drugset / Trial / NCT03667690

Study of Rezafungin Compared to Caspofungin in Subjects With Candidemia and/or Invasive Candidiasis

NCT03667690 ↗

Phase 3 Completed 199 enrolled Cidara Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this pivotal study is to determine if intravenous Rezafungin is efficacious and safe in the treatment of candidemia and/or invasive candidiasis when compared to caspofungin (followed by optional oral fluconazole).

Timeline

Start
2018-10-07
Primary completion
2021-10-07
Completion
2021-10-07

Outcome

Met primary endpoint

paper INTERPRETATION: Our data show that rezafungin was non-inferior to caspofungin for the primary endpoints of day-14 global cure (EMA) and 30-day all-cause mortality (FDA). PMID 36442484 ↗

release “ReSTORE trial met both primary endpoints and demonstrated non-inferiority of rezafungin versus current standard of care, caspofungin” mundipharma.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Caspofungin Other / unclassified 50 mg Intravenous
Subject Rezafungin Other / unclassified 200 mg Intravenous
Comparator Fluconazole Small molecule 6 mg/kg Oral

Indications