medication more than 95% of the time across all study visits. Rates of sexually transmitted infections remained high and similar across groups (21 cases per 100 person-years for rectal gonorrhoea and 28 cases per 100 person-years for rectal chlamydia). Emtricitabine and tenofovir alafenamide continued to show superiority over emtricitabine and tenofovir disoproxil fumarate in all but one of the six prespecified bone mineral density and renal biomarkers. There was more weight gain among participants who had received emtricitabine and tenofovir alafenamide (median weight gain 1·7 kg vs 0·5 kg, p<0·0001).Emtricitabine and tenofovir alafenamide is safe and effective for longer-term pre-exposure prophylaxis in cisgender men and transgender women who have sex with men.INTERPRETATIONEmtricitabine and tenofovir alafenamide is safe and effective for longer-term pre-exposure prophylaxis in cisgender men and transgender women who have sex with men.Gilead Sciences.FUNDINGGilead Sciences.
In DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil fumarate showed non-inferior efficacy for HIV prevention and improved bone mineral density and renal safety biomarkers at week 48. We report outcomes analysed after all participants had completed 96 weeks of follow-up. This study is an ongoing, randomised, double-blind, multicentre, active-controlled, phase 3, non-inferiority trial done at 94 community, public health, and hospital-associated clinics located in Europe and North America. Adult cisgender men and transgender women who have sex with men, both with a high risk of acquiring HIV as determined by self-reported sexual behaviour or recent sexually transmitted infections, were randomly assigned (1:1) to receive either emtricitabine and tenofovir alafenamide (200/25 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir alafenamide group), or emtricitabine and tenofovir disoproxil fumarate (200/300 mg) tablets daily, with matched placebo tablets (emtricitabine and tenofovir disoproxil fumarate group). The primary efficacy outcome was incident HIV infection. Incidence of HIV-1 infection per 100 person-years was assessed when the last participant had completed 96 weeks of follow-up. This trial is registered with ClinicalTrials.gov, number NCT02842086. Between Sept 13, 2016, and June 30, 2017, 5387 participants were randomly assigned to receive emtricitabine and tenofovir alafenamide (n=2694) or emtricitabine and tenofovir disoproxil fumarate (n=2693), contributing 10 081 person-years of follow-up. At 96 weeks of follow-up, there were eight HIV infections in participants who had received emtricitabine and tenofovir alafenamide (0·16 infections per 100 person-years [95% CI 0·07-0·31]) and 15 in participants who had received emtricitabine and tenofovir disoproxil fumarate (0·30 infections per 100 person-years [0·17-0·49]). Emtricitabine and tenofovir alafenamide maintained its non-inferiority to emtricitabine and tenofovir disoproxil fumarate for HIV prevention (IRR 0·54 [95% CI 0·23-1·26]). Approximately 78-82% of participants reported taking study medication more than 95% of the time across all study visits. Rates of sexually transmitted infections remained high and similar across groups (21 cases per 100 person-years for rectal gonorrhoea and 28 cases per 100 person-years for rectal chlamydia). Emtricitabine and tenofovir alafenamide continued to show superiority over emtricitabine and tenofovir disoproxil fumarate in all but one of the six prespecified bone mineral density and renal biomarkers. There was more weight gain among participants who had received emtricitabine and tenofovir alafenamide (median weight gain 1·7 kg vs 0·5 kg, p<0·0001). Emtricitabine and tenofovir alafenamide is safe and effective for longer-term pre-exposure prophylaxis in cisgender men and transgender women who have sex with men. Gilead Sciences.
Author Ogbuagu, Onyema
Salazar, Laura C
Spinner, Christoph D
Kronborg, Gitte
Ruane, Peter J
Gilson, Richard
Brainard, Diana M
Shao, Yongwu
Asmuth, David M
Brunetta, Jason M
Wohl, David
Henry, Keith
Carter, Christoph
Cox, Stephanie
Whitlock, Gary
Podzamczer, Daniel
Kintu, Alexander
Das, Moupali
Baeten, Jared M
Ebrahimi, Ramin
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  givenname: Onyema
  surname: Ogbuagu
  fullname: Ogbuagu, Onyema
  email: onyema.ogbuagu@yale.edu
  organization: School of Medicine, Yale University, New Haven, CT, USA. Electronic address: onyema.ogbuagu@yale.edu
– sequence: 2
  givenname: Peter J
  surname: Ruane
  fullname: Ruane, Peter J
  organization: Ruane Clinical Research, Los Angeles, CA, USA
– sequence: 3
  givenname: Daniel
  surname: Podzamczer
  fullname: Podzamczer, Daniel
  organization: HIV and STI Unit, Infectious Disease Department, Hospital Universitario de Bellvitge, Barcelona, Spain
– sequence: 4
  givenname: Laura C
  surname: Salazar
  fullname: Salazar, Laura C
  organization: Hoag Medical Group, Newport Beach, CA, USA
