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Clinical trial

REFRaME-O1: A Phase 2/3 Open-label Study Evaluating the Efficacy and Safety of Luveltamab Tazevibulin (STRO-002) Versus Investigator's Choice (IC) Chemotherapy in Women With Relapsed Platinum-resistant Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers) Expressing Folate Receptor Alpha (FOLR1)

NCT05870748 is registered in ClinicalTrials.gov with Sutro Biopharma, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
REFRaME-O1: A Phase 2/3 Open-label Study Evaluating the Efficacy and Safety of Luveltamab Tazevibulin (STRO-002) Versus Investigator's Choice (IC) Chemotherapy in Women With Relapsed Platinum-resistant Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers) Expressing Folate Receptor Alpha (FOLR1)
Lead sponsor
Sutro Biopharma, Inc.
Phase
Phase 2/3
Overall status
Terminated
Start date
July 12, 2023
Completion date
August 26, 2025
Enrollment
600 (actual)
Sites
63

Conditions

As the registry lists them; a condition with its own page is linked.

epithelial ovarian cancer, fallopian tube cancer, ovarian cancer, platinum-resistant ovarian cancer, primary peritoneal cancer