Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

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 typeObservational
Ages18 Years and up
SexWomen only
Enrollment500 (estimated)
SponsorAbbVie
Industry-sponsored
Drugs / interventionsmirvetuximab
Locations1 site (Vienna)
StatusRecruiting
StartedOctober 21, 2026
Main results expectedApril 2030
Study endsApril 2030
Registry record updatedOctober 27, 2026
Trial IDNCT07896421 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

  • Medizinische Universitaet Wien /ID# 282657
    Vienna, Austria
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.