Navigant Study- Treatment Patterns in mCRPC (Metastatic Castrate Resistant Prostate Cancer )
Completed
Conditions studied: Prostatic Neoplasms, Castration-Resistant
In brief
Categorize the clinical parameters and patient determinants that drive physician decision making for treatment selection including Radium-223 for patients with mCRPC.
Key facts
- Study ID
- NCT02899104
- Run by
- Bayer
- People needed
- 200
- Starts
- 2017-06-15
- Expected to finish
- 2019-03-31
- Last updated by the study team
- 2020-03-31
Who can join
Age: 18 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Patients were diagnosed with bone metastatic castration-resistant prostate cancer (mCRPC) per medical chart.
- Patients were at least 18 years of age as of the first diagnosis for mCRPC.
- Patients must have received at least one intravenous injection of Radium-223 (Xofigo).
- First injection of Radium-223 must have started between periods
- 1-January-2014 to 30-June-2014 or 15-November-2014 to present.
- Patients must have a minimum of 12 months documented follow-up records following last Radium-223 treatment or death within 12 months of last dose.
You may not qualify if…
- Patients who received Radium-223 as part in an interventional clinical trial
- Actively treated, or expect to be treated, in 6 months before last follow-up, for any other malignancy with the exception of non-metastatic skin cancer or low-grade superficial bladder cancer.
Where it is running
- Whippany — Whippany, New Jersey, United States
Full record on ClinicalTrials.gov
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