Prostate Cancer Clinical Trial
Official title:
Monitoring Tolerance, Safety and Acceptance of Depo-Eligard® in an Open Label, Retrospective, Non-interventional Clinical Trial
Study will evaluate the real-world effectiveness of Depo-Eligard® after six months of treatment
The study will provide data on the tolerance, safety and acceptance of Depo-Eligard®
(leuproreline acetate) when used in routine clinical practice. Data on efficacy parameters
such as testosterone, PSA levels, symptoms and treatment failure, if available will be
collected.It will reflect the way Depo-Eligard® is used in routine clinical practice and how
PSA, testosterone levels, symptoms and treatment failure, are used as parameters in the
treatment for Prostate Cancer.
Patient data will be collected after a treatment period of six months.
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Observational Model: Cohort, Time Perspective: Retrospective
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