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

Recruiting Observational Study
Bacteremia Caused by Gram-Negative Bacteria Bacterial Pneumonia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
480 (estimated)
Sponsor
TTY Biopharm · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patient ≥ 18 years of age. 2. Patient diagnosed with bacterial pneumonia and/or bacteremia, or other physician judged serious infection (except urinary tract infection, UTI) caused by Carbapenem-Resistant Gram-Negative Bacteria (CR-GNB). CR-GNB: Resistant to at least one …
Contacts

Angel Chen

886 2 26525999

angel_chen@tty.com.tw

CONTACT