drugset / Trial / NCT04209855

A Study of Mirvetuximab Soravtansine vs. Investigator's Choice (IC) of Chemotherapy in Platinum-Resistant, Advanced High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers With High Folate Receptor-Alpha (FRα) Expression

NCT04209855

RandomizedParallel-groupOpen-labelTreatment

Summary

This Phase 3 study is designed to compare the efficacy and safety of mirvetuximab soravtansine (MIRV) vs. IC chemotherapy in participants with platinum-resistant high-grade epithelial ovarian cancer, primary peritoneal, or fallopian tube cancer, whose tumors express a high-level of FRα. Participants will be, in the opinion of the Investigator, appropriate for single-agent therapy for their next line of therapy. The FRα positivity will be defined by the Ventana FOLR1 (FOLR1-2.1) CDx assay.

Timeline

Start
2019-12-31
Primary completion
2023-03-06
Completion
2024-10-29

Drugs

EvaluationDrugModalityDoseRoute
Comparator Doxorubicin Other / unclassified 40 mg/m2 Intravenous
Subject Mirvetuximab Soravtansine Other / unclassified 6 mg/kg Intravenous
Comparator Paclitaxel Small molecule 80 mg/m2 Intravenous
Comparator Topotecan Small molecule 1.25 mg/m2
Comparator Topotecan Small molecule 4 mg/m2