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NCT06380738Active, not recruiting

Real-World Clinical Experience of Patients With Metastatic Castration-Resistant Prostate Cancer Treated With Olaparib + Abiraterone (PROceed)

A Prospective Observational Study to Evaluate Real-world Clinical Outcomes and Characteristics of Patients With mCRPC Treated With Olaparib + Abiraterone

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

PROceed is a multisite, prospective, observational study that describes the real-world use and clinical experience of mCRPC patients treated with the combination of olaparib and abiraterone in the mCRPC setting. Clinical outcomes will be assessed in patients who are either NHA-naive or NHA-exposed prior to initiating olaparib + abiraterone treatment, respectively. Patient demographic and clinical characteristics, as well as treatment received prior and subsequent to olaparib + abiraterone, will also be described. The study plans to enroll patients for a maximum of 2 years and follow up patients from initiation of olaparib until 1 year post last patient in.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
111 (actual)
First submitted
1 Feb 2024
Start date
14 Feb 2024
Primary completion date
14 Feb 2027
Lead sponsor
AstraZeneca
NCT number
NCT06380738

What you commit to

  • Study type: Observational
  • Participants enrolled: 111
  • From 14 Feb 2024 to the primary completion date, 14 Feb 2027
  • 36 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients participating in a clinical trial with an investigational prostate cancer treatment within 30 days prior to olaparib initiation

Who the study is looking for

  • Willing and able to provide written informed consent;
  • 18 years of age and above;
  • Documented histopathology or cytopathology of PCa, adenocarcinoma;
  • Confirmed as mCRPC;
  • Initiated olaparib + abiraterone after site activation

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (36)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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AschaffenburgGermanyUnknown status
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AugsburgGermanyUnknown status
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Bergisch GladbachGermanyUnknown status
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BerlinGermanyUnknown status
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BonnGermanyUnknown status
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CologneGermanyUnknown status
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DresdenGermanyUnknown status
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DuisburgGermanyUnknown status
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EisenachGermanyUnknown status
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Eisleben LutherstadtGermanyUnknown status
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FrankfurtGermanyUnknown status
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GreifswaldGermanyUnknown status
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HalleGermanyUnknown status
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HamburgGermanyUnknown status
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HanoverGermanyUnknown status
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HeidelbergGermanyUnknown status
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HeinsbergGermanyUnknown status
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HerzogenaurachGermanyUnknown status
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LeipzigGermanyUnknown status
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LichtenfelsGermanyUnknown status
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LübeckGermanyUnknown status
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LüneburgGermanyUnknown status
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MagdeburgGermanyUnknown status
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MarburgGermanyUnknown status
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MülheimGermanyUnknown status
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MünsterGermanyUnknown status
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NurembergGermanyUnknown status
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Rüsselsheim am MainGermanyUnknown status
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SaalfeldGermanyUnknown status
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SpeyerGermanyUnknown status
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TrierGermanyUnknown status
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TübingenGermanyUnknown status
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WesterstedeGermanyUnknown status
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WetzlarGermanyUnknown status
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WinnendenGermanyUnknown status
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WuppertalGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.