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Clinical Trial Summary

The purpose of this research is to evaluate the primary objectives of safety and efficacy (rate of clinical cure) of 2 dosages of CRS3123 (200 mg and 400 mg) administered orally (po) twice daily (bid) and vancomycin administered 125 mg PO 4 times daily (qid) in adults > or equal to 18 years of age with a primary episode or first recurrence of CDI. The study will investigate the plasma concentrations and HRQoL outcomes of CRS3123 and additional efficacy endpoints as secondary objectives.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04781387
Study type Interventional
Source Crestone, Inc
Contact
Status Active, not recruiting
Phase Phase 2
Start date January 5, 2021
Completion date April 2024

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