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Doxycycline to prevent bacterial sexually transmitted infections in the USA: final results from the DoxyPEP multicentre, open-label, randomised controlled trial and open-label extension
by
Buchbinder, Susan P
, Havlir, Diane V
, Vittinghoff, Eric
, Lopez, Carolina
, Soge, Olusegun O
, Dombrowski, Julia C
, Grabow, Cole
, Suchland, Robert J
, Haser, Grace
, Celum, Connie
, Malinski, Cheryl
, Nasser, Melody
, Cannon, Chase
, Charlebois, Edwin D
, Donnell, Deborah
, Perkins, Rodney
, Cohen, Stephanie E
, Brown, Clare
, Luetkemeyer, Anne F
, Scott, Hyman
in
Adolescent
/ Adult
/ Adverse events
/ Anti-Bacterial Agents - administration & dosage
/ Anti-Bacterial Agents - therapeutic use
/ Antimicrobial agents
/ Antimicrobial resistance
/ Antiretroviral drugs
/ Bacteria
/ Bacterial infections
/ Chlamydia
/ Chlamydia Infections - epidemiology
/ Chlamydia Infections - prevention & control
/ Cisgender
/ Disease prevention
/ Doxycycline
/ Doxycycline - administration & dosage
/ Doxycycline - therapeutic use
/ Drug resistance
/ Effectiveness
/ Female
/ Gonorrhea
/ Gonorrhea - epidemiology
/ Gonorrhea - prevention & control
/ HIV
/ Homosexuality, Male
/ Human immunodeficiency virus
/ Humans
/ Incidence
/ Infections
/ Labels
/ Male
/ Men
/ Middle Aged
/ Minimum inhibitory concentration
/ Prophylaxis
/ Public health
/ Review boards
/ San Francisco - epidemiology
/ Sex
/ Sexual behavior
/ Sexual health
/ Sexually transmitted diseases
/ Sexually Transmitted Diseases - epidemiology
/ Sexually Transmitted Diseases - prevention & control
/ Sexually Transmitted Diseases, Bacterial - epidemiology
/ Sexually Transmitted Diseases, Bacterial - prevention & control
/ STD
/ Syphilis
/ Transgender Persons
/ Washington - epidemiology
/ Women
/ Young Adult
2025
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Doxycycline to prevent bacterial sexually transmitted infections in the USA: final results from the DoxyPEP multicentre, open-label, randomised controlled trial and open-label extension
by
Buchbinder, Susan P
, Havlir, Diane V
, Vittinghoff, Eric
, Lopez, Carolina
, Soge, Olusegun O
, Dombrowski, Julia C
, Grabow, Cole
, Suchland, Robert J
, Haser, Grace
, Celum, Connie
, Malinski, Cheryl
, Nasser, Melody
, Cannon, Chase
, Charlebois, Edwin D
, Donnell, Deborah
, Perkins, Rodney
, Cohen, Stephanie E
, Brown, Clare
, Luetkemeyer, Anne F
, Scott, Hyman
in
Adolescent
/ Adult
/ Adverse events
/ Anti-Bacterial Agents - administration & dosage
/ Anti-Bacterial Agents - therapeutic use
/ Antimicrobial agents
/ Antimicrobial resistance
/ Antiretroviral drugs
/ Bacteria
/ Bacterial infections
/ Chlamydia
/ Chlamydia Infections - epidemiology
/ Chlamydia Infections - prevention & control
/ Cisgender
/ Disease prevention
/ Doxycycline
/ Doxycycline - administration & dosage
/ Doxycycline - therapeutic use
/ Drug resistance
/ Effectiveness
/ Female
/ Gonorrhea
/ Gonorrhea - epidemiology
/ Gonorrhea - prevention & control
/ HIV
/ Homosexuality, Male
/ Human immunodeficiency virus
/ Humans
/ Incidence
/ Infections
/ Labels
/ Male
/ Men
/ Middle Aged
/ Minimum inhibitory concentration
/ Prophylaxis
/ Public health
/ Review boards
/ San Francisco - epidemiology
/ Sex
/ Sexual behavior
/ Sexual health
/ Sexually transmitted diseases
/ Sexually Transmitted Diseases - epidemiology
/ Sexually Transmitted Diseases - prevention & control
/ Sexually Transmitted Diseases, Bacterial - epidemiology
/ Sexually Transmitted Diseases, Bacterial - prevention & control
/ STD
/ Syphilis
/ Transgender Persons
/ Washington - epidemiology
/ Women
/ Young Adult
2025
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Doxycycline to prevent bacterial sexually transmitted infections in the USA: final results from the DoxyPEP multicentre, open-label, randomised controlled trial and open-label extension
by
Buchbinder, Susan P
, Havlir, Diane V
, Vittinghoff, Eric
, Lopez, Carolina
, Soge, Olusegun O
, Dombrowski, Julia C
, Grabow, Cole
, Suchland, Robert J
, Haser, Grace
, Celum, Connie
, Malinski, Cheryl
, Nasser, Melody
, Cannon, Chase
, Charlebois, Edwin D
, Donnell, Deborah
, Perkins, Rodney
, Cohen, Stephanie E
, Brown, Clare
, Luetkemeyer, Anne F
, Scott, Hyman
in
Adolescent
/ Adult
/ Adverse events
/ Anti-Bacterial Agents - administration & dosage
/ Anti-Bacterial Agents - therapeutic use
/ Antimicrobial agents
/ Antimicrobial resistance
/ Antiretroviral drugs
/ Bacteria
/ Bacterial infections
/ Chlamydia
/ Chlamydia Infections - epidemiology
/ Chlamydia Infections - prevention & control
/ Cisgender
/ Disease prevention
/ Doxycycline
/ Doxycycline - administration & dosage
/ Doxycycline - therapeutic use
/ Drug resistance
/ Effectiveness
/ Female
/ Gonorrhea
/ Gonorrhea - epidemiology
/ Gonorrhea - prevention & control
/ HIV
/ Homosexuality, Male
/ Human immunodeficiency virus
/ Humans
/ Incidence
/ Infections
/ Labels
/ Male
/ Men
