drugset / Trial / NCT02917200

Safety and Efficacy Study of Different DAV132 Dose Regimens in Healthy Volunteers

NCT02917200 ↗

Phase 1 Completed 150 enrolled Da Volterra
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate whether different DAV132 dose regimens are safe and effective for capturing fecal residues of moxifloxacin in healthy volunteers.

Timeline

Start
2016-05-11
Primary completion
2016-12-02
Completion
2016-12-02

Drugs

EvaluationDrugModalityDoseRoute
Background Moxifloxacin Small molecule 400 mg Oral

Indications

No indication recorded.