Last updated on March 2020

Study to Assess Safety Tolerability and Efficacy of Incremental Doses of MGB-BP-3 in Patients With CDAD


Brief description of study

The objective of this Phase IIa study is to assess the safety, tolerability, and efficacy of incremental doses of MGB-BP-3 in patients with Clostridium difficile-associated diarrhea (CDAD).

Detailed Study Description

This is an exploratory, Phase IIa, open-label study assessing the safety, tolerability, and efficacy of incremental doses of MGB-BP-3 with 3 sequential groups of 10 patients with CDAD. Patients will be administered an oral dose of MGB-BP-3 for 10 days (Day 1 to Day 10). At the end of the treatment period, patients will be followed for up to 8 weeks to assess the incidence of disease recurrence.

Clinical Study Identifier: NCT03824795

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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