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GOG-3078/IMGN853-0421 GLORIOSA

Trial Overview

Official Title

Randomized, multicenter, open-label, Phase 3 study of mirvetuximab soravtansine in combination with bevacizumab versus bevacizumab alone as maintenance therapy for patients with FR alpha-high recurrent platinum-sensitive epithelial ovarian, fallopian tube, or primary peritoneal cancers who have not progressed after second-line platinum-based chemotherapy plus bevacizumab (GLORIOSA)

Study Purpose

To compare progression-free survival after platinum-based chemotherapy (doublet) plus bevacizumab and randomized to maintenance mirvetuxemab sorvtansine (MIRV) plus bevacizumab (Arm 1) versus bevacizumab alone (Arm 2)

Diagnosis

High-grade serous ovarian, primary peritoneal, or fallopian tube cancer.

Eligibility

Platinum-sensitive. 1 prior line of therapy. FR alpha high (>/= 75%). Tumor tissue testing required.

 

Intervention

Maintenance mirvetuxemab sorvtansine (MIRV) plus bevacizumab (Arm 1) versus bevacizumab alone (Arm 2)

For more information visit Clinicaltrials.gov

Key Participation Requirements
Gender
Female
Age
19 years of age or older
Enrollment Status
Recruiting
Phase
Phase III
Methodist Health System Trial Code
GOG-3078/IMGN853-0421