Real-world use of mirvetuximab soravtansine in FRα-positive platinum-resistant ovarian, fallopian tube, and peritoneal cancer
Official title: Multi-country Real-World Observational Study of MIrvetuximab Soravtansine in Treating Platinum-REsistant FRALphA Positive Ovarian, Fallopian Tube, and Peritoneal Cancer- MIRELA
Run by AbbVie · NCT07896421 · Data updated 2026-11-12
This study tests how mirvetuximab soravtansine works in real-world adults with FRα-positive platinum-resistant ovarian, fallopian tube, or peritoneal cancer.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 500 (estimated) |
| Sponsor | AbbVie Industry-sponsored |
| Drugs / interventions | mirvetuximab |
| Locations | 1 site (Vienna) |
| Status | Recruiting |
| Started | October 21, 2026 |
| Main results expected | April 2030 |
| Study ends | April 2030 |
| Registry record updated | October 27, 2026 |
| Trial ID | NCT07896421 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with FRα-positive platinum-resistant ovarian, fallopian tube, or peritoneal cancer who are scheduled to receive mirvetuximab soravtansine monotherapy after 1-3 prior treatments.
✕Probably not a fit
Patients who do not receive MIRV monotherapy or have contraindications may not experience benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a global observational study enrolling about 500 adults who have FRα-positive platinum-resistant cancer and are to receive mirvetuximab soravtansine as monotherapy. Researchers will collect real-world data on treatment patterns, effectiveness, patient characteristics, biomarker testing, and health-related quality of life. The study will track outcomes as patients receive MIRV within the approved local labeling and standard care. Participation requires informed consent and patient-reported outcome data collection. No interventional procedures beyond routine treatment are involved.
Why it matters
Potential benefit: If successful, the study could provide real-world insights into how MIRV performs outside of trials and help guide future treatment decisions.
How similar studies have gone: Other observational data have shown real-world use of similar targeted therapies can inform practice, but this study focuses on MIRV in FRα-positive platinum-resistant disease and adds real-world context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants scheduled to be treated with mirvetuximab soravtansine in accordance with the local label, with treatment decision made independently before study enrollment * Signed informed consent and willingness to comply with study requirements including patient-reported outcome data collection Exclusion Criteria: * Any condition included in the contraindications section of the approved local mirvetuximab soravtansine label * Participation in a concurrent interventional clinical trial from enrollment throughout the study * Unwillingness or inability to comply with study requirements
Where it's running
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Medizinische Universitaet Wien /ID# 282657
Vienna, Austria Recruiting
Study contacts
- Study coordinator: Farah Khallaf
- Email: farah.khallaf@abbvie.com
- Phone: +1 (630) 2636202
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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AZD5335 versus mirvetuximab or chemotherapy for FRα-high and FRα-low platinum-resistant ovarian, fallopian tube, or peritoneal cancer
This will test whether AZD5335 works better than mirvetuximab for FRα-high tumors or better than single-agent chemotherapy for FRα-low tumors in women with high-grade, platinum-resistant ovarian, fallopian tube, or primary peritoneal cancer.
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Sofetabart Mipitecan (LY4170156) versus standard chemotherapy for platinum-resistant and platinum-sensitive high-grade ovarian, fallopian tube, and primary peritoneal cancer
This trial tests whether the targeted drug Sofetabart Mipitecan can better shrink tumors or delay progression than standard chemotherapies for people with platinum-resistant or platinum-sensitive high-grade ovarian, fallopian tube, or primary peritoneal cancer.
-
Mirvetuximab soravtansine combined with bevacizumab or carboplatin for FRα‑positive ovarian cancer
This Phase 2 trial tests whether giving intravenous mirvetuximab soravtansine with bevacizumab or carboplatin is safe and can change disease activity in adults with folate receptor alpha (FRα)–positive high‑grade ovarian, fallopian tube, or primary peritoneal cancer.
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Combining carboplatin with mirvetuximab soravtansine before surgery for FRα-positive advanced serous ovarian, fallopian tube, or primary peritoneal cancer
This will test whether giving mirvetuximab soravtansine with carboplatin before surgery helps people with newly diagnosed FRα-positive advanced-stage serous ovarian, fallopian tube, or primary peritoneal cancer.
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Mirvetuximab soravtansine for platinum-resistant high-grade ovarian, fallopian tube, and primary peritoneal cancer with high folate receptor-alpha
This trial tests whether intravenous mirvetuximab soravtansine helps people with platinum-resistant high-grade ovarian, fallopian tube, or primary peritoneal cancer whose tumors have high folate receptor-alpha.
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Carboplatin and Mirvetuximab for Advanced Ovarian Cancer Treatment
This study is testing if a combination of carboplatin and mirvetuximab can help women with advanced ovarian cancer do better after their initial chemotherapy before surgery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.