Aztreonam-avibactam for the treatment of serious infections caused by metallo-β-lactamase-producing Gram-negative pathogens: a Phase 3 randomized trial (ASSEMBLE)

dc.contributor.authorDaikos G.L.
dc.contributor.authorCisneros J.M.
dc.contributor.authorCarmeli Y.
dc.contributor.authorWang M.
dc.contributor.authorLeong C.L.
dc.contributor.authorPontikis K.
dc.contributor.authorAnderzhanova A.
dc.contributor.authorFlorescu S.
dc.contributor.authorKozlov R.
dc.contributor.authorRodriguez-Noriega E.
dc.contributor.authorPsichogiou M.
dc.contributor.authorRattanaumpawan P.
dc.contributor.authorStreinu-Cercel A.
dc.contributor.authorRamasubramanian V.
dc.contributor.authorArhin F.F.
dc.contributor.authorRogers H.
dc.contributor.authorWible M.
dc.contributor.authorLeaney J.
dc.contributor.authorJacobson D.
dc.contributor.authorPypstra R.
dc.contributor.authorChow J.W.
dc.contributor.correspondenceDaikos G.L.
dc.contributor.otherMahidol University
dc.date.accessioned2025-08-04T18:19:31Z
dc.date.available2025-08-04T18:19:31Z
dc.date.issued2025-08-01
dc.description.abstractBackground The Phase 3 ASSEMBLE study investigated aztreonam-avibactam versus best available therapy (BAT) for treatment of complicated intra-abdominal infection (cIAI), complicated urinary tract infection (cUTI), hospital-acquired/ventilator-associated pneumonia (HAP/VAP) or bloodstream infection (BSI) caused by confirmed MBL-producing multidrug-resistant pathogens. Methods This prospective, multicentre, randomized, open-label, central assessor-blinded study randomized hospitalized adults 2:1 to aztreonam-avibactam [+ metronidazole (cIAI)] or BAT for 5-14 (cIAI, cUTI and BSI) or 7-14 (HAP/VAP) days. Primary endpoint was clinical cure at test-of-cure (TOC) visit on Day 28  ±  3 [microbiological ITT (micro-ITT) analysis set]. Secondary endpoints included microbiological response at TOC, 28-day mortality and safety. No formal hypothesis testing was planned. Results Fifteen patients were randomized [aztreonam-avibactam, n = 12; BAT, n = 3 (ITT and micro-ITT analysis sets)]. Most frequent baseline pathogens were Enterobacterales; Klebsiella pneumoniae was most common [aztreonam-avibactam, 6/12 (50%); BAT, 2/3 (67%)]. MBL subtypes/variants identified in the aztreonam-avibactam group were NDM-1 (n = 7), NDM-5 (n = 3), VIM-2 (n = 2) and L1 (n = 3); and for BAT were NDM-1 (n = 2) and NDM-5 (n = 1). Clinical cure rates at TOC were 5/12 (42%) for aztreonam-avibactam and 0/3 (0%) for BAT. Per-patient microbiological responses were generally consistent with clinical responses. Twenty-eight-day all-cause mortality rates for aztreonam-avibactam and BAT were 1/12 (8%) and 1/3 (33%), respectively. Aztreonam-avibactam was generally well-tolerated, with no treatment-related serious adverse events. Conclusions These Phase 3 data provide support for aztreonam-avibactam as a potential therapeutic option for difficult-to-treat infections caused by MBL-producing Gram-negative bacteria.
dc.identifier.citationJac Antimicrobial Resistance Vol.7 No.4 (2025)
dc.identifier.doi10.1093/jacamr/dlaf131
dc.identifier.eissn26321823
dc.identifier.scopus2-s2.0-105011867129
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/111539
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.subjectImmunology and Microbiology
dc.titleAztreonam-avibactam for the treatment of serious infections caused by metallo-β-lactamase-producing Gram-negative pathogens: a Phase 3 randomized trial (ASSEMBLE)
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105011867129&origin=inward
oaire.citation.issue4
oaire.citation.titleJac Antimicrobial Resistance
oaire.citation.volume7
oairecerif.author.affiliationFudan University
oairecerif.author.affiliationNational and Kapodistrian University of Athens
oairecerif.author.affiliationPfizer Inc.
oairecerif.author.affiliationUniversitatea de Medicina si Farmacie Carol Davila din Bucuresti
oairecerif.author.affiliationTel Aviv Sourasky Medical Center
oairecerif.author.affiliationHospital Universitario Virgen del Rocío
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationPfizer Limited, UK
oairecerif.author.affiliationKuala Lumpur Hospital
oairecerif.author.affiliationKAT Hospital
oairecerif.author.affiliationHospital Civil de Guadalajara
oairecerif.author.affiliationVictor Babes National Institute
oairecerif.author.affiliationApollo Hospitals Group
oairecerif.author.affiliationSmolensk State Medical Academy
oairecerif.author.affiliationChest Diseases Hospital 'Sotiria'
oairecerif.author.affiliationInstitutul Naţional de Boli Infecţioase „Prof. Dr. Matei Balş“
oairecerif.author.affiliationNational Health Commission of the People's Republic of China
oairecerif.author.affiliationPfizer Inc.
oairecerif.author.affiliationSBHI of the City of Moscow 'N.I.Pirogov City Clinical Hospital #1'

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