RecruitingNCT07146113

Treatment Approaches and Biomarkers PRevalence In de Novo MEtastatic Hormone-sensitive Prostate Cancer in Russian Federation

A Multicentre Observational Study on Treatment Approaches and Biomarkers in de Novo Metastatic Hormone Sensitive Prostate Cancer in Russian Federation


Sponsor

AstraZeneca

Enrollment

400 participants

Start Date

Jun 30, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

A multicentre observational study on treatment approaches and biomarkers in de novo metastatic hormone sensitive prostate cancer in Russian Federation


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria7

  • Male patients aged ≥ 18 years old;
  • Signed ICF, including consent for FFPE tumor tissue sample testing;
  • De novo histologically confirmed high-aggressive (Gleason 8-10) mPC;
  • Diagnosis of mPC (metastatic prostate cancer) within 2 years prior to inclusion;
  • Availability of source medical documentation;
  • Presence of biopsy FFPE tumor tissue sample, obtained as part of standard clinical practice, which will be used for biomarker testing;
  • Unknown HRRm status.

Exclusion Criteria1

  • \. Participation in any interventional trial since the mPC diagnosis.

Locations(17)

Research Site

Arkhangelsk, Russia

Research Site

Barnaul, Russia

Research Site

Chelyabinsk, Russia

Research Site

Irkutsk, Russia

Research Site

Krasnodar, Russia

Research Site

Krasnoyarsk, Russia

Research Site

Moscow, Russia

Research Site

Moscow, Russia

Research Site

Nizhny Novgorod, Russia

Research Site

Obninsk, Russia

Research Site

Omsk, Russia

Research Site

Saint Petersburg, Russia

Research Site

Saransk, Russia

Research Site

Tomsk, Russia

Research Site

Tyumen, Russia

Research Site

Ufa, Russia

Research Site

Yekaterinburg, Russia

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NCT07146113


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