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Study identifier: NCT06966284 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Post-Marketing Study to Assess the Efficacy and Safety of Intravenous Polymyxin B and Colistin Methanesulfonate in Patients With Carbapenem-Resistant Gram-Negative Bacterial Infection

Condition: Bacteremia Caused by Gram-Negative Bacteria · Bacterial Pneumonia  ·  Sponsor: TTY Biopharm

PhaseN/A
Planned participants480
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a retrospective, observational, post-marketing study to evaluate the clinical response, microbiological response, mortality, and safety of intravenous polymyxin B and colistin methanesulfonate in patients with carbapenem-resistant gram-negative bacterial infection. Subgroup analysis by sites of infection, infectious pathogens, and baseline renal function will also be performed.

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

Talk to the study team

Angel Chen  ·  886 2 26525999  ·  angel_chen@tty.com.tw

Always discuss trial participation with your own doctor first.

Locations (1)

Tri-Service General HospitalTaipei, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT06966284