Multiple-Ascending-Dose Phase 1 Clinical Study of the Safety, Tolerability, and Pharmacokinetics of CRS3123, a Narrow-Spectrum Agent with Minimal Disruption of Normal Gut Microbiota

Author:

Lomeli Barbara K.1,Galbraith Hal1,Schettler Jared1,Saviolakis George A.2,El-Amin Wael2,Osborn Blaire3,Ravel Jacques45ORCID,Hazleton Keith6,Lozupone Catherine A.7,Evans Ronald J.8,Bell Stacie J.8,Ochsner Urs A.8,Jarvis Thale C.8,Baqar Shahida3,Janjic Nebojsa8

Affiliation:

1. Quintiles Phase One Services, Overland Park, Kansas, USA

2. DynPort Vaccine Company LLC, Frederick, Maryland, USA

3. Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA

4. Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA

5. Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA

6. Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA

7. Division of Biomedical Informatics and Personalized Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA

8. Crestone, Inc., Boulder, Colorado, USA

Abstract

CRS3123 is a novel small molecule that potently inhibits methionyl-tRNA synthetase of Clostridioides difficile , inhibiting C. difficile toxin production and spore formation. CRS3123 has been evaluated in a multiple-ascending-dose placebo-controlled phase 1 trial.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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