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<channel>
	<title>Publication &#8211; GARDP</title>
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	<link>https://gardp.org</link>
	<description>Global Antibiotic Research and Development Partnership</description>
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	<title>Publication &#8211; GARDP</title>
	<link>https://gardp.org</link>
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	<item>
		<title>In vitro activity of zoliflodacin against Neisseria gonorrhoeae collected in the United States from 2020 to 2022</title>
		<link>https://gardp.org/in-vitro-activity-of-zoliflodacin-against-neisseria-gonorrhoeae-collected-in-the-united-states-from-2020-to-2022/</link>
		
		<dc:creator><![CDATA[gabrielle]]></dc:creator>
		<pubDate>Mon, 03 Aug 2026 12:53:31 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/?p=7007</guid>

					<description><![CDATA[Zoliflodacin is a first-in-class spiropyrimidinetrione, oral, single-dose antibacterial recently approved by the US FDA for treatment of uncomplicated urogenital gonorrhea. Isolates of Neisseria gonorrhoeae (n = 322) collected in the United States in 2020–2022 by the Centers for Disease Control and Prevention, as well as two ceftriaxone-resistant isolates, were tested for susceptibility to zoliflodacin. All [&#8230;]]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">Zoliflodacin is a first-in-class spiropyrimidinetrione, oral, single-dose antibacterial recently approved by the US FDA for treatment of uncomplicated urogenital gonorrhea. Isolates of <em>Neisseria gonorrhoeae </em>(<em>n</em> = 322) collected in the United States in 2020–2022 by the Centers for Disease Control and Prevention, as well as two ceftriaxone-resistant isolates, were tested for susceptibility to zoliflodacin. All isolates were susceptible to zoliflodacin with MIC50/90 values of 0.12 µg/mL. Zoliflodacin activity was consistent over time and against ceftriaxone-, ciprofloxacin-, and tetracycline-resistant and azithromycin-non-susceptible isolates.</p>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Sarah M. McLeod, Samir H. Moussa, Meredith Hackel, Carmen Au, Pierre Daram</p>



<p class="wp-block-paragraph"></p>



<div class="wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex">
<div class="wp-block-button has-arrow"><a class="wp-block-button__link has-custom-off-black-color has-gardp-blue-background-color has-text-color has-background has-link-color has-border-color has-gardp-blue-border-color wp-element-button" href="https://doi.org/10.1128/aac.00527-26" target="_blank" rel="noreferrer noopener">READ PUBLICATION</a></div>
</div>



<p class="wp-block-paragraph"></p>

<p><a href="https://gardp.org/in-vitro-activity-of-zoliflodacin-against-neisseria-gonorrhoeae-collected-in-the-united-states-from-2020-to-2022/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Access to Reserve Antibiotics in Latin America and the Caribbean: Situation, Challenges, and Future Directions</title>
		<link>https://gardp.org/access-to-reserve-antibiotics-in-latin-america-and-the-caribbean-situation-challenges-and-future-directions/</link>
		
		<dc:creator><![CDATA[gabrielle]]></dc:creator>
		<pubDate>Wed, 22 Jul 2026 09:59:39 +0000</pubDate>
				<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/?p=6840</guid>

					<description><![CDATA[Access to Reserve antibiotics, which are defined by the World Health Organization’s AWaRe (Access, Watch, Reserve) classification framework as last-resort treatments for multidrug-resistant infections, remains poorly documented in Latin America and the Caribbean despite evidence of increasing antimicrobial resistance in the region, with associated and attributable mortality projected to rise. We examined the landscape of [&#8230;]]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">Access to Reserve antibiotics, which are defined by the World Health Organization’s AWaRe (Access, Watch, Reserve) classification framework as last-resort treatments for multidrug-resistant infections, remains poorly documented in Latin America and the Caribbean despite evidence of increasing antimicrobial resistance in the region, with associated and attributable mortality projected to rise. We examined the landscape of Reserve antibiotic access across Latin America and the Caribbean, identifying the systematic barriers that prevent patients from receiving appropriate treatment. We found that multiple interconnected obstacles—spanning regulatory approval, manufacturer participation, formulary inclusion, procurement systems, and health technology assessment capacity—create compounding delays and gaps in access.</p>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Susana Ribeiro, Yanina Nuccetelli, Wanda Cornistein, Maria Ines Staneloni</p>



