RecruitingNCT07539844

Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female Participants With Ovarian Cancer in Intercontinental (InterCon) Countries

A Concordance Study of Folate Receptor Alpha (FRa) Testing in InterCon Countries


Sponsor

AbbVie

Enrollment

1,000 participants

Start Date

Jul 2, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

Epithelial ovarian cancer (OC), including fallopian tube and primary peritoneal cancer, is the deadliest gynecologic malignant neoplasm with a 5-year relative survival of approximately 50%. This study will evaluate the concordance in folate receptor alpha (FRa) immunohistochemistry (IHC) in adult female participants with ovarian cancer. Archived tissue biopsies will be tested for FRa and data from approximately 1,000 participants will be collected. This is a retrospective study and testing will be performed prospectively on archived samples. Participants' charts will be reviewed. No drug will be administered as a part of this study. The duration of the study will be approximately 1 Year. There is no additional burden for participants in this trial.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with ovarian cancer. The study is currently recruiting participants at 5 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(5)

Instituto Alexander Fleming /ID# 281479

Ciudad Autonoma de Buenos Aire, Buenos Aires F.D., Argentina

Biomakers /ID# 280318

Buenos Aires, Argentina

Hospital Italiano de Buenos Aires /ID# 280315

Buenos Aires, Argentina

A.C. Camargo Cancer Center - Rua Professor Antonio Prudente /ID# 280407

São Paulo, Brazil

Fundacion Para La Investigacion Clinica Y Molecular Aplicada Del Cancer - Ficmac /ID# 282327

Bogotá, Bogota D.C., Colombia

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NCT07539844


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