ClinicalTrials.Veeva

Menu

Real World Data Analysis of PARP Inhibitors Use in Patients With Ovarian Cancer

H

Hellenic Cooperative Oncology Group

Status

Active, not recruiting

Conditions

Ovarian Cancer

Treatments

Drug: PARP inhibitor

Study type

Observational

Funder types

Other

Identifiers

NCT04724031
P420_PARP

Details and patient eligibility

About

Real-world clinical outcomes and toxicity data will be evaluated in patients with advanced high grade ovarian cancer who will receive PARP inhibitors.

Full description

A prospective-retrospective analysis of patients with histologically confirmed high grade ovarian cancer who will receive or received olaparib or niraparib will be conducted at any line of treatment.

Enrollment

150 estimated patients

Sex

Female

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • women >18 years old with advanced high grade ovarian cancer

Exclusion criteria

Trial design

150 participants in 1 patient group

One cohort
Description:
women with advanced epithelial ovarian cancer who received PARP inhibitors at any line of treatment
Treatment:
Drug: PARP inhibitor

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems