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Safety and Efficacy of DAV132 in Patients at High-Risk for Clostridium Difficile Infection (CDI) — SHIELD  

Clostridium Difficile Infection Clinical Trial

Official title:
A European Multicenter, Randomized, Parallel-group Study to Evaluate the Safety and Efficacy/Performance of DAV132 in Hospitalized Patients at High Risk for Clostridium Difficile Infection and Who Receive Fluoroquinolones for the Treatment of Acute Infections

Clinical Trial Summary

The purpose of this study is to determine the safe use and evaluate the efficacy/performance of DAV132 in hospitalized patients at high risk for Clostridium difficile infection (CDI) and who receive fluoroquinolones (FQs) for the treatment of acute infections or for prophylaxis of febrile neutropenia.

Clinical Trial Description

Da Volterra develops DAV132, a novel therapeutic option preserving the intestinal microbiota, to prevent potentially life-threatening conditions such as CDI or emergence of antibiotic-resistant bacteria. Prevention of CDI remains critical unmet need, especially for patients at high risk of developing such infection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03710694
Study type Interventional
Source Da Volterra
Contact
Status Completed
Phase N/A
Start date October 31, 2018
Completion date August 9, 2019
View Details
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