Results 91 to 100 of about 4,025 (198)

Partial Courses of Fidaxomicin Followed by Oral Vancomycin and the Effect on Recurrence of Clostridioides difficile Infections [PDF]

open access: yes
BACKGROUND: Clostridioides difficile infection (CDI) causes a significant national health care burden. Literature has demonstrated lower rates of CDI recurrence with fidaxomicin compared with oral vancomycin.
Ahmad, Zayd   +6 more
core   +3 more sources

Comparative Susceptibilities to Fidaxomicin (OPT-80) of Isolates Collected at Baseline, Recurrence, and Failure from Patients in Two Phase III Trials of Fidaxomicin against Clostridium difficile Infection

open access: yes, 2011
A 10-day course of oral fidaxomicin (200 mg twice a day [b.i.d.]), a potent new macrocyclic drug, was compared to vancomycin (125 mg four times a day [q.i.d.]) in 1,164 adults (1,105 in the modified intent-to-treat [mITT] population) with ...
Ellie J. C. Goldstein   +5 more
core   +1 more source

Improving fidaxomicin production through ARTP mutagenesis and fermentation optimization in Actinoplanes deccanensis

open access: yesSynthetic and Systems Biotechnology
Fidaxomicin, a macrolide antibiotic, is widely used to treat Clostridioides difficile infection (CDI). It demonstrats significantly higher clinical efficacy than vancomycin and metronidazole. However, the large-scale industrial production of it remains a
Jing-Yi Ruan   +6 more
doaj   +1 more source

The environmental stress σ subunits render M. tuberculosis RNA polymerase resistant to fidaxomicin by restricting its binding pocket conformational plasticity

open access: yes
Fidaxomicin is a narrow-spectrum antibiotic that inhibits bacterial RNA polymerase (RNAP) at an early stage of transcription initiation. Fidaxomicin is used for treating Clostridioides difficile infections and has demonstrated in vitro efficacy against ...
Laurent Chaloin   +5 more
core   +1 more source

SARS‐CoV‐2 PLpro Inhibition: Evaluating in Silico Repurposed Fidaxomicin's Antiviral Activity Through In Vitro Assessment

open access: yesChemistryOpen
The emergence of drug‐resistant viruses and novel strains necessitates the rapid development of novel antiviral therapies. This need was particularly demanding during the COVID‐19 pandemic.
B.Sc. Sara Protić   +10 more
doaj   +1 more source

Evaluating Bezlotoxumab-Fidaxomicin Combination Therapy in Clostridioides Infection: A Single-Center Retrospective Study from Aichi Prefecture, Japan

open access: yesAntibiotics
Background/Objectives: Clostridioides difficile infection (CDI) poses a significant healthcare challenge, with recurrence rates reaching 30%, leading to substantial morbidity and costs.
Jun Hirai   +5 more
doaj   +1 more source

Treatment of pediatric Clostridium difficile infection: a review on treatment efficacy and economic value

open access: yesInfection and Drug Resistance, 2017
Amanda R D’Ostroph,1 Tsz-Yin So2 1UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, 2Department of Pharmacy, Moses H Cone Memorial Hospital, Greensboro, NC, USA Abstract: The incidence of Clostridium ...
D'Ostroph AR, So TY
doaj  

A Review of Therapies for Clostridioides difficile Infection

open access: yesAntibiotics
Clostridioides difficile is an urgent public health threat that affects approximately half a million patients annually in the United States. Despite concerted efforts aimed at the prevention of Clostridioides difficile infection (CDI), it remains a ...
Faiza Morado, Neha Nanda
doaj   +1 more source

Antimicrobial Susceptibility of Clostridioides difficile in Spain: Multicenter Retrospective Cohort Study

open access: yesAntibiotics
Background/Objetives: The objective of this study was to determine the in vitro susceptibility profiles of clinical Clostridioides difficile isolates to metronidazole (MTZ), vancomycin (VAN), fidaxomicin (FDX), tigecycline (TGC), and eravacycline (ERV ...
María-Paz Ventero   +17 more
doaj   +1 more source

Reshaping Natural Products: New Fidaxomicin Antibiotics and Darobactin-Like Peptides

open access: yes
This thesis is structured into two chapters which detail different approaches for the optimisation and mimicry of natural products. The first chapter covers the development of new antibiotic derivatives based on the natural product fidaxomicin.
Jung, Erik
core  

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