<div class="wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex">
<div class="wp-block-button"><a class="wp-block-button__link has-custom-off-black-color has-gardp-blue-background-color has-text-color has-background has-link-color has-border-color has-gardp-blue-border-color wp-element-button" href="https://doi.org/10.2147/IDR.S547524" target="_blank" rel="noreferrer noopener">READ PUBLICATION</a></div>
</div>



<p class="wp-block-paragraph"></p>

<p><a href="https://gardp.org/access-to-reserve-antibiotics-in-latin-america-and-the-caribbean-situation-challenges-and-future-directions/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>GARDP joins seven other Product Development Partnerships in call for sustained EU investment in EDCTP</title>
		<link>https://gardp.org/gardp-joins-seven-other-product-development-partnerships-in-call-for-sustained-eu-investment-in-edctp/</link>
		
		<dc:creator><![CDATA[Hasina Khatun]]></dc:creator>
		<pubDate>Mon, 29 Jun 2026 09:37:26 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/?p=5956</guid>

					<description><![CDATA[GARDP has joined seven other Product Development Partnerships (PDPs) in calling for sustained investment in the European and Developing Countries Clinical Trials Partnership (EDCTP) under the next EU Framework Programme for Research and Innovation and other EU funding frameworks currently under discussion. For more than 20 years, EDCTP has demonstrated the impact of Europe–Africa collaboration [&#8230;]]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">GARDP has joined seven other Product Development Partnerships (PDPs) in calling for sustained investment in the European and Developing Countries Clinical Trials Partnership (EDCTP) under the next EU Framework Programme for Research and Innovation and other EU funding frameworks currently under discussion.</p>



<p class="wp-block-paragraph">For more than 20 years, EDCTP has demonstrated the impact of Europe–Africa collaboration — supporting clinical research, strengthening scientific capacity and accelerating the development of health innovations that address poverty-related and neglected diseases. Beyond its role as a research funding instrument, EDCTP serves as a strategic platform connecting Europe&#8217;s global health, research and innovation agendas.</p>



<p class="wp-block-paragraph">As global health challenges evolve, continued investment in EDCTP will be essential to ensure Europe and Africa remain at the forefront of discovery, innovation and preparedness for emerging threats.</p>



<p class="wp-block-paragraph">Read more about the impact of the collaboration between PDPs and EDCTP, and our joint recommendations, in the new report.</p>



<p class="wp-block-paragraph"> </p>



<div class="wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex">
<div class="wp-block-button has-arrow"><a class="wp-block-button__link has-gardp-dark-color has-gardp-blue-background-color has-text-color has-background has-link-color has-border-color has-gardp-blue-border-color wp-element-button" href="https://gardp.org/wp-content/uploads/2026/07/EDCTP-PDP-Advocacy-Paper_20260625.pdf">READ THE PAPER</a></div>
</div>



<p class="wp-block-paragraph"></p>

<p><a href="https://gardp.org/gardp-joins-seven-other-product-development-partnerships-in-call-for-sustained-eu-investment-in-edctp/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Diagnostics for priority bacterial pathogens: global gaps and research needs for curbing antimicrobial resistance in low-resource settings</title>
		<link>https://gardp.org/diagnostics-for-priority-bacterial-pathogens-global-gaps-and-research-needs-for-curbing-antimicrobial-resistance-in-low-resource-settings/</link>
		
		<dc:creator><![CDATA[Hasina Khatun]]></dc:creator>
		<pubDate>Fri, 20 Mar 2026 13:28:58 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/diagnostics-for-priority-bacterial-pathogens-global-gaps-and-research-needs-for-curbing-antimicrobial-resistance-in-low-resource-settings/</guid>

					<description><![CDATA[Antimicrobial resistance (AMR) is a major and growing threat to global health, development, and security, with the greatest burden borne by low-income and middle-income countries (LMICs). Without urgent intervention, cumulative deaths between 2020 and 2050, attributable to AMR, are projected to be 39·1 million globally. Effective diagnostics are important to bacterial pathogen detection and antimicrobial [&#8230;]]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image"><img fetchpriority="high" decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail-300x184.png" alt="Lancet MediaCoverage Thumbnail" class="wp-image-3758" srcset="https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail-300x184.png 300w, https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail.png 700w" sizes="(max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">Antimicrobial resistance (AMR) is a major and growing threat to global health, development, and security, with the greatest burden borne by low-income and middle-income countries (LMICs). Without urgent intervention, cumulative deaths between 2020 and 2050, attributable to AMR, are projected to be 39·1 million globally. Effective diagnostics are important to bacterial pathogen detection and antimicrobial susceptibility testing, and such diagnostics support antibiotic stewardship by reducing adverse drug events (eg, toxicity or allergy) and restricting the emergence and spread of AMR. Yet, access to appropriate diagnostics in LMICs remains constrained.</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Valeria Gigante PhD, Maurine Murtagh JD, Prof Till T Bachmann PhD, Tamarie Rocke MD, Betsy W Trainor BSc, Susan M Poutanen MD MPH, Teri Roberts PhD, Prof Jordi Vila MD PhD, Alexandra Cameron PhD</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><span style="text-decoration: underline;"><a href="https://doi.org/10.1016/j.lanmic.2026.101385" target="_blank" rel="noopener">Read publication</a></span></p>

<p><a href="https://gardp.org/diagnostics-for-priority-bacterial-pathogens-global-gaps-and-research-needs-for-curbing-antimicrobial-resistance-in-low-resource-settings/">Source</a></p>]]></content:encoded>
					
		
		
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		<item>
		<title>Evaluation of Drug–Drug Interaction Potential Between the Oral Antibiotic Zoliflodacin and the CYP3A4 Inhibitor Itraconazole: A Phase 1 Study in Healthy Participants</title>
		<link>https://gardp.org/evaluation-of-drug-drug-interaction-potential-between-the-oral-antibiotic-zoliflodacin-and-the-cyp3a4-inhibitor-itraconazole-a-phase-1-study-in-healthy-participants/</link>
		
		<dc:creator><![CDATA[Hasina Khatun]]></dc:creator>
		<pubDate>Fri, 27 Feb 2026 13:23:04 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/evaluation-of-drug-drug-interaction-potential-between-the-oral-antibiotic-zoliflodacin-and-the-cyp3a4-inhibitor-itraconazole-a-phase-1-study-in-healthy-participants/</guid>

					<description><![CDATA[Zoliflodacin is a first-in-class oral spiropyrimidinetrione antibiotic being developed for patients with uncomplicated gonorrhea, including those infected with multidrug-resistant strains. Because zoliflodacin is metabolized by cytochrome P450 3A4 (CYP3A4), concomitant administration with a CYP3A inhibitor has the potential to increase zoliflodacin plasma exposure. The aim of this phase 1 drug–drug interaction (DDI) study was to [&#8230;]]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image"><img decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2026/02/ASCPT-700-x-430-px-300x184.png" alt="ASCPT (700 x 430 px)" class="wp-image-4122" srcset="https://gardp.org/wp-content/uploads/2026/02/ASCPT-700-x-430-px-300x184.png 300w, https://gardp.org/wp-content/uploads/2026/02/ASCPT-700-x-430-px.png 700w" sizes="(max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">Zoliflodacin is a first-in-class oral spiropyrimidinetrione antibiotic being developed for patients with uncomplicated gonorrhea, including those infected with multidrug-resistant strains. Because zoliflodacin is metabolized by cytochrome P450 3A4 (CYP3A4), concomitant administration with a CYP3A inhibitor has the potential to increase zoliflodacin plasma exposure. The aim of this phase 1 drug–drug interaction (DDI) study was to assess the effect of the strong CYP3A4 inhibitor itraconazole on the pharmacokinetics (PK) and safety of a 3 g single oral dose of zoliflodacin.</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Alison Luckey, Kajal B. Larson, Noha Rayad, Markus Heep, Sophie Delhomme, Gabrielle Kornmann, John P. Mueller, John P. O&#8217;Donnell, Seamus O&#8217;Brien, Rainard Fuhr, Jean-Yves Gillon</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><span style="text-decoration: underline;"><a href="https://doi.org/10.1111/cts.70515" target="_blank" rel="noopener">Read publication</a></span></p>

