Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in Platinum-sensitive Epithelial Ovarian, Fallopian Tube, or Peritoneal Cancer

ID#: NCT05445778

Age: 18 years - 66+

Gender: Female

Healthy Subjects: No

Study Phase: Phase 3

Recruitment Status: Recruiting

Start Date: December 27, 2022

End Date: April 01, 2029

Contact Information:
ABBVIE CALL CENTER
844-663-3742
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:



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