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ACTIVE NOT RECRUITING
NCT05918042

A Non-interventional Prospective Study of 1-st Line Treatment Approaches in OVArian Cancer Patients With HRD+ Status in Russian Federation

Sponsor: AstraZeneca

View on ClinicalTrials.gov

Summary

Study population will consist of HRD+ (BRCAm +/- positive genomic instability score according to used test system) OC with available medical history. It is estimated that approximately 400 patients will be enrolled in approximately 25 sites. Demographic and clinical characteristics, treatment approaches and outcomes in HRD+ patients with high-grade epithelial ovarian, primary peritoneal, and/or fallopian tube cancer will be collected at baseline and on prospective visits.

Official title: Multicentre, Non-interventional, Observational, Prospective Study to Evaluate 1-st Line Treatment Approaches in HRD+ Ovarian Cancer Patients in Russian Federation

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

400

Start Date

2023-06-21

Completion Date

2025-07-31

Last Updated

2025-07-03

Healthy Volunteers

No

Conditions

Locations (24)

Research Site

Arkhangelsk, Russia

Research Site

Barnaul, Russia

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Chelyabinsk, Russia

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Grozny, Russia

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Irkutsk, Russia

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Izhevsk, Russia

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Kaliningrad, Russia

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Kaluga, Russia

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Krasnodar, Russia

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Krasnoyarsk, Russia

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Lyubertcy, Russia

Research Site

Moscow, Russia

Research Site

N.Novgorod, Russia

Research Site

Nal'chik, Russia

Research Site

Novosibirsk, Russia

Research Site

Omsk, Russia

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Saint Petersburg, Russia

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Saratov, Russia

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Sochi, Russia

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Tomsk, Russia

Research Site

Ufa, Russia

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Vladivostok, Russia

Research Site

Yakutiya, Russia

Research Site

Yaroslavl, Russia