<p><a href="https://gardp.org/evaluation-of-drug-drug-interaction-potential-between-the-oral-antibiotic-zoliflodacin-and-the-cyp3a4-inhibitor-itraconazole-a-phase-1-study-in-healthy-participants/">Source</a></p>]]></content:encoded>
					
		
		
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		<item>
		<title>Prevalence of Chlamydia trachomatis and Neisseria gonorrhoeae infections and associated risk factors among pregnant women and key populations in Kenya: A multi-centre cross-sectional study</title>
		<link>https://gardp.org/23296-2/</link>
		
		<dc:creator><![CDATA[Hasina Khatun]]></dc:creator>
		<pubDate>Tue, 24 Feb 2026 13:25:27 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/23296-2/</guid>

					<description><![CDATA[Sexually-transmitted pathogens&#160;Chlamydia trachomatis&#160;(CT) and&#160;Neisseria gonorrhoeae&#160;(NG) cause curable but often asymptomatic bacterial infections. Missed diagnoses and treatment, leading to chronic infections, can cause clinical complications and increase transmission. Accurate prevalence estimates are essential for the effective public health control of these sexually transmitted infections, especially in Africa, where data are scarce. &#160; Authors Catherine Ngugi,Borna A. [&#8230;]]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image"><img decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2026/02/PLOS-700-x-430-px-300x184.png" alt="PLOS (700 x 430 px)" class="wp-image-4126" srcset="https://gardp.org/wp-content/uploads/2026/02/PLOS-700-x-430-px-300x184.png 300w, https://gardp.org/wp-content/uploads/2026/02/PLOS-700-x-430-px.png 700w" sizes="(max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">Sexually-transmitted pathogens&nbsp;<em>Chlamydia trachomatis</em>&nbsp;(CT) and&nbsp;<em>Neisseria gonorrhoeae</em>&nbsp;(NG) cause curable but often asymptomatic bacterial infections. Missed diagnoses and treatment, leading to chronic infections, can cause clinical complications and increase transmission. Accurate prevalence estimates are essential for the effective public health control of these sexually transmitted infections, especially in Africa, where data are scarce.</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Catherine Ngugi,Borna A. Nyaoke,Leonard Kingwara,Pacific Akinyi,Mildred Mmbone,Thaddaeus W. Egondi,George M. Nyangweso,Helen Broadhurst,Gabrielle Kornmann,Rashmi Mathur ,Esther Bettiol</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><a href="https://doi.org/10.1371/journal.pgph.0005479" target="_blank" rel="noopener"><span style="text-decoration: underline;">Read publication</span></a></p>

<p><a href="https://gardp.org/23296-2/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>AntibioticDB: An Updated and Improved Open-Access Database for the Antibacterial Research and Development Community</title>
		<link>https://gardp.org/antibioticdb-an-updated-and-improved-open-access-database-for-the-antibacterial-research-and-development-community/</link>
		
		<dc:creator><![CDATA[gardpadm]]></dc:creator>
		<pubDate>Mon, 23 Feb 2026 14:25:02 +0000</pubDate>
				<category><![CDATA[GARDP Articles]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/antibioticdb-an-updated-and-improved-open-access-database-for-the-antibacterial-research-and-development-community/</guid>

