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Early-stage Ovarian Clear Cell Carcinoma (OCCC) Patients at Risk of Recurrence

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National Taiwan University

Status

Not yet enrolling

Conditions

FIGO Stage IC2 to II Ovarian Clear Cell Carcinoma

Study type

Observational

Funder types

Other

Identifiers

NCT06237946
202310152RIND

Details and patient eligibility

About

The goal of this observational study is to determine the risk of recurrence in early-stage OCCC (Ovarian Clear Cell Carcinoma) patients who received postoperative adjuvant treatment.

Participants were received platinum-based adjuvant therapy following debulking surgery will be included for the study.

Full description

This is a retrospective, global multicenter, single-arm, study for early-stage OCCC (Ovarian Clear Cell Carcinoma) patients at risk of recurrence following the first-line treatment. This study is planned to enroll 272 patients eligible for participation from two study sites in Taiwan, one in Korea, and one in Japan. The study will use archival Formalin-Fixed Paraffin-Embedded (FFPE) samples from patients who have received adjuvant therapy following debulking surgery. The study is designed to identify OCCC patients at risk for relapse and apply clinical stratification by IHC staining of 3 selected markers (CD45, CD8, tryptase) to prepare as clinical assays.

Enrollment

272 estimated patients

Sex

Female

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women aged ≥20 years old.
  • Participant with histologically confirmed OCCC of stage IC2, IC3, IIA and IIB by International Federation of Gynecology and Obstetrics (FIGO) 2014 system.
  • Participant has received platinum-based regimens for 3 to 6 cycles combined with paclitaxel, gemcitabine, cyclophosphamide, or bevacizumab adjuvant therapy following debulking surgery.
  • Formalin-fixed paraffin-embedded (FFPE) tissue samples available.

Exclusion criteria

  • Absence of histological confirmation of the diagnosis.
  • Unusable sample or biologically deteriorated.

Trial contacts and locations

0

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Central trial contact

Ling-Hung Wei

Data sourced from clinicaltrials.gov

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