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Novel antibiotics in development to treat Clostridium difficile infection
- Source :
- Current Opinion in Gastroenterology. 33:1-7
- Publication Year :
- 2017
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2017.
-
Abstract
- PURPOSE OF REVIEW Clostridium difficile infections (CDI) remain a challenge to treat clinically due primarily to limited number of antibiotics available and unacceptably high recurrence rates. Because of this, there has been significant demand for creating innovative therapeutics, which has resulted in the development of several novel antibiotics. RECENT FINDINGS This review updates seven different antibiotics that are currently in development to treat CDI including fidaxomicin, surotomycin, ridinilazole, ramoplanin, cadazolid, LFF571, and CRS3123. Available preclinical and clinical data are compared between these antibiotics. SUMMARY Many of these new antibiotics display almost ideal properties for antibiotics directed against CDI. Despite these properties, not all clinical development of these compounds has been successful. These studies have provided key insights into the pathogenesis of CDI and will continue to inform future drug development. Successful phase III clinical trials should result in several new and novel antibiotics to treat CDI.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
genetic structures
Pyridines
medicine.drug_class
030106 microbiology
Antibiotics
Surotomycin
Thiophenes
Peptides, Cyclic
Lipopeptides
03 medical and health sciences
chemistry.chemical_compound
Depsipeptides
medicine
Humans
Benzopyrans
Fidaxomicin
Intensive care medicine
Oxazolidinones
Clinical Trials as Topic
business.industry
Gastroenterology
Ramoplanin
Clostridium difficile
Clostridium difficile infections
Anti-Bacterial Agents
Thiazoles
Drug development
chemistry
Clostridium Infections
Benzimidazoles
business
Cadazolid
medicine.drug
Subjects
Details
- ISSN :
- 02671379
- Volume :
- 33
- Database :
- OpenAIRE
- Journal :
- Current Opinion in Gastroenterology
- Accession number :
- edsair.doi.dedup.....525a377a22c51eaec2d9788ffc575250
- Full Text :
- https://doi.org/10.1097/mog.0000000000000332