					<description><![CDATA[AntibioticDB (https://www.antibioticdb.com/), originally established in 2017 and since 2021 led by the Global Antibiotic Research &#38; Development Partnership (GARDP), is a freely available database of antibacterial agents to facilitate research and development of new antibacterial therapeutics. Here, we describe a new release of AntibioticDB that has been significantly expanded and updated with the aid of [&#8230;]]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image"><img loading="lazy" decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2026/02/ACS-Pub700-x-430-px-300x184.png" alt="ACS Pub(700 x 430 px)" class="wp-image-4130" srcset="https://gardp.org/wp-content/uploads/2026/02/ACS-Pub700-x-430-px-300x184.png 300w, https://gardp.org/wp-content/uploads/2026/02/ACS-Pub700-x-430-px.png 700w" sizes="auto, (max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">AntibioticDB (<a href="https://www.antibioticdb.com/" target="_blank" rel="noopener">https://www.antibioticdb.com/</a>), originally established in 2017 and since 2021 led by the Global Antibiotic Research &amp; Development Partnership (GARDP), is a freely available database of antibacterial agents to facilitate research and development of new antibacterial therapeutics. Here, we describe a new release of AntibioticDB that has been significantly expanded and updated with the aid of user feedback and which offers additional functionality through a redesigned web portal.</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Luiza H. Galarion, Alan Hennessy, Simon D. Harding, Jane F. Armstrong, Astrid Pentz-Murr, Jamie A. Davies, Alex J. O’Neill, Laura J. V. Piddock</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><a href="https://pubs.acs.org/doi/10.1021/acsinfecdis.5c00955" target="_blank" rel="noopener">Read full article</a></p>

<p><a href="https://gardp.org/antibioticdb-an-updated-and-improved-open-access-database-for-the-antibacterial-research-and-development-community/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Pharmacokinetics and safety of fosfomycin and flomoxef administered as part of neonatal sepsis treatment (NeoSep1 Part 1)</title>
		<link>https://gardp.org/pharmacokinetics-and-safety-of-fosfomycin-and-flomoxefadministered-as-part-of-neonatal-sepsis-treatment-neosep1-part-1/</link>
		
		<dc:creator><![CDATA[gardpadm]]></dc:creator>
		<pubDate>Mon, 29 Dec 2025 14:49:03 +0000</pubDate>
				<category><![CDATA[GARDP Articles]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/pharmacokinetics-and-safety-of-fosfomycin-and-flomoxefadministered-as-part-of-neonatal-sepsis-treatment-neosep1-part-1/</guid>

					<description><![CDATA[Neonatal doses for the off-patent antibiotics fosfomycin and flomoxef, flomoxef,which offer coverage against many extended-spectrum beta-lactamase (ESBL)-producing organisms, are based on limited data. We performed a pharmacokinetic (PK) and safety study of fosfomycin and flomoxef to confirm proposed neonatal dosing before further investigation in a trial (NeoSep1, ISRCTN48721236). Authors Adrie Bekker, Navarat Panjasawatwong, Louise F. [&#8230;]]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image"><img loading="lazy" decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2025/12/ASM-700-x-430-px-300x184.png" alt="ASM (700 x 430 px)" class="wp-image-4132" srcset="https://gardp.org/wp-content/uploads/2025/12/ASM-700-x-430-px-300x184.png 300w, https://gardp.org/wp-content/uploads/2025/12/ASM-700-x-430-px.png 700w" sizes="auto, (max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">Neonatal doses for the off-patent antibiotics fosfomycin and flomoxef, flomoxef,which offer coverage against many extended-spectrum beta-lactamase (ESBL)-producing organisms, are based on limited data. We performed a pharmacokinetic (PK) and safety study of fosfomycin and flomoxef to confirm proposed neonatal dosing before further investigation in a trial (NeoSep1, ISRCTN48721236).</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Adrie Bekker, Navarat Panjasawatwong, Louise F. Hill, Wolfgang Stohr, A. Sarah Walker, Sally Ellis, Angela Dramowski, Andrew Whitelaw, Christina Obiero, James A. Berkley, Alexander Makazi, Sithembiso Velaphi, Reenu Thomas, Petronella Magagula, Ilhaam Abrahams, Firdose L. Nakwa, Mohammed M. Barday, Alison Van Kwawegen, Kamla Pillay, Silke Gastine, Joseph F. Standing, Peter Skoutari, Francesca Schiavone, Mike Sharland, Seamus O’Brien, Julia A. Bielicki, Tim R. Cressey, On behalf of the NeoSep Study Team</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><a href="https://journals.asm.org/doi/10.1128/aac.01126-25" target="_blank" rel="noopener">Read full publication</a></p>

