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NCT Number: NCT06717594

PK/PD Relationship of CAZ/AVI and FOS in the Treatment of Patients With Infections Due to CRE

A multicenter international prospective observational pharmacological study in adult patients (≥18 years) treated with ceftazidime/avibactam (CAZ/AVI) alone or with CAZ/AVI plus fosfomycin (FOS) for infection due to carbapenem-resistant Enterobacterales (CRE) (KPC and/or OXA-48).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy

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About this study

Gram-negative infections, particularly those caused by carbapenem-resistant Enterobacterales (CRE), have a dramatic impact on patient survival. Despite the introduction of new drugs in the last years have improved the outcome of patients with CRE infections, mortality and relapse rates are still relevant, especially in patients with high-risk source as pneumonia, and those in which the attainment of optimal exposure could be reduced by underlying renal disease. The use of combination regimen in these scenarios has been proposed. However, a standardized approach is still missing. Since several in vitro studies have highlighted the synergistic effect of fosfomycin (FOS) with different antibiotic classes, including cephalosporins such drug could be an appealing option in combination therapy for the management of CRE infections.

In particular, the primary aim of the study is to assess the probability of achieving a pre-defined target of efficacy in patients treated with ceftazidime/avibactam (CAZ/AVI) and/or FOS according to different modes of drug administration in patients with CRE infections.

Secondary aim is to assess the association between plasma drug concentration of both CAZ/AVI and FOS and patient response.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signature of the informed consent
  • Age ≥ 18 years
  • Adult patients treated for ≥ 48 hours with CAZ/AVI or CAZ/AVI plus FOS for a microbiologically documented CRE infection

Exclusion criteria

  • Polymicrobial/mixed infections with exception of cases with multiple Enterobacterales susceptible to study drugs

Treatment and study plan

Primary outcomes

  1. PK/PD efficacy targets for study drugs

    Time frame: From enrollment (treatment onset) to 48 and 72 hours after starting treatment

    The primary endpoint will be the attainment of the pre-defined PK/PD target of efficacy at 48 and 72 hours after starting treatment for Carbapenem-resistant Enterobacterales (CRE) infection

Secondary outcomes

  1. Difference in SOFA score

    Time frame: From day 0 (day of index positive culture) and day 7

    Difference in SOFA score between day 0 (day of treatment onset) and day 7

  2. Trend of C-Reactive Protein (CRP) and Procalcitonin (PCT)

    Time frame: From day 0 (day of index positive culture) and day 7

    Trend of C-Reactive Protein (CRP) and Procalcitonin (PCT) from day 0 to day 7 after treatment onset

  3. Microbiological eradication

    Time frame: From day 0 (day of index positive culture) and day 7

    Microbiological eradication defined as bacteraemia clearance or negativization of index diagnostic sample within 7 days from treatment onset

  4. Relapse and/or reinfection

    Time frame: From enrollment to the end of the follow-up at three months

    Relapse (new infection with the same pathogen emerging after treatment) and/or reinfection (new infection with a different pathogen emerging after treatment) rates at day 90

  5. All-cause mortality

    Time frame: From enrollment to the end of the follow-up at three months

    All-cause mortality at day 30 and at day 90

Study contacts

Contact information is provided by the study sponsor or research team.

Maddalena Giannella, MD PhD

CONTACT

[email protected]

+390512143199

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Official study title

PK/PD Relationship of CAZ/AVI and FOS in the Treatment of Patients With Infections Due to Carbapenem-resistant Enterobacterales (CRE)

Acronym: CAVIFOS

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Dec 5, 2024
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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