Real-world experience of patients with advanced prostate cancer treated with olaparib and abiraterone
A Prospective Observational Study to Evaluate Real-world Clinical Outcomes and Characteristics of Patients With mCRPC Treated With Olaparib + Abiraterone
This study looks at how well the combination of olaparib and abiraterone works for men with advanced prostate cancer who have or haven't been treated with other hormone therapies before.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 250 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | AstraZeneca Industry-sponsored |
| Locations | 34 sites (Aschaffenburg and 33 other locations) |
| Trial ID | NCT06380738 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather real-world clinical data on patients with metastatic castration-resistant prostate cancer (mCRPC) who are treated with a combination of olaparib and abiraterone. It will assess clinical outcomes in patients who are either naive or previously exposed to novel hormonal agents before starting this treatment. The study will collect demographic and clinical characteristics, as well as treatment history, over a maximum enrollment period of two years, with follow-up extending one year after the last patient is enrolled.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older with documented metastatic castration-resistant prostate cancer who are starting treatment with olaparib and abiraterone.
Not a fit: Patients currently participating in a clinical trial with an investigational prostate cancer treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness and safety of olaparib combined with abiraterone for patients with mCRPC.
How similar studies have performed: While this study is observational and builds on existing treatments, similar approaches have shown promise in other studies involving mCRPC treatments.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Patients participating in a clinical trial with an investigational prostate cancer treatment within 30 days prior to olaparib initiation
Where this trial is running
Aschaffenburg and 33 other locations
- Research Site — Aschaffenburg, Germany (Recruiting)
- Research Site — Augsburg, Germany (Recruiting)
- Research Site — Bergisch Gladbach, Germany (Recruiting)
- Research Site — Berlin, Germany (Recruiting)
- Research Site — Bonn, Germany (Recruiting)
- Research Site — Cologne, Germany (Recruiting)
- Research Site — Dresden, Germany (Recruiting)
- Research Site — Duisburg, Germany (Recruiting)
- Research Site — Eisenach, Germany (Recruiting)
- Research Site — Eisleben Lutherstadt, Germany (Recruiting)
- Research Site — Frankfurt, Germany (Recruiting)
- Research Site — Greifswald, Germany (Recruiting)
- Research Site — Halle, Germany (Recruiting)
- Research Site — Hamburg, Germany (Recruiting)
- Research Site — Hanover, Germany (Recruiting)
- Research Site — Heidelberg, Germany (Recruiting)
- Research Site — Heinsberg, Germany (Recruiting)
- Research Site — Herzogenaurach, Germany (Recruiting)
- Research Site — Leipzig, Germany (Recruiting)
- Research Site — Lübeck, Germany (Recruiting)
- Research Site — Lüneburg, Germany (Recruiting)
- Research Site — Magdeburg, Germany (Recruiting)
- Research Site — Marburg, Germany (Recruiting)
- Research Site — Mülheim, Germany (Recruiting)
- Research Site — Münster, Germany (Recruiting)
- Research Site — Neunkirchen, Germany (Recruiting)
- Research Site — Nuremberg, Germany (Recruiting)
- Research Site — Rüsselsheim am Main, Germany (Recruiting)
- Research Site — Saalfeld, Germany (Recruiting)
- Research Site — Speyer, Germany (Recruiting)
- Research Site — Trier, Germany (Recruiting)
- Research Site — Tübingen, Germany (Recruiting)
- Research Site — Westerstede, Germany (Recruiting)
- Research Site — Wetzlar, Germany (Recruiting)
Study contacts
- Study coordinator: AstraZeneca Clinical Study Information Center
- Email: information.center@astrazeneca.com
- Phone: 1-877-240-9479
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.