<p><a href="https://gardp.org/pharmacokinetics-and-safety-of-fosfomycin-and-flomoxefadministered-as-part-of-neonatal-sepsis-treatment-neosep1-part-1/">Source</a></p>]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>Zoliflodacin versus ceftriaxone plus azithromycin for treatment of uncomplicated urogenital gonorrhoea: an international, randomised, controlled, open-label, phase 3, non-inferiority clinical trial</title>
		<link>https://gardp.org/zoliflodacin-versus-ceftriaxone-plus-azithromycin-for-treatment-of-uncomplicated-urogenital-gonorrhoea-an-international-randomised-controlled-open-label-phase-3-non-inferiority-clinical-trial/</link>
		
		<dc:creator><![CDATA[gardpadm]]></dc:creator>
		<pubDate>Thu, 11 Dec 2025 23:32:56 +0000</pubDate>
				<category><![CDATA[GARDP Publications]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/zoliflodacin-versus-ceftriaxone-plus-azithromycin-for-treatment-of-uncomplicated-urogenital-gonorrhoea-an-international-randomised-controlled-open-label-phase-3-non-inferiority-clinical-trial/</guid>

					<description><![CDATA[In 2020, WHO estimated that Neisseria gonorrhoeae caused 82·4 million new cases of gonorrhoea among those aged 15–49 years worldwide. Without effective treatment, the morbidity associated with gonorrhoea complications can be considerable. Additionally, N gonorrhoeae infection enhances the risk of acquiring or transmitting HIV. N gonorrhoeae has developed resistance to all current and previously used [&#8230;]]]></description>
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<figure class="wp-block-image"><img loading="lazy" decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail-300x184.png" alt="Lancet MediaCoverage Thumbnail" class="wp-image-3758" srcset="https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail-300x184.png 300w, https://gardp.org/wp-content/uploads/2024/10/Lancet-MediaCoverage-Thumbnail.png 700w" sizes="auto, (max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">In 2020, WHO estimated that <em>Neisseria gonorrhoeae</em> caused 82·4 million new cases of gonorrhoea among those aged 15–49 years worldwide. Without effective treatment, the morbidity associated with gonorrhoea complications can be considerable. Additionally, <em>N gonorrhoeae</em> infection enhances the risk of acquiring or transmitting HIV.</p>



<p class="wp-block-paragraph"><em>N gonorrhoeae</em> has developed resistance to all current and previously used classes of antibiotics used to treat gonorrhoea, with ceftriaxone the sole remaining empirical treatment option for first-line gonorrhoea monotherapy. In 2017–18, the WHO Gonococcal Antimicrobial Surveillance Programme (GASP) reported high global rates of fluoroquinolone resistance, increasing azithromycin resistance, and, worryingly, progressively increasing multidrug resistance, including to extended-spectrum cephalosporins, such as ceftriaxone. Resistance patterns vary considerably by region; the WHO Enhanced GASP has highlighted situations of particular concern in Cambodia and Viet Nam. In 2022, nearly a third of isolates (32%) in Cambodia showed resistance to either broad-spectrum cephalosporins or azithromycin (with 7% showing resistance to both), and in Viet Nam, 27% of isolates were resistant to ceftriaxone in 2023. The WHO global action plan highlighted the development of new antibiotics for gonorrhoea as a high priority, and in 2019 the US Centers for Disease Control and Prevention declared antimicrobial-resistant <em>N gonorrhoeae</em> an urgent public health threat.</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph">Alison Luckey, Manica Balasegaram, Lindley A Barbee, Teresa A Batteiger, Helen Broadhurst, Stephanie E Cohen, Sinead Delany-Moretlwe, Henry J C de Vries, Jodie A Dionne, Katherine Gill, Chris Kenyon, Rossaphorn Kittiyaowamarn, Drew Lewis, John P Mueller, Vimla Naicker, Seamus O’Brien, John P O’Donnell, Nittaya Phanuphak, Elizabeth Spooner, Subasree Srinivasan, Stephanie N Taylor, Magnus Unemo, Zinhle Zwane, Edward W Hook 3rd, for the Zoliflodacin Phase 3 Study Group*</p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><a href="https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(25)01953-1/fulltext" target="_blank" rel="noopener">Read the publication</a></p>

<p><a href="https://gardp.org/zoliflodacin-versus-ceftriaxone-plus-azithromycin-for-treatment-of-uncomplicated-urogenital-gonorrhoea-an-international-randomised-controlled-open-label-phase-3-non-inferiority-clinical-trial/">Source</a></p>]]></content:encoded>
					
		
		
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		<title>Carbapenem-resistant Enterobacterales among patients with bloodstream infections in South Africa: Consolidated surveillance data, 2015–2021</title>
		<link>https://gardp.org/carbapenem-resistant-enterobacterales-among-patients-with-bloodstream-infections-in-south-africa-consolidated-surveillance-data-2015-2021/</link>
		
		<dc:creator><![CDATA[Hasina Khatun]]></dc:creator>
		<pubDate>Thu, 03 Jul 2025 09:26:09 +0000</pubDate>
				<category><![CDATA[GARDP Articles]]></category>
		<category><![CDATA[Publication]]></category>
		<guid isPermaLink="false">https://gardp.org/carbapenem-resistant-enterobacterales-among-patients-with-bloodstream-infections-in-south-africa-consolidated-surveillance-data-2015-2021/</guid>

					<description><![CDATA[A fifth of blood cultures from patients with infections acquired in a healthcare setting in South Africa will yield an organism. Carbapenem-resistant Enterobacterales (CREs), specifically&#160;Klebsiella pneumoniae&#160;are the most predominant Gram-negative bacteria (GNB) isolated among bloodstream infections (BSI). Additionally, the multidrug-resistant nature of these organisms is not only a threat to patients but it also poses [&#8230;]]]></description>
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<figure class="wp-block-image"><img loading="lazy" decoding="async" width="300" height="184" src="https://gardp.org/wp-content/uploads/2025/07/PLOS-ONE-700-x-430-px-300x184.png" alt="PLOS ONE (700 x 430 px)" class="wp-image-4135" srcset="https://gardp.org/wp-content/uploads/2025/07/PLOS-ONE-700-x-430-px-300x184.png 300w, https://gardp.org/wp-content/uploads/2025/07/PLOS-ONE-700-x-430-px.png 700w" sizes="auto, (max-width: 300px) 100vw, 300px" /></figure>



<p class="wp-block-paragraph"></p>



<p class="wp-block-paragraph">A fifth of blood cultures from patients with infections acquired in a healthcare setting in South Africa will yield an organism. Carbapenem-resistant Enterobacterales (CREs), specifically&nbsp;<em>Klebsiella pneumoniae</em>&nbsp;are the most predominant Gram-negative bacteria (GNB) isolated among bloodstream infections (BSI). Additionally, the multidrug-resistant nature of these organisms is not only a threat to patients but it also poses a big public health challenge to current treatments and highlights the need for the development of new antimicrobials. Therefore, CRE have been placed on the critical priority list by the World Health Organization (WHO). We aimed to provide a holistic overview of the GERMS-SA CRE BSI surveillance data from 01 July 2015–31 December 2021.</p>



<p class="wp-block-paragraph"><strong>Authors</strong></p>



<p class="wp-block-paragraph"><a class="author-name" data-author-id="0">Husna Ismail, </a><a class="author-name" data-author-id="1">Thembekile Buhle Christna Zwane, </a><a class="author-name" data-author-id="2">Elloise Du Toit, </a><a class="author-name" data-author-id="3">Renata Maria Augusto da Costa, </a><a class="author-name" data-author-id="4">François Franceschi, </a><a class="author-name" data-author-id="5">Olga Perovic</a></p>



<p class="wp-block-paragraph">&nbsp;</p>



<p class="has-text-align-center wp-block-paragraph"><a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0324262">Read the publication</a></p>

<p><a href="https://gardp.org/carbapenem-resistant-enterobacterales-among-patients-with-bloodstream-infections-in-south-africa-consolidated-surveillance-data-2015-2021/">Source</a></p>]]></content:encoded>
					
		
		
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