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Study identifier: NCT07478484 Synced from ClinicalTrials.gov · July 29, 2026
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Different Administration Regimens of CAZ-AVI in Combination With ATM for the Treatment of CR-GNB

Condition: Ceftazidime-avibactam · Aztreonam · Gram-negative Bacterial Infection  ·  Sponsor: Jing Zhou

PhasePhase 4
Planned participants144
Who can joinAll sexes, 18 Years to 100 Years
Healthy volunteersNo

About this study

Metallo-β-lactamase-producing carbapenem-resistant Gram-negative bacteria (MBL-CR-GNB), due to their capacity to hydrolyze almost all β-lactam antibiotics, have become a critical global threat in antimicrobial resistance. Current novel β-lactamase inhibitors (e.g., avibactam, relebactam, vaborbactam) only inhibit serine enzymes and are ineffective against metallo-β-lactamases (MBL), severely limiting clinical treatment options. Aztreonam (ATM) is inherently stable against MBL, while avibactam (AVI) inhibits co-produced serine β-lactamases (e.g., KPC, OXA-48). Their combination achieves complementary synergistic antibacterial effects. The ceftazidime-avibactam plus aztreonam (CZA+ATM) regimen, operating via the mechanism of "avibactam protecting aztreonam", has demonstrated synergistic bactericidal activity against NDM, VIM, IMP and other MBL-producers in multiple real-world and clinical studies, significantly reducing infection-related mortality.However, although current domestic and international guidelines recommend the CZA+ATM combination for MBL infections, there is no consensus on optimal infusion strategies. Based on the above, this study hypothesizes that in patients with complicated infections caused by MBL-producing CR-GNB, different infusion modalities of ceftazidime-avibactam combined with aztreonam-concomitant infusion versus sequential infusion-will show no significant differences in PK/PD target attainment rates, clinical cure rates, microbiological eradication …

This description comes directly from the study's public registry record.

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Locations (1)

Jing ZhouNanjin, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07478484