drugset / Trial / NCT03824795

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

NCT03824795 ↗

Phase 2 Completed 34 enrolled MGB Biopharma Limited Syneos Health · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

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).

Timeline

Start
2019-02-07
Primary completion
2020-04-03
Completion
2020-04-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator MGB-BP-3 Small molecule 125 mg Oral
Comparator MGB-BP-3 Small molecule 250 mg Oral
Comparator MGB-BP-3 Small molecule 500 mg Oral