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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, click the link below:

 

https://clinicaltrials.gov/study/NCT05445778?term=IMGN853-0421&rank=1

 

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