/ Middle Aged
/ Minimum inhibitory concentration
/ Prophylaxis
/ Public health
/ Review boards
/ San Francisco - epidemiology
/ Sex
/ Sexual behavior
/ Sexual health
/ Sexually transmitted diseases
/ Sexually Transmitted Diseases - epidemiology
/ Sexually Transmitted Diseases - prevention & control
/ Sexually Transmitted Diseases, Bacterial - epidemiology
/ Sexually Transmitted Diseases, Bacterial - prevention & control
/ STD
/ Syphilis
/ Transgender Persons
/ Washington - epidemiology
/ Women
/ Young Adult
2025
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Doxycycline to prevent bacterial sexually transmitted infections in the USA: final results from the DoxyPEP multicentre, open-label, randomised controlled trial and open-label extension
Journal Article
Doxycycline to prevent bacterial sexually transmitted infections in the USA: final results from the DoxyPEP multicentre, open-label, randomised controlled trial and open-label extension
2025
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Overview
Doxycycline post-exposure prophylaxis (doxy-PEP) is a promising intervention to reduce bacterial sexually transmitted infections (STIs). We evaluated the effect of doxy-PEP on STI incidence and antimicrobial resistance in men who have sex with men and transgender women for up to 12 months of follow-up, inlcuding an open-label extension.
DoxyPEP, an open-label trial in Seattle (WA, USA) and San Francisco (CA, USA) among men who have sex with men and transgender women with at least one bacterial STI in the past year, randomly assigned participants by clinic (with computer-generated variable block sizes) 2:1 to doxy-PEP (200 mg doxycycline delayed-release tablets 24–72 h after condomless sex) or standard care. The independent endpoint adjudication committee was masked to group assignment. The primary outcome was presence of one or more bacterial STIs (Neisseria gonorrhoeae, Chlamydia trachomatis, or early syphilis) each quarter. This outcome was assessed in the modified intention-to-treat cohort, which included participants with at least one follow-up quarter (ie, ∼3 months) in their as-randomised assignment. After early termination of the randomised phase for efficacy, all participants still enrolled were offered doxy-PEP in an open-label extension (OLE). We report quarterly incidence of bacterial STIs for the as-randomised and OLE periods. Safety was assessed in all participants with any follow-up data. The trial was registered with ClinicalTrials.gov (NCT03980223) and is completed.
From Aug 19, 2020, to May 13, 2022, we enrolled 637 participants; 592 participants completed at least one follow-up quarter in the randomised phase (411 in the doxy-PEP group and 181 in the standard-care group) and 282 in the OLE phase (207 in the doxy-PEP group and 82 in the standard-care group). STIs were present in 129 (12·0%) of 1077 quarters in the doxy-PEP group versus 139 (30·5%) of 455 quarters in the standard-care group during the as-randomised period, showing an absolute difference of 19 percentage points and a relative risk of 0·39 (95% CI 0·31–0·49, p<0·0001). During the OLE, STIs were diagnosed in 51 (13%) of 388 quarters among those continuing doxy-PEP and 25 (17%) of 145 quarters among standard-care participants who initiated doxy-PEP. Throughout all quarters for participants on doxy-PEP, there was one grade 2 laboratory abnormality and five grade 3 adverse events that were possibly or probably related to doxy-PEP. No serious adverse events were attributed by site investigators to doxycycline. Of participants with positive gonorrhoea cultures during the study, eight (27%) of 29 taking doxy-PEP versus five (24%) of 21 not taking doxy-PEP had tetracycline resistance (minimum inhibitory concentration ≥2 μg/mL).
Doxy-PEP was effective in reducing bacterial STIs in this population of men who have sex with men and transgender women, including during an open-label extension when doxy-PEP efficacy was known. Doxy-PEP was well tolerated, highly acceptable, and with no new safety signals.
US National Institutes of Health.
Publisher
Elsevier Ltd,Elsevier Limited
Subject
/ Adult
/ Anti-Bacterial Agents - administration & dosage
/ Anti-Bacterial Agents - therapeutic use
/ Bacteria
/ Chlamydia Infections - epidemiology
/ Chlamydia Infections - prevention & control
/ Doxycycline - administration & dosage
/ Doxycycline - therapeutic use
/ Female
/ Gonorrhea - prevention & control
/ HIV
/ Human immunodeficiency virus
/ Humans
/ Labels
/ Male
/ Men
/ Minimum inhibitory concentration
/ San Francisco - epidemiology
/ Sex
/ Sexually transmitted diseases
/ Sexually Transmitted Diseases - epidemiology
/ Sexually Transmitted Diseases - prevention & control
/ Sexually Transmitted Diseases, Bacterial - epidemiology
/ Sexually Transmitted Diseases, Bacterial - prevention & control
/ STD
/ Syphilis
/ Women
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