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NCT06242392

The Correlation Between HRD Detection and the Efficacy of PARP Inhibitors in Ovarian Cancer

Not yet recruiting Last updated 5 February 2024
What this trial tests

trial testing homologous recombination deficiency in Ovarian Neoplasms in 250 participants. Not yet recruiting.

Timeline
31 January 2024
Primary endpoint
1 May 2026
1 July 2026

Quick facts

Lead sponsorFujian Cancer Hospital
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment250
Start date31 January 2024
Primary completion1 May 2026
Estimated completion1 July 2026

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Cancer Hospital

Who can join

18 and older, female only, with Ovarian Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Clinicopathological data were collected from ovarian cancer patients treated with PARP inhibitors, with follow-up imaging conducted before and after treatment. The efficacy was evaluated according to RECIST criteria, comparing the correlation between different HRD statuses and the efficacy of PARP inhibitors in ovarian cancer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Ovarian Neoplasms

Currently open trials in the same condition.

Other Fujian Cancer Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06242392.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing