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Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in Platinum-sensitive Epithelial Ovarian, Fallopian Tube, or Peritoneal Cancer
NOT_RECRUITINGPhase 3Sponsored by AbbVie
No longer actively recruiting
PhasePhase 3
SponsorAbbVie
Started2023-03-15
Est. completion2027-04
Eligibility
Age18 Years+
SexFEMALE
Healthy vol.Accepted
Locations74 sites
View on ClinicalTrials.gov →
NCT05445778
Summary
GLORIOSA is a Phase 3 multicenter, open label study designed to evaluate the safety and efficacy of mirvetuximab Soravtansine + Bevacizumab as maintenance therapy in participants with platinum-sensitive ovarian, primary peritoneal or fallopian tube cancers with high folate receptor-alpha (FRα) expression.
Eligibility
Age: 18 Years+Sex: FEMALEHealthy volunteers accepted
Inclusion Criteria: 1. Adult women \>/=18 years old 2. Confirmed diagnosis of high-grade serous epithelial ovarian, primary peritoneal, or fallopian tube cancer 3. Confirmed high FRα expression by regulatory-agency approved Ventana FOLR1 (FOLR1-2.1) 4. Relapsed disease after frontline (first-line) platinum-based chemotherapy and must be plantinum-sensitive 5. Willing and able to sign the informed consent form (ICF) and adhere to protocol requirements 6. Negative pregnancy test and willing to use highly effective contraceptive method(s) while on study medication and for at least 7 months after the last dose of MIRV and 6 months after the last dose of bevacizumab Exclusion Criteria: 1. Endometrioid, clear cell, mucinous, or sarconmatous histology; mixed tumors containing any of the above or low grade/borderline ovarian tumor 2. More than one line of prior chemotherapy before current/planned triplet therapy 3. PD (progressive disease) while on or following platinum-based therapy 4. Prior or whole-pelvis or wide-field radiotherapy 5. \> Grade 1 peripheral neuropathy 6. History of or concurrent ocular disorders 7. Grade 4 thromboembolic events 8. Not appropriate for bevacizumab treatment 9. Requiring use of folate-containing supplements 10. Prior hypersensitivity to monoclonal antibodies 11. Pregnant or breatfeeding women 12. Received prior MIRV or other FRα-targeting agents 13. Untreated or symptomatic central nervous system metastases 14. History of other malignancy within 3 years prior to signing study consent
Conditions4
CancerFallopian Tube CancerOvarian CancerPeritoneal Cancer
Interventions2
Locations74 sites
Usa Mitchell Cancer Institute /ID# 269661
Mobile, Alabama, 36604
City of Hope - Orange County Lennar Foundation Cancer Center /ID# 269573
Moores Cancer Center at UC San Diego /ID# 269564
Kaiser Permanente - Los Angeles Medical Center /ID# 269541
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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No longer actively recruiting
PhasePhase 3
SponsorAbbVie
Started2023-03-15
Est. completion2027-04
Eligibility
Age18 Years+
SexFEMALE
Healthy vol.Accepted
Locations74 sites
View on ClinicalTrials.gov →
NCT05445778