A New “Non-Traditional” Antibacterial Drug Fluorothiazinone—Clinical Research in Patients with Complicated Urinary Tract Infections

Author:

Zigangirova Nailya A.1,Lubenec Nadezda L.1,Beloborodov Vladimir B.12,Sheremet Anna B.1ORCID,Nelyubina Stanislava A.1,Bondareva Nataliia E.1,Zakharov Konstantin A.3ORCID,Luyksaar Sergey I.1,Zolotov Sergey A.1,Levchenko Evgenia U.1,Luyksaar Svetlana V.1,Koroleva Ekaterina A.1,Fedina Elena D.1,Simakova Yana V.1ORCID,Pushkar Dmitry Yu.45,Gintzburg Alexander L.16

Affiliation:

1. National Research Center for Epidemiology and Microbiology named after the Honorary Academician N. F. Gamaleya, 18 Gamaleya St., 123098 Moscow, Russia

2. Medical Academy of Continuous Professional Education, 2/1 Barrikadnaya St., 125993 Moscow, Russia

3. Accellena LLC, 88, lit.A., Sredniy pr. V.O., 199106 St. Petersburg, Russia

4. Department of Urology Russian University of Medicine of the Ministry of Healthcare of the Russian Federation, 4 Dolgorukovskaya St., 127006 Moscow, Russia

5. S. P. Botkin City Clinical Hospital, Moscow Healthcare Department, 5/20 2nd Botkinsky Proezd, 125284 Moscow, Russia

6. Department of Infectious Diseases and Virology, First Moscow State Medical University named after I. M. Sechenov, Institute of Professional Education, 18 Gamaleya St., 123098 Moscow, Russia

Abstract

In order to combat resistance, it is necessary to develop antimicrobial agents that act differently from conventional antibiotics. Fluorothiazinone, 300 mg tablet (The Gamaleya National Research Center), is an original antibacterial drug based on a new small molecule T3SS and flagellum inhibitor. A total of 357 patients with complicated urinary tract infections (UTIs) were divided into two groups and given Fluorothiazinone 1200 mg/day or a placebo for 7 days to evaluate the efficacy and safety of the drug. Additionally, all patients were given Cefepime 2000 mg/day. Fluorothiazinone with Cefepime showed superiority over placebo/Cefepime based on the assessment of the proportion of patients with an overall outcome in the form of a cure after 21 days post-therapy (primary outcome), overall outcome in cure rates, clinical cure rates, and microbiological efficacy at the end of therapy and after 21 days post-therapy (secondary outcomes). In patients who received Fluorothiazinone, the rate of infection recurrences 53 and 83 days after the end of the therapy was lower by 18.9%, compared with patients who received placebo. Fluorothiazinone demonstrated a favorable safety profile with no serious unexpected adverse events reported. The results showed superiority of the therapy with Fluorothiazinone in combination with Cefepime compared with placebo/Cefepime in patients with cUTIs.

Funder

The Ministry of Health of the Russian Federation

Publisher

MDPI AG

Reference33 articles.

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