drugset / Trial / NCT00468728

PAR-101/OPT-80 Versus Vancomycin for the Treatment of Clostridium Difficile-Associated Diarrhea (CDAD)

NCT00468728 ↗

Phase 3 Completed 535 enrolled Optimer Pharmaceuticals LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a comparative study to investigate the safety and efficacy of PAR-101/OPT-80 (fidaxomicin) versus vancomycin in subjects with Clostridium difficile-associated diarrhea (CDAD).

Timeline

Start
2006-10-04
Primary completion
2009-12-11
Completion
2009-12-11

Outcome

Met primary endpoint

paper 198 (91·7%) of 216 patients in the per-protocol population given fidaxomicin achieved clinical cure, compared with 213 (90·6%) of 235 given vancomycin, meeting the criterion for non-inferiority (one-sided 97·5% CI -4·3%). PMID 22321770 ↗

paper Non-inferiority was also shown for clinical cure in the mITT population PMID 22321770 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Fidaxomicin Other / unclassified 200 mg Oral
Comparator Vancomycin Other / unclassified 125 mg Oral