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
- Diseases
- Prostate cancer
- 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
Sites (36)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.