– sequence: 5
  givenname: Keith
  surname: Henry
  fullname: Henry, Keith
  organization: Hennepin Healthcare Research Institute, Minneapolis, MN, USA
– sequence: 6
  givenname: David M
  surname: Asmuth
  fullname: Asmuth, David M
  organization: School of Medicine, University of California Davis, Davis, CA, USA
– sequence: 7
  givenname: David
  surname: Wohl
  fullname: Wohl, David
  organization: Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
– sequence: 8
  givenname: Richard
  surname: Gilson
  fullname: Gilson, Richard
  organization: Centre for Clinical Research in Infection and Sexual Health, University College London, London, UK
– sequence: 9
  givenname: Yongwu
  surname: Shao
  fullname: Shao, Yongwu
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 10
  givenname: Ramin
  surname: Ebrahimi
  fullname: Ebrahimi, Ramin
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 11
  givenname: Stephanie
  surname: Cox
  fullname: Cox, Stephanie
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 12
  givenname: Alexander
  surname: Kintu
  fullname: Kintu, Alexander
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 13
  givenname: Christoph
  surname: Carter
  fullname: Carter, Christoph
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 14
  givenname: Moupali
  surname: Das
  fullname: Das, Moupali
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 15
  givenname: Jared M
  surname: Baeten
  fullname: Baeten, Jared M
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 16
  givenname: Diana M
  surname: Brainard
  fullname: Brainard, Diana M
  organization: Departments of Biometrics, Virology, and Clinical Research, Gilead Sciences, Foster City, CA, USA
– sequence: 17
  givenname: Gary
  surname: Whitlock
  fullname: Whitlock, Gary
  organization: Chelsea and Westminster Hospital NHS Foundation Trust, London, UK
– sequence: 18
  givenname: Jason M
  surname: Brunetta
  fullname: Brunetta, Jason M
  organization: Maple Leaf Medical Clinic, Toronto, ON, Canada
– sequence: 19
  givenname: Gitte
  surname: Kronborg
  fullname: Kronborg, Gitte
  organization: Department of Infectious Diseases, University of Copenhagen, Hvidovre Hospital, Denmark
– sequence: 20
  givenname: Christoph D
  surname: Spinner
  fullname: Spinner, Christoph D
  organization: Technical University of Munich, Munich, Germany
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34197772$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Contributor Mayer, Kenneth
Benson, Paul
Hodge, Jr, Theo
Voskuhl, Gene
Berhe, Mezgebe
Lucasti, Christopher
Mills, Anthony
Leen, Clifford
Martorell, Claudia
Tremblay, Cecile
Larsen, Olav Ditlevsen
de Wet, Joseph
Ogbuagu, Onyema
Creticos, Catherine
Phoenix, John
Kronborg, Gitte
Shalit, Peter
Gerstoft, Jan
Szabo, Jason
Gilson, Richard
Grossberg, Robert
Mounzer, Karam
Gallant, Joel
Podzamczer, Daniel
Salazar, Laura
Bergin, Colm
Jessen, Heiko
Rashbaum, Bruce
Stephens, Jeffrey
Flamm, Jason
Mannheimer, Sharon
Knecht, Gabriele
Hare, Charles
LaMarca, Anthony
Markowitz, Martin
Apea, Vanessa
Grant, Robert
Antinori, Andrea
Larsen, Carsten Schade
Campbell, Thomas
Henry, William
Kegg, Stephen
Coll, Josep
Donovan, Taylor
Nwokolo, Nneka
Molina, Jean-Michel
Daar, Eric
Hengel, Richard
Ramgopal, Moti
Doblecki-Lewis, Susanne
Brar, Indira
Dosekun, Olamide
Halperin, Jason
Morris, Sheldon
Prins, Maria
Scott, Mia
Cruickshank, Frederick
Hurt, Christopher
Ruane, Peter
Cespedes, Michelle
Hosek, Sybil
Wohl, David
Osiyemi, Olayemi
Hardy, W David
Lazzarin, Adriano
Sobieszczyk, Magdalena
Reeve
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References 34571044 - Lancet HIV. 2021 Dec;8(12):e734. doi: 10.1016/S2352-3018(21)00264-2.
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Snippet In DISCOVER, a multinational, randomised controlled trial, emtricitabine and tenofovir alafenamide compared with emtricitabine and tenofovir disoproxil...
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SubjectTerms Adenine - adverse effects
Adenine - analogs & derivatives
Adenine - therapeutic use
Adult
Aged
Alanine - adverse effects
Alanine - therapeutic use
Anti-HIV Agents - adverse effects
Anti-HIV Agents - therapeutic use
Double-Blind Method
Drug Therapy, Combination - adverse effects
Emtricitabine - adverse effects
Emtricitabine - therapeutic use
Female
Follow-Up Studies
HIV Infections - prevention & control
HIV Infections - virology
HIV-1 - drug effects
HIV-1 - physiology
Humans
Male
Middle Aged
Organophosphonates - adverse effects
Organophosphonates - therapeutic use
Pre-Exposure Prophylaxis
Tenofovir - adverse effects
Tenofovir - therapeutic use
Treatment Outcome
Young Adult
Title Long-term safety and efficacy of emtricitabine and tenofovir alafenamide vs emtricitabine and tenofovir disoproxil fumarate for HIV-1 pre-exposure prophylaxis: week 96 results from a randomised, double-blind, placebo-controlled, phase 3 trial
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