Treatment for Clostridium-difficile Infection With IMM529

Status Terminated

Clinical Trial Summary

This study will evaluate the safety and tolerability of IMM-529 together with standard of care (SOC) in patients with Clostridium-difficile Infection.

Clinical Trial Description

Subjects who provide voluntary written informed consent will be screened for eligibility. Subjects meeting all of the inclusion and none of the exclusion criteria will be eligible to participate.

Eligible subjects will be randomized up to 3 weeks post diagnosis of Clostridium-difficile Infection given SOC initiated already.

Each subject will return to the study clinic for assessment and required study procedures on Day 7, Day 14, Week 4, Week 8 and Week 12 post randomization. Treatment duration will be 28 days and follow up will last up to 12 weeks post randomization. ;

Study Design

Related Conditions & MeSH terms

Clostridium Difficile Infection
Clostridium Difficile Infection Recurrence
Clostridium Infections
Communicable Diseases
Infection
Recurrence

Clinical Trial Details

NCT number	NCT03065374
Study type	Interventional
Source	Immuron Ltd.
Contact
Status	Terminated
Phase	Phase 1/Phase 2
Start date	September 1, 2017
Completion date	November 7, 2019

View Details

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