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.author | Daikos G.L. | |
| dc.contributor.author | Cisneros J.M. | |
| dc.contributor.author | Carmeli Y. | |
| dc.contributor.author | Wang M. | |
| dc.contributor.author | Leong C.L. | |
| dc.contributor.author | Pontikis K. | |
| dc.contributor.author | Anderzhanova A. | |
| dc.contributor.author | Florescu S. | |
| dc.contributor.author | Kozlov R. | |
| dc.contributor.author | Rodriguez-Noriega E. | |
| dc.contributor.author | Psichogiou M. | |
| dc.contributor.author | Rattanaumpawan P. | |
| dc.contributor.author | Streinu-Cercel A. | |
| dc.contributor.author | Ramasubramanian V. | |
| dc.contributor.author | Arhin F.F. | |
| dc.contributor.author | Rogers H. | |
| dc.contributor.author | Wible M. | |
| dc.contributor.author | Leaney J. | |
| dc.contributor.author | Jacobson D. | |
| dc.contributor.author | Pypstra R. | |
| dc.contributor.author | Chow J.W. | |
| dc.contributor.correspondence | Daikos G.L. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2025-08-04T18:19:31Z | |
| dc.date.available | 2025-08-04T18:19:31Z | |
| dc.date.issued | 2025-08-01 | |
| dc.description.abstract | Background 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.citation | Jac Antimicrobial Resistance Vol.7 No.4 (2025) | |
| dc.identifier.doi | 10.1093/jacamr/dlaf131 | |
| dc.identifier.eissn | 26321823 | |
| dc.identifier.scopus | 2-s2.0-105011867129 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/111539 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Medicine | |
| dc.subject | Immunology and Microbiology | |
| dc.title | Aztreonam-avibactam for the treatment of serious infections caused by metallo-β-lactamase-producing Gram-negative pathogens: a Phase 3 randomized trial (ASSEMBLE) | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105011867129&origin=inward | |
| oaire.citation.issue | 4 | |
| oaire.citation.title | Jac Antimicrobial Resistance | |
| oaire.citation.volume | 7 | |
| oairecerif.author.affiliation | Fudan University | |
| oairecerif.author.affiliation | National and Kapodistrian University of Athens | |
| oairecerif.author.affiliation | Pfizer Inc. | |
| oairecerif.author.affiliation | Universitatea de Medicina si Farmacie Carol Davila din Bucuresti | |
| oairecerif.author.affiliation | Tel Aviv Sourasky Medical Center | |
| oairecerif.author.affiliation | Hospital Universitario Virgen del Rocío | |
| oairecerif.author.affiliation | Siriraj Hospital | |
| oairecerif.author.affiliation | Pfizer Limited, UK | |
| oairecerif.author.affiliation | Kuala Lumpur Hospital | |
| oairecerif.author.affiliation | KAT Hospital | |
| oairecerif.author.affiliation | Hospital Civil de Guadalajara | |
| oairecerif.author.affiliation | Victor Babes National Institute | |
| oairecerif.author.affiliation | Apollo Hospitals Group | |
| oairecerif.author.affiliation | Smolensk State Medical Academy | |
| oairecerif.author.affiliation | Chest Diseases Hospital 'Sotiria' | |
| oairecerif.author.affiliation | Institutul Naţional de Boli Infecţioase „Prof. Dr. Matei Balş“ | |
| oairecerif.author.affiliation | National Health Commission of the People's Republic of China | |
| oairecerif.author.affiliation | Pfizer Inc. | |
| oairecerif.author.affiliation | SBHI of the City of Moscow 'N.I.Pirogov City Clinical Hospital #1' |
