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NCT07407062Recruiting

A Study to Evaluate Folate Receptor Alpha (FRα) Expression in Adult Participants With Ovarian, Fallopian Tube, and Primary Peritoneal Cancer in Italy

Folate Receptor Alpha Expression in Relapsed Ovarian, Fallopian Tube and Primary Peritoneal Cancer: a Realworld prEvalence Study in Italy

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate the prevalence of folate receptor alpha (FRα)-positive status (≥75% viable tumor cells with moderate (2+) and/or strong (3+) membrane staining) in participants with high-grade serous ovarian, fallopian tube, and primary peritoneal cancer, stratified by time of sampling (initial diagnosis versus relapse), adhering to Ventana folate receptor alpha (FOLR1) RxDx (prescription diagnosis) assay Interpretation Guidance.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
6 Feb 2026
Start date
26 Jun 2026
Primary completion date
Nov 2026
Lead sponsor
AbbVie
NCT number
NCT07407062

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 26 Jun 2026 to the primary completion date, Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Diagnosis based on cytology and without any biopsy or surgical specimen

Other illness

  • Other histotypes than high grade serous ovarian cancer, fallopian tube cancer and primary peritoneal cancer

Other

  • Histological ambiguous diagnosis upon review
  • Archival or recurrent sample for the same participant not available

Who the study is looking for

  • Relapsed ovarian, fallopian tube and primary peritoneal cancer
  • Histologically high-grade serous carcinoma
  • Presence of archived surgical tissue samples from participants with epithelial ovarian cancer at diagnosis and at 1st recurrence in the same participants
  • Available samples collected from January 1st, 2016 to study start date (defined as study site initiation visit date) that are considered adequate for the Ventana folate receptor alpha (FOLR1) RxDx assay by the site pathologist

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Universita Cattolica /ID# 280205
Coordinator of this site? Confirm its status
